Senior Principal Mechanical Engineer (Permanent) Location: United Kingdom Region: Cheshire Salary: £50-70k Type: Permanent, Full Time Description As a subject matter expert in the field of design and development of medical device or combination products, you will be responsible for ensuring that projects and programs, primarily injection device development projects, are delivered according to best engineering practice. You will have state-of-the-art knowledge of the regulations, directives, guidelines and standards, engineering practises, tools and technologies relevant to the development of medical devices and combination products. Your creativity, knowledge and experience will enable you to identify and to resolve complex engineering problems and to anticipate, and hence to avoid, problems before they develop. As a specialist in the field of medical device and combination product development, you will also be responsible for managing external engineering resources and for supporting and mentoring other members of the Engineering Team. You will also play a leading role in the development and maintenance of departmental operating systems and processes. Duties Assemble and lead engineering teams from within the SDT and, if required, from external suppliers, to deliver the activities and achieve project and departmental objectives. Ensure that products for which you are responsible are: o robust in design through the application of appropriate engineering design and analysis, verified by the provision of objective evidence of reliability, safety and efficacy. o conducted in compliance with SDT's Quality Management System. Manage relationships with contract design houses, contract manufacturing companies and specialist external suppliers. Lead the engineering aspects of device safety risk management, such as design and process FMEA. Represent SDT in internal and external audits. Perform the role of independent project reviewer for device development projects in which you are not directly involved. Support the Engineering Manager in recruitment activities. Play a leading role in the continuous improvement of departmental practises: o Support development of Standard Operating Procedures, guidelines and templates. o Coaching and mentoring of Engineering team members and colleagues up to the level of Principal Engineer. Travel globally as required to support the projects, up to 25% of time out of the office. Travel might include visiting suppliers' facilities or manufacturing sites. Contribute to the development of SDT's device strategy. Skills Graduate in Engineering, Scientific or other Technical discipline. At least 10 years relevant industry experience in product development, from concept to commercialisation. Previous experience in the design, manufacture and life-cycle management of medical device or combination products (preferred, or significant specialist expertise from another relevant industry). Recognized as an engineering authority within the organization, both within and beyond SDT. Knowledge of Solidworks 3D CAD (preferred). Specialist problem solving ability to find solutions to problems encountered with developing mechanical systems and manufacturing processes. Exhibits ingenuity, creativity and resourcefulness. Applies knowledge of highly advanced technologies, scientific principles, theories and concepts. Competent in the use of statistical methods, for example for the determination of design input requirements, verification and validation testing. Advanced skills in mentoring and coaching skills, including coaching of colleagues of senior and principal levels. Competencies Trusted to operate independently, with minimal guidance required. Provides project leadership with confidence, gravitas and charisma. Is looked to by the Engineering team for direction. Aptitude for working in a team environment and operating outside remit to meet deadlines when necessary. Ability to influence and educate at all levels. Confident in own judgement. Prepared to take difficult decisions and able to persuade others. Where appropriate, willing to challenge the status quo. Adaptable, cooperative and helpful attitude towards colleagues and customers while always acting with integrity. Analytical engineering assessment of mechanisms and systems. Good verbal and written communication including high quality engineering documentation. Enjoys working hard, is driven and able to challenge. Can effectively cope with change, coping with risk and uncertainty while comfortably adapting to changing conditions. Remains positive through adversity. Relationships Interfaces with, and influences, numerous other business units, including legal, commercial, drug development, operations regulatory and procurement. In situations where engineering activities are contracted out to third parties, will be responsible for interfacing with these external suppliers as well as assessing and approving their output. Reporting to the Engineering Manager, who reports to the Head of SDT. SDT is part of the Global R&D Innovation Technology business unit.
Jun 23, 2018
Senior Principal Mechanical Engineer (Permanent) Location: United Kingdom Region: Cheshire Salary: £50-70k Type: Permanent, Full Time Description As a subject matter expert in the field of design and development of medical device or combination products, you will be responsible for ensuring that projects and programs, primarily injection device development projects, are delivered according to best engineering practice. You will have state-of-the-art knowledge of the regulations, directives, guidelines and standards, engineering practises, tools and technologies relevant to the development of medical devices and combination products. Your creativity, knowledge and experience will enable you to identify and to resolve complex engineering problems and to anticipate, and hence to avoid, problems before they develop. As a specialist in the field of medical device and combination product development, you will also be responsible for managing external engineering resources and for supporting and mentoring other members of the Engineering Team. You will also play a leading role in the development and maintenance of departmental operating systems and processes. Duties Assemble and lead engineering teams from within the SDT and, if required, from external suppliers, to deliver the activities and achieve project and departmental objectives. Ensure that products for which you are responsible are: o robust in design through the application of appropriate engineering design and analysis, verified by the provision of objective evidence of reliability, safety and efficacy. o conducted in compliance with SDT's Quality Management System. Manage relationships with contract design houses, contract manufacturing companies and specialist external suppliers. Lead the engineering aspects of device safety risk management, such as design and process FMEA. Represent SDT in internal and external audits. Perform the role of independent project reviewer for device development projects in which you are not directly involved. Support the Engineering Manager in recruitment activities. Play a leading role in the continuous improvement of departmental practises: o Support development of Standard Operating Procedures, guidelines and templates. o Coaching and mentoring of Engineering team members and colleagues up to the level of Principal Engineer. Travel globally as required to support the projects, up to 25% of time out of the office. Travel might include visiting suppliers' facilities or manufacturing sites. Contribute to the development of SDT's device strategy. Skills Graduate in Engineering, Scientific or other Technical discipline. At least 10 years relevant industry experience in product development, from concept to commercialisation. Previous experience in the design, manufacture and life-cycle management of medical device or combination products (preferred, or significant specialist expertise from another relevant industry). Recognized as an engineering authority within the organization, both within and beyond SDT. Knowledge of Solidworks 3D CAD (preferred). Specialist problem solving ability to find solutions to problems encountered with developing mechanical systems and manufacturing processes. Exhibits ingenuity, creativity and resourcefulness. Applies knowledge of highly advanced technologies, scientific principles, theories and concepts. Competent in the use of statistical methods, for example for the determination of design input requirements, verification and validation testing. Advanced skills in mentoring and coaching skills, including coaching of colleagues of senior and principal levels. Competencies Trusted to operate independently, with minimal guidance required. Provides project leadership with confidence, gravitas and charisma. Is looked to by the Engineering team for direction. Aptitude for working in a team environment and operating outside remit to meet deadlines when necessary. Ability to influence and educate at all levels. Confident in own judgement. Prepared to take difficult decisions and able to persuade others. Where appropriate, willing to challenge the status quo. Adaptable, cooperative and helpful attitude towards colleagues and customers while always acting with integrity. Analytical engineering assessment of mechanisms and systems. Good verbal and written communication including high quality engineering documentation. Enjoys working hard, is driven and able to challenge. Can effectively cope with change, coping with risk and uncertainty while comfortably adapting to changing conditions. Remains positive through adversity. Relationships Interfaces with, and influences, numerous other business units, including legal, commercial, drug development, operations regulatory and procurement. In situations where engineering activities are contracted out to third parties, will be responsible for interfacing with these external suppliers as well as assessing and approving their output. Reporting to the Engineering Manager, who reports to the Head of SDT. SDT is part of the Global R&D Innovation Technology business unit.
Penguin Recruitment Ltd
Sheffield, South Yorkshire, UK
NE61320 Engineering Geologist - Sheffield- £competitive Our Client have a requirement for an Engineering Geologist in their Sheffield office. Due to continued success and expansion our clients are looking for experienced Engineering Geologists to join them. You will be working on a range of projects..... click apply for full job details
Jun 23, 2018
Full time
NE61320 Engineering Geologist - Sheffield- £competitive Our Client have a requirement for an Engineering Geologist in their Sheffield office. Due to continued success and expansion our clients are looking for experienced Engineering Geologists to join them. You will be working on a range of projects..... click apply for full job details
An exciting opportunity has arisen for a motivated, enthusiastic, and creative Mathematical Physicist to work in the product development team of an innovative and growing Technology company at their site in the North East of England. In this role you will apply physical and mathematical skills to projects for clients in the Oil, Gas and Chemicals industries. The successful candidate will be involved in delivering insights from unstructured process plant data and working closely with clients to bring real value to their processes. They will also design, model and conduct experiments, build prototypes and be involved in field trials for novel industrial sensors. Interested candidates should hold a PhD or Master's degree in Physics or Applied Maths, the successful candidate will be a creative thinker who can demonstrate prior success in the application of physics and data analysis skills as well as an enthusiasm for the role and an acute mind for problem solving. Alongside your academic achievements being able to demonstrate further understanding in the fields of mathematics, statistics, physics or computer science would be advantageous. Prior industrial/internships/project experience is also strongly recommended. Candidates should possess excellent mathematical and programming skills. o Capable of working with large quantities of unstructured data and delivering meaningful results to customers. o Experience in applying statistics and signal analysis to real work problems. o Experience in analysing data with MATLAB, Python or R etc. o Experience in working with Neural Networks and Machine Learning to understand complex data sets. o Experience in working with Microsoft Azure cloud services preferable. o Experience in analysing industrial data sets preferable. Possess solid experimental skills o Capable of designing and performing experiments to test ideas. o Capable of finding practical engineering solutions. Have good people and leadership skills o Able to interact with customers to understand where we can add value to their operations. o Able to interact with the development team and wider business to solve problems. If you are interested in applying to this role and would like further information please feel free to contact Graham at CY Partners. Please note that if you have not been contacted within 5 business days you have been unsuccessful in your application.
Jun 23, 2018
An exciting opportunity has arisen for a motivated, enthusiastic, and creative Mathematical Physicist to work in the product development team of an innovative and growing Technology company at their site in the North East of England. In this role you will apply physical and mathematical skills to projects for clients in the Oil, Gas and Chemicals industries. The successful candidate will be involved in delivering insights from unstructured process plant data and working closely with clients to bring real value to their processes. They will also design, model and conduct experiments, build prototypes and be involved in field trials for novel industrial sensors. Interested candidates should hold a PhD or Master's degree in Physics or Applied Maths, the successful candidate will be a creative thinker who can demonstrate prior success in the application of physics and data analysis skills as well as an enthusiasm for the role and an acute mind for problem solving. Alongside your academic achievements being able to demonstrate further understanding in the fields of mathematics, statistics, physics or computer science would be advantageous. Prior industrial/internships/project experience is also strongly recommended. Candidates should possess excellent mathematical and programming skills. o Capable of working with large quantities of unstructured data and delivering meaningful results to customers. o Experience in applying statistics and signal analysis to real work problems. o Experience in analysing data with MATLAB, Python or R etc. o Experience in working with Neural Networks and Machine Learning to understand complex data sets. o Experience in working with Microsoft Azure cloud services preferable. o Experience in analysing industrial data sets preferable. Possess solid experimental skills o Capable of designing and performing experiments to test ideas. o Capable of finding practical engineering solutions. Have good people and leadership skills o Able to interact with customers to understand where we can add value to their operations. o Able to interact with the development team and wider business to solve problems. If you are interested in applying to this role and would like further information please feel free to contact Graham at CY Partners. Please note that if you have not been contacted within 5 business days you have been unsuccessful in your application.
3R Consulting Ltd
Chester, Cheshire West and Chester, UK
3R Consulting are recruiting an Analytical Development Scientist responsible for production & testing of products related to feasibility method development, QC release and stability studies for a leading scientific company; You will develop & validate robust analytical test methods to support formulation development, cleaning verification, stability & quality ensuring delivery in accordance with project timescales & deadlines. You will perform analytical tests on raw materials, in-process, finished products (QC) and stability samples & perform statistical analysis & interpretation of data. You will report any deviations and assist in investigations including completion of CAPA. You will assist with day to day running of the laboratory, performing stock control, house cleaning, waste disposal and work with management to identify, develop & implement new working practices and complete and review laboratory documentation.. You must be experienced of working in a multi disciplinary team with the ability to plan, execute and deliver practical investigations on time against pre-defined protocols. You will have a BSc or equivalent in Chemist or related subject, at least one year experience of HPLC analysis & method development. Knowledge & experience within a pharmaceutical product/chemical development environment and an understanding of the drug development process To apply for the position please forward your CV to the recruiter below:
Jun 23, 2018
3R Consulting are recruiting an Analytical Development Scientist responsible for production & testing of products related to feasibility method development, QC release and stability studies for a leading scientific company; You will develop & validate robust analytical test methods to support formulation development, cleaning verification, stability & quality ensuring delivery in accordance with project timescales & deadlines. You will perform analytical tests on raw materials, in-process, finished products (QC) and stability samples & perform statistical analysis & interpretation of data. You will report any deviations and assist in investigations including completion of CAPA. You will assist with day to day running of the laboratory, performing stock control, house cleaning, waste disposal and work with management to identify, develop & implement new working practices and complete and review laboratory documentation.. You must be experienced of working in a multi disciplinary team with the ability to plan, execute and deliver practical investigations on time against pre-defined protocols. You will have a BSc or equivalent in Chemist or related subject, at least one year experience of HPLC analysis & method development. Knowledge & experience within a pharmaceutical product/chemical development environment and an understanding of the drug development process To apply for the position please forward your CV to the recruiter below:
Job Description Multilingual Medical Information Officer (Swedish) Home Working Position Full-time Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes. Job Description Essential Functions Include: 1. Medical Information service delivery • Providing a high quality medical information enquiry handling service by answering technical questions in respect of designated products in an accurate, confident and professional manner. Enquiries may be received via phone, letter, email and fax. • Complying with the specific Working Practices (WPs) which have been agreed with designated clients as well as following processes which may be documented in Client Instructions/other documentation. • Ensuring that tasks are completed within the deadlines documented in the agreed ProPharma Group SOPs and WPs. • Recognising adverse events and defective product reports and handling and reporting these in strict compliance with agreed ProPharma Group SOPs and WPs. • Translating English documents into the target language or vice versa, and delivering these translated responses either on the phone or in writing. • Using existing standard responses to prepare medical information correspondence (via client databases) or taking responsibility for liaising with the Medical Information Support Services (MISS) department to request the generation of medical information correspondence. • Logging all enquiries handled in an accurate, comprehensive and timely fashion in to Enquiry Handling Systems. • Liaising with Medical Information Assistants to ensure data received from clients is saved on file in a timely manner where applicable. • Ensuring that any confidential information or personal data related to ProPharma Group and its clients is managed in accordance with Data Privacy regulations as described in ProPharma Group SOPs. • Maintaining awareness of, and ensuring compliance with, the legal requirements and professional guidelines associated with the provision of medical information on behalf of the Pharmaceutical Industry. 2. Quality Assurance • Maintaining quality in all areas of the job, particularly reporting of Adverse Events, Product Quality Complaints and logging enquiries into Enquiry Handling Systems. • Performing quality checks on Adverse Events, Product Quality Complaints, correspondence to ensure accuracy in all areas of the job. • Quality checking translations in line with the translation SOP. 3. General • Performing additional tasks within the Company as delegated by the Manager. • Having a good working knowledge of, and to comply with, the SOPs of ProPharma Group. • Complying with the Company's health and safety policies. • Ensuring the Confidentiality Statement within the Contract of Employment is adhered to at all times in respect of the data and property of ProPharma Group, its clients and employees of the business. Qualifications 1. A degree in a life science or pharmacy, or equivalent. 2. Mother tongue in target language. 3. Fluent in English. 4. Strong translation skills. 5. Able to work within a team in an open and professional manner. 6. Excellent written and oral communication skills and computer literacy. 7. Sound planning, prioritising and organisational skills. Showing an effective workload management system and meeting deadlines. 8. Able to take responsibility for work allocated (ensuring tasks are followed through to completion). 9. Accuracy and attention to detail. 10. Able to understand and follow processes. Additional Information All candidates must be legally eligible to work in the United Kingdom and any offer of employment will be subject to the candidate having a personal non-shared telephone line and broadband available and connected at their own home. We require download speed of 5.0 or above and upload speed of 1.0 and above We are an equal opportunity employer. M/F/D/V ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
Jun 23, 2018
Full time
Job Description Multilingual Medical Information Officer (Swedish) Home Working Position Full-time Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes. Job Description Essential Functions Include: 1. Medical Information service delivery • Providing a high quality medical information enquiry handling service by answering technical questions in respect of designated products in an accurate, confident and professional manner. Enquiries may be received via phone, letter, email and fax. • Complying with the specific Working Practices (WPs) which have been agreed with designated clients as well as following processes which may be documented in Client Instructions/other documentation. • Ensuring that tasks are completed within the deadlines documented in the agreed ProPharma Group SOPs and WPs. • Recognising adverse events and defective product reports and handling and reporting these in strict compliance with agreed ProPharma Group SOPs and WPs. • Translating English documents into the target language or vice versa, and delivering these translated responses either on the phone or in writing. • Using existing standard responses to prepare medical information correspondence (via client databases) or taking responsibility for liaising with the Medical Information Support Services (MISS) department to request the generation of medical information correspondence. • Logging all enquiries handled in an accurate, comprehensive and timely fashion in to Enquiry Handling Systems. • Liaising with Medical Information Assistants to ensure data received from clients is saved on file in a timely manner where applicable. • Ensuring that any confidential information or personal data related to ProPharma Group and its clients is managed in accordance with Data Privacy regulations as described in ProPharma Group SOPs. • Maintaining awareness of, and ensuring compliance with, the legal requirements and professional guidelines associated with the provision of medical information on behalf of the Pharmaceutical Industry. 2. Quality Assurance • Maintaining quality in all areas of the job, particularly reporting of Adverse Events, Product Quality Complaints and logging enquiries into Enquiry Handling Systems. • Performing quality checks on Adverse Events, Product Quality Complaints, correspondence to ensure accuracy in all areas of the job. • Quality checking translations in line with the translation SOP. 3. General • Performing additional tasks within the Company as delegated by the Manager. • Having a good working knowledge of, and to comply with, the SOPs of ProPharma Group. • Complying with the Company's health and safety policies. • Ensuring the Confidentiality Statement within the Contract of Employment is adhered to at all times in respect of the data and property of ProPharma Group, its clients and employees of the business. Qualifications 1. A degree in a life science or pharmacy, or equivalent. 2. Mother tongue in target language. 3. Fluent in English. 4. Strong translation skills. 5. Able to work within a team in an open and professional manner. 6. Excellent written and oral communication skills and computer literacy. 7. Sound planning, prioritising and organisational skills. Showing an effective workload management system and meeting deadlines. 8. Able to take responsibility for work allocated (ensuring tasks are followed through to completion). 9. Accuracy and attention to detail. 10. Able to understand and follow processes. Additional Information All candidates must be legally eligible to work in the United Kingdom and any offer of employment will be subject to the candidate having a personal non-shared telephone line and broadband available and connected at their own home. We require download speed of 5.0 or above and upload speed of 1.0 and above We are an equal opportunity employer. M/F/D/V ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
Division: Clinical R&D Operations Job Function Summary Overview: This individual will provide support to the clinical study staff within the Clinical R&D COE, as well as fostering strong, productive relationships with colleagues within the Clinical R&D COE organization. Responsible for processing, tracking, and filing of study documents, and management of the Trial Master File within the clinical projects. In addition, administratively support clinical study staff as required. Supports project managers within the assigned clinical studies. Key Job Activities: Clinical Administration Tasks - (includes CTMS build and tracking, v-TMF build & upload) • Under general supervision, accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions. • Creation/distribution of regulatory binders & the wet-ink signed documents binder • Assist study staff and investigators to quickly and effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File). Respond to problems and assists in implementing corrective and preventive actions. • Assist in providing internal communication of important clinical data and events. • Support ongoing use of CTMS by maintaining and tracking relevant activities. • Provide safety documentation to other functional groups in support of safety committee meetings as requested (supporting role). Other Administrative Tasks • May be asked to provide support for study supplies creation, ordering and distribution to the sites e.g. print protocols, burn DVDs • May be asked to assist with Device tracking and ordering if required and if applicable. • Assistance with logistics for Investigator meetings/expert panel meetings • Assistance with distribution of newsletter (create mailing list from CTMS and routing for internal approval) • Participates in process improvement activities related to CTMS/v-TMF within the department. Job Qualifications Education • Minimum of a Bachelor's Degree is required. Experience • Previous clinical research experience a plus. • Requires previous administrative support experience or equivalent for at least 1 year. • Clinical/medical background a plus. Knowledge • Requires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point). Additional Requirements Demonstrated competencies in the following areas are required: o Tracking o Written and verbal communications o Attention to details o Organizational skills
Jun 23, 2018
Division: Clinical R&D Operations Job Function Summary Overview: This individual will provide support to the clinical study staff within the Clinical R&D COE, as well as fostering strong, productive relationships with colleagues within the Clinical R&D COE organization. Responsible for processing, tracking, and filing of study documents, and management of the Trial Master File within the clinical projects. In addition, administratively support clinical study staff as required. Supports project managers within the assigned clinical studies. Key Job Activities: Clinical Administration Tasks - (includes CTMS build and tracking, v-TMF build & upload) • Under general supervision, accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions. • Creation/distribution of regulatory binders & the wet-ink signed documents binder • Assist study staff and investigators to quickly and effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File). Respond to problems and assists in implementing corrective and preventive actions. • Assist in providing internal communication of important clinical data and events. • Support ongoing use of CTMS by maintaining and tracking relevant activities. • Provide safety documentation to other functional groups in support of safety committee meetings as requested (supporting role). Other Administrative Tasks • May be asked to provide support for study supplies creation, ordering and distribution to the sites e.g. print protocols, burn DVDs • May be asked to assist with Device tracking and ordering if required and if applicable. • Assistance with logistics for Investigator meetings/expert panel meetings • Assistance with distribution of newsletter (create mailing list from CTMS and routing for internal approval) • Participates in process improvement activities related to CTMS/v-TMF within the department. Job Qualifications Education • Minimum of a Bachelor's Degree is required. Experience • Previous clinical research experience a plus. • Requires previous administrative support experience or equivalent for at least 1 year. • Clinical/medical background a plus. Knowledge • Requires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point). Additional Requirements Demonstrated competencies in the following areas are required: o Tracking o Written and verbal communications o Attention to details o Organizational skills
Penguin Recruitment Ltd
Birmingham, Birmingham, West Midlands, UK
CDM Consultant - Multi-Disciplinary Client - Nottinghamshire £40,000 - £50,000 + Benefits My client is a multi-disciplinary consultancy, operating across the UK, Australia, Asia and Europe. Employing more than 800 people at 20 locations across the globe, they have established themselves as knowledgeable and award winning..... click apply for full job details
Jun 23, 2018
Full time
CDM Consultant - Multi-Disciplinary Client - Nottinghamshire £40,000 - £50,000 + Benefits My client is a multi-disciplinary consultancy, operating across the UK, Australia, Asia and Europe. Employing more than 800 people at 20 locations across the globe, they have established themselves as knowledgeable and award winning..... click apply for full job details
About the Company: Our well established client is looking for a Site and Laboratory Technician to join their busy team in Derby Key Responsibilities: · Performing site sampling and carrying out testing procedures with minimal supervision · Ensuring that all work is carried out to the highest standards. · Maintaining good laboratory practice and maintenance of laboratory and site equipment and safe working procedures · Ensuring that adequate and proper records are kept to satisfy the UKAS requirements · To ensure that all test equipment is regularly checked, calibrated and functioning properly · Produce test results in-line with the expectations of the Laboratory Supervisor and work to the test deadlines and targets as instructed. · Experience carrying out plate load testing, CBR, in situ density testing and basic soils laboratory testing would be an advantage, but not mandatory as for the right candidates full training would be given About you: · Full UK Driving License · A valid CSCS card would be advantageous · Good communication skills both verbal and written · Computer literate · Overtime and some weekend work will be required What's in it for you? · Salary £18,000 - £20,000 depending on experience · Contributory Pension Scheme after probationary period · Overtime paid for hours over the basic 38.75 hour week ·Full on the job training will be given ·Potential for progression for the right applicant
Jun 23, 2018
About the Company: Our well established client is looking for a Site and Laboratory Technician to join their busy team in Derby Key Responsibilities: · Performing site sampling and carrying out testing procedures with minimal supervision · Ensuring that all work is carried out to the highest standards. · Maintaining good laboratory practice and maintenance of laboratory and site equipment and safe working procedures · Ensuring that adequate and proper records are kept to satisfy the UKAS requirements · To ensure that all test equipment is regularly checked, calibrated and functioning properly · Produce test results in-line with the expectations of the Laboratory Supervisor and work to the test deadlines and targets as instructed. · Experience carrying out plate load testing, CBR, in situ density testing and basic soils laboratory testing would be an advantage, but not mandatory as for the right candidates full training would be given About you: · Full UK Driving License · A valid CSCS card would be advantageous · Good communication skills both verbal and written · Computer literate · Overtime and some weekend work will be required What's in it for you? · Salary £18,000 - £20,000 depending on experience · Contributory Pension Scheme after probationary period · Overtime paid for hours over the basic 38.75 hour week ·Full on the job training will be given ·Potential for progression for the right applicant
My client, a leading energy company based in Barrow-in-Furnes are currently recruiting for 1 month temporary role within their laboratory to assist in a chemical cleaning project at their plant. Day to day responsibilities. - Conducting routine chemical analysis - Work to ISO 14001 standards - Conduct laboratory trials for decommissioning activities. - Conduct sample analysis of liquids. Are you right for the role? - You will have a HND, HNC or Degree in Chemistry or related subject. - You will have experience conducting laboratory analysis - You will have worked in a chemical sector position previously within analysis/laboratory role. This is an immediate start, therefore please apply today. Reed Specialist Recruitment Limited is an employment agency and employment business
Jun 23, 2018
My client, a leading energy company based in Barrow-in-Furnes are currently recruiting for 1 month temporary role within their laboratory to assist in a chemical cleaning project at their plant. Day to day responsibilities. - Conducting routine chemical analysis - Work to ISO 14001 standards - Conduct laboratory trials for decommissioning activities. - Conduct sample analysis of liquids. Are you right for the role? - You will have a HND, HNC or Degree in Chemistry or related subject. - You will have experience conducting laboratory analysis - You will have worked in a chemical sector position previously within analysis/laboratory role. This is an immediate start, therefore please apply today. Reed Specialist Recruitment Limited is an employment agency and employment business
Quality Specialist - Medical Device A leading healthcare company located in Yorkshire who specialise in the support of disease through advanced technology, now require a Quality Specialist to join them; you will be responsible to lead on all quality related aspects of new product development. The role will involve working with design teams throughout the design process to ensure that requirements of current standards and regulatory requirements are being met. The role: * Collaborate with design project team members to achieve key deliverables to meet project deadlines * Identify, lead and plan on quality related project deliverables * Work with the project teams to plan and organise quality related deliverables and requirements * Participate and lead in project risk analysis (e.g., establishing risk documents such as FMEA) * Work with project teams to select and evaluate suppliers during the design phase * Completion of product development documentation required for the DHF, regulatory submissions, external presentations, quality systems and manufacturing * Review/ carry out gap analysis of existing DHFs/Technical Files to identify testing requirements to comply with current standards * Identify and plan testing strategies for various quality related requirements (eg. sterilisation and cleaning methodologies) * Write technical justifications and validation reports The Candidate: * Candidates will have a degree or equivalent qualification in a science based subject. * Experience of critically assessing technical information literature and data, also writing of technical reports and clinical evaluation reports would be desirable * Good knowledge of Design History File Documents; Plans, Design Inputs, Verification, Validation, Design Reviews, Design Outputs * Experience in the Medical Device industry, working to 93/42/EEC and ISO 13485:2003 standards would be desirable Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age.
Jun 23, 2018
Quality Specialist - Medical Device A leading healthcare company located in Yorkshire who specialise in the support of disease through advanced technology, now require a Quality Specialist to join them; you will be responsible to lead on all quality related aspects of new product development. The role will involve working with design teams throughout the design process to ensure that requirements of current standards and regulatory requirements are being met. The role: * Collaborate with design project team members to achieve key deliverables to meet project deadlines * Identify, lead and plan on quality related project deliverables * Work with the project teams to plan and organise quality related deliverables and requirements * Participate and lead in project risk analysis (e.g., establishing risk documents such as FMEA) * Work with project teams to select and evaluate suppliers during the design phase * Completion of product development documentation required for the DHF, regulatory submissions, external presentations, quality systems and manufacturing * Review/ carry out gap analysis of existing DHFs/Technical Files to identify testing requirements to comply with current standards * Identify and plan testing strategies for various quality related requirements (eg. sterilisation and cleaning methodologies) * Write technical justifications and validation reports The Candidate: * Candidates will have a degree or equivalent qualification in a science based subject. * Experience of critically assessing technical information literature and data, also writing of technical reports and clinical evaluation reports would be desirable * Good knowledge of Design History File Documents; Plans, Design Inputs, Verification, Validation, Design Reviews, Design Outputs * Experience in the Medical Device industry, working to 93/42/EEC and ISO 13485:2003 standards would be desirable Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age.
OrionGroup are looking for a Clinical Research Monitor for our multinational lifesciences client based in the West Yorkshire area on an initial 12-month contract. Please note there will be frequent travel throughout the UK and occasional travel to sites across Europe. SUMMARY OF POSITION: Provide support to the implementation of the clinical research operations programme for all appropriate therapeutic areas for the company in accordance with all applicable regulations for Medical Devices. Plan & implement a programme of monitoring for all international regulatory and post marketing clinical research studies and maintain the highest ethical, clinical and scientific standards ensuring both the safety and well being of all trial participants, and good/rigorous scientific practice. Main Responsibilities of the role Provide support to EMEA Monitoring Resource Manager and act as the lead monitor within the EMEA region. Provide feedback on current and best monitoring practice, procedural and regulatory compliance, and system adoption (e.g. electronic TMF and Clinical Trial Management System (CTMS)). Perform monitor observation visits throughout the EMEA region and provide feedback to EMEA Monitoring Resource Manager. Provide support to Clinical Trial Leader for agreed projects in the EMEA Clinical Research programme for the defined therapeutic area by monitoring and reporting on studies progress in accordance with all Corporate and Statutory requirements to agreed timescales. Maintain the highest ethical, clinical and scientific standards ensuring both the safety and well being of all trial participants and good/rigorous scientific practice. Keep abreast of international legislation and other requirements concerning clinical research. Prepare and submit submissions for the approval of clinical investigations to regulatory authorities and ethics committees. Keep abreast of developments in clinical research and the clinical literature in therapeutic areas of responsibility. Assist in the preparation of consent documentation where required for the proper scientific evaluation of new or existing products in accordance with all ethical and regulatory requirements for Medical Devices in respect of applicable European and International Medical Devices Regulations. Monitor defined clinical studies in accordance with Good Clinical Practice requirements and provide regular feedback to company personnel on the progress of trials. Administer the inventory of Investigational Products and control the issue of investigational products to approved sites where necessary. Participate in project teams and build relationships with investigators, regulatory bodies and appropriate company personnel as required regarding clinical research issues, working as directed by Clinical Trial Leader & monitoring team. Maintain compliance with Company SOPs. Maintain a high standard of housekeeping and filing accuracy. Ideal Background and Skillset of the successful candidate 1st Degree in Life Sciences, Health Sciences or related field to Biomedical Engineering or equivalent combination of education and experience. 5+ years' experience of clinical trials monitoring in a medical company preferably with medical devices. Knowledge of clinical study design and management. Relevant experience in implementation of clinical research studies. Working knowledge of international regulatory requirements applicable to clinical research. Awareness of research ethics. Above average oral, written and communication skills. Independent judgement is employed in problem solving for project management with supervision. Must be highly responsible and capable of seeing each project to its conclusion Please note there will be Frequent travel throughout the UK , with occasional trips to sites across Europe. Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Jun 23, 2018
OrionGroup are looking for a Clinical Research Monitor for our multinational lifesciences client based in the West Yorkshire area on an initial 12-month contract. Please note there will be frequent travel throughout the UK and occasional travel to sites across Europe. SUMMARY OF POSITION: Provide support to the implementation of the clinical research operations programme for all appropriate therapeutic areas for the company in accordance with all applicable regulations for Medical Devices. Plan & implement a programme of monitoring for all international regulatory and post marketing clinical research studies and maintain the highest ethical, clinical and scientific standards ensuring both the safety and well being of all trial participants, and good/rigorous scientific practice. Main Responsibilities of the role Provide support to EMEA Monitoring Resource Manager and act as the lead monitor within the EMEA region. Provide feedback on current and best monitoring practice, procedural and regulatory compliance, and system adoption (e.g. electronic TMF and Clinical Trial Management System (CTMS)). Perform monitor observation visits throughout the EMEA region and provide feedback to EMEA Monitoring Resource Manager. Provide support to Clinical Trial Leader for agreed projects in the EMEA Clinical Research programme for the defined therapeutic area by monitoring and reporting on studies progress in accordance with all Corporate and Statutory requirements to agreed timescales. Maintain the highest ethical, clinical and scientific standards ensuring both the safety and well being of all trial participants and good/rigorous scientific practice. Keep abreast of international legislation and other requirements concerning clinical research. Prepare and submit submissions for the approval of clinical investigations to regulatory authorities and ethics committees. Keep abreast of developments in clinical research and the clinical literature in therapeutic areas of responsibility. Assist in the preparation of consent documentation where required for the proper scientific evaluation of new or existing products in accordance with all ethical and regulatory requirements for Medical Devices in respect of applicable European and International Medical Devices Regulations. Monitor defined clinical studies in accordance with Good Clinical Practice requirements and provide regular feedback to company personnel on the progress of trials. Administer the inventory of Investigational Products and control the issue of investigational products to approved sites where necessary. Participate in project teams and build relationships with investigators, regulatory bodies and appropriate company personnel as required regarding clinical research issues, working as directed by Clinical Trial Leader & monitoring team. Maintain compliance with Company SOPs. Maintain a high standard of housekeeping and filing accuracy. Ideal Background and Skillset of the successful candidate 1st Degree in Life Sciences, Health Sciences or related field to Biomedical Engineering or equivalent combination of education and experience. 5+ years' experience of clinical trials monitoring in a medical company preferably with medical devices. Knowledge of clinical study design and management. Relevant experience in implementation of clinical research studies. Working knowledge of international regulatory requirements applicable to clinical research. Awareness of research ethics. Above average oral, written and communication skills. Independent judgement is employed in problem solving for project management with supervision. Must be highly responsible and capable of seeing each project to its conclusion Please note there will be Frequent travel throughout the UK , with occasional trips to sites across Europe. Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Tbi Outsourcing Uk Ltd
Harrogate, North Yorkshire, UK
Covance, a leading global drug development services company, is looking for Research Analysts to join the Immunochemistry team based in Harrogate, North Yorkshire . Job Description: Research Analyst has a responsibility to work with Study Directors (SDs) and Responsible..... click apply for full job details
Jun 23, 2018
Full time
Covance, a leading global drug development services company, is looking for Research Analysts to join the Immunochemistry team based in Harrogate, North Yorkshire . Job Description: Research Analyst has a responsibility to work with Study Directors (SDs) and Responsible..... click apply for full job details
Carrington West Limited
255 Beeston Rd, Leeds, West Yorkshire LS11 7LR, UK
CAD Technician- Highways I am currently recruiting for a CAD Technician- Highways to join a client based in West Yorkshire. The CAD Technician- Highways will be involved in the delivery of highway works schemes, drawings and electronic designs to the required technical standards and within the required timescale and budget..... click apply for full job details
Jun 23, 2018
Contractor
CAD Technician- Highways I am currently recruiting for a CAD Technician- Highways to join a client based in West Yorkshire. The CAD Technician- Highways will be involved in the delivery of highway works schemes, drawings and electronic designs to the required technical standards and within the required timescale and budget..... click apply for full job details
ProPharma Group
Birmingham, Birmingham, West Midlands, UK
Job Description Multilingual Medical Information Officer - French Olliver Rd, Richmond DL10 5QA, UK Full-time Company Description ProPharma Group is an industry leading provider for medical information services. This is an exciting opportunity in a successful, expanding business based in Richmond, North Yorkshire; however we will also consider candidates who wish to work remotely from their home location in the United Kingdom. We're looking for candidates who have French as their mother tongue, with a keen interest in science, (and a life science degree), with a high level of attention to detail and a customer-focused approach. If you are a strong communicator, who is keen to learn and develop in a rapidly growing organisation, we are keen to work with you to develop your strengths and provide career opportunities within ProPharma Group. Job Description You must be confident, proactive and passionate about delivering great customer service. Experience in customer facing roles is desirable but not essential, and new graduates are welcome to apply. We will provide excellent training to help you learn our processes and plenty of opportunities to expand your skills and experience. Every day will provide both challenge and variety and you will work in a friendly, hard-working team supporting colleagues in the UK, USA, EU, Australia and Japan. You will be flexible, with a willingness to take on additional responsibilities and, in return, we will provide opportunities for you to continually learn and develop while participating in new and exciting projects. Comprehensive on boarding training is provided to support you. A "buddy" will be allocated to you to support you in the following essential functions of the role: 1. Providing a high quality medical information enquiry handling service by answering technical questions in respect of designated products in an accurate, confident and professional manner. Enquiries may be received via phone, letter, email and fax. 2. Complying with the specific Working Practices (WPs) which have been agreed with designated clients as well as following processes which may be documented in Client Instructions/other documentation. 3. Ensuring that tasks are completed within the deadlines documented in the agreed ProPharma Group SOPs and WPs. 4. Recognising adverse events and defective product reports and handling and reporting these in strict compliance with agreed ProPharma Group SOPs and WPs. 5. Translating English documents into the target language or vice versa, and delivering these translated responses either on the phone or in writing. 6. Using existing standard responses to prepare medical information correspondence (via client databases) or taking responsibility for liaising with the Medical Information Support Services (MISS) department to request the generation of medical information correspondence. 7. Logging all enquiries handled in an accurate, comprehensive and timely fashion in to Enquiry Handling Systems. Qualifications Qualifications: A degree in a life science or pharmacy e.g. BSc Biomedical Sciences, BSc Anatomy & Physiology, BSc Health Science, BSc Human Science, BSc Psychology, BSc Animal Science We welcome applications from all life science graduates. Key skills: 1. Candidates should have the target language as their mother tongue, be fluent in English and have strong translation skills. 2. Able to work within a team in an open and professional manner. 3. Excellent written and oral communication skills and computer literacy. 4. Sound planning, prioritising and organisational skills, effective workload management and ability to meet deadlines. 5. Able to take responsibility for work allocated (ensuring tasks are followed through to completion). 6. Accuracy and attention to detail. Additional Information All candidates must be legally eligible to work in the United Kingdom. We are an equal opportunity employer. M/F/D/V ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
Jun 23, 2018
Full time
Job Description Multilingual Medical Information Officer - French Olliver Rd, Richmond DL10 5QA, UK Full-time Company Description ProPharma Group is an industry leading provider for medical information services. This is an exciting opportunity in a successful, expanding business based in Richmond, North Yorkshire; however we will also consider candidates who wish to work remotely from their home location in the United Kingdom. We're looking for candidates who have French as their mother tongue, with a keen interest in science, (and a life science degree), with a high level of attention to detail and a customer-focused approach. If you are a strong communicator, who is keen to learn and develop in a rapidly growing organisation, we are keen to work with you to develop your strengths and provide career opportunities within ProPharma Group. Job Description You must be confident, proactive and passionate about delivering great customer service. Experience in customer facing roles is desirable but not essential, and new graduates are welcome to apply. We will provide excellent training to help you learn our processes and plenty of opportunities to expand your skills and experience. Every day will provide both challenge and variety and you will work in a friendly, hard-working team supporting colleagues in the UK, USA, EU, Australia and Japan. You will be flexible, with a willingness to take on additional responsibilities and, in return, we will provide opportunities for you to continually learn and develop while participating in new and exciting projects. Comprehensive on boarding training is provided to support you. A "buddy" will be allocated to you to support you in the following essential functions of the role: 1. Providing a high quality medical information enquiry handling service by answering technical questions in respect of designated products in an accurate, confident and professional manner. Enquiries may be received via phone, letter, email and fax. 2. Complying with the specific Working Practices (WPs) which have been agreed with designated clients as well as following processes which may be documented in Client Instructions/other documentation. 3. Ensuring that tasks are completed within the deadlines documented in the agreed ProPharma Group SOPs and WPs. 4. Recognising adverse events and defective product reports and handling and reporting these in strict compliance with agreed ProPharma Group SOPs and WPs. 5. Translating English documents into the target language or vice versa, and delivering these translated responses either on the phone or in writing. 6. Using existing standard responses to prepare medical information correspondence (via client databases) or taking responsibility for liaising with the Medical Information Support Services (MISS) department to request the generation of medical information correspondence. 7. Logging all enquiries handled in an accurate, comprehensive and timely fashion in to Enquiry Handling Systems. Qualifications Qualifications: A degree in a life science or pharmacy e.g. BSc Biomedical Sciences, BSc Anatomy & Physiology, BSc Health Science, BSc Human Science, BSc Psychology, BSc Animal Science We welcome applications from all life science graduates. Key skills: 1. Candidates should have the target language as their mother tongue, be fluent in English and have strong translation skills. 2. Able to work within a team in an open and professional manner. 3. Excellent written and oral communication skills and computer literacy. 4. Sound planning, prioritising and organisational skills, effective workload management and ability to meet deadlines. 5. Able to take responsibility for work allocated (ensuring tasks are followed through to completion). 6. Accuracy and attention to detail. Additional Information All candidates must be legally eligible to work in the United Kingdom. We are an equal opportunity employer. M/F/D/V ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
OrionGroup is looking for a Microbiology Technician for our multinational medical devices client based in the Lancashire area on an initial 6-month contract. Summary of position To carry out microbiological testing to ensure the ongoing quality of product. -To interface with other Departments to ensure the timely approval of products. -Support investigation of laboratory (OOS) and manufacturing issues (OOS/non-conformances) -To ensure that the principles of cGMP are applied and that all documentation, in the form of procedures and specifications, is followed to guarantee compliance with ISO 9000, ISO 13485, FDA QSRs and the Medical Devices Directive. Main Responsibilities of the role: Ensure that all routine microbiological testing is performed in a timely manner in line with agreed schedules Day to Day performance - Bioburden testing of raw and in process materials - Sterility testing of final products - Gentamicin assay - Environmental monitoring. - Enumeration and identification of microbiological contaminants. - Management of consumables and materials used in testing. To ensure that the principles of cGMP are applied and that all documentation, in the form of procedures and specifications, are followed correctly. Ability to communicate & present (in all its forms) an co-operate effectively at all levels across the organization. Ability to manage their own time and workload and to work independently using own initiative (Excellent time-management) GMP documentation and Quality Systems Ideal background and Experience of the successful candidate Minimum of Degree level in a relevant Biological scientific discipline or equivalent. Minimum 1-3 years' experience within a Microbiological role in the Food, Medical or Health Care industry. Must have experience working in a production laboratory environment Good interpersonal and communication skills. Basic familiarity with a variety of relevant technologies and test methods. Demonstrable basic technical skills acquired in a relevant scientific role. Basic knowledge of cGMP and documentation practise Good numerical skills and Computer literacy Good understanding of Bioburden and environmental monitoring requirement An attention to detail Ability to work to deadlines Ability to cope under pressure and to react to changing requirements Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Jun 23, 2018
OrionGroup is looking for a Microbiology Technician for our multinational medical devices client based in the Lancashire area on an initial 6-month contract. Summary of position To carry out microbiological testing to ensure the ongoing quality of product. -To interface with other Departments to ensure the timely approval of products. -Support investigation of laboratory (OOS) and manufacturing issues (OOS/non-conformances) -To ensure that the principles of cGMP are applied and that all documentation, in the form of procedures and specifications, is followed to guarantee compliance with ISO 9000, ISO 13485, FDA QSRs and the Medical Devices Directive. Main Responsibilities of the role: Ensure that all routine microbiological testing is performed in a timely manner in line with agreed schedules Day to Day performance - Bioburden testing of raw and in process materials - Sterility testing of final products - Gentamicin assay - Environmental monitoring. - Enumeration and identification of microbiological contaminants. - Management of consumables and materials used in testing. To ensure that the principles of cGMP are applied and that all documentation, in the form of procedures and specifications, are followed correctly. Ability to communicate & present (in all its forms) an co-operate effectively at all levels across the organization. Ability to manage their own time and workload and to work independently using own initiative (Excellent time-management) GMP documentation and Quality Systems Ideal background and Experience of the successful candidate Minimum of Degree level in a relevant Biological scientific discipline or equivalent. Minimum 1-3 years' experience within a Microbiological role in the Food, Medical or Health Care industry. Must have experience working in a production laboratory environment Good interpersonal and communication skills. Basic familiarity with a variety of relevant technologies and test methods. Demonstrable basic technical skills acquired in a relevant scientific role. Basic knowledge of cGMP and documentation practise Good numerical skills and Computer literacy Good understanding of Bioburden and environmental monitoring requirement An attention to detail Ability to work to deadlines Ability to cope under pressure and to react to changing requirements Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
An opportunity for a graduate in a chemistry related subject who speaks fluent Spanish and who is interested in starting their career in regulatory affairs. You will join the regulatory department of a successful and expanding global chemicals business and be trained in all aspects of regulatory affairs so that you can provide regulatory support to the Spanish division. The role can be based in Cheshire or Valencia - you will initially be trained in the EU had office in Cheshire - you can then remain in the Cheshire Head Office or relocate to Spain. Suitable candidates will be recent chemistry graduates and you must speak fluent Spanish. You may be a Spanish student studying in the UK, or a British student with exception Spanish language skills. You must also have excellent attention to detail and be looking for a desk based scientific/chemistry related role. You must be able to learn quickly and be ready to be trained in regulatory affairs so that you can provide high quality regulatory support for the fast expanding Spanish division. For an immediate confidential discussion, please contact John Sherratt at VRS Regulatory Key Skills: Fluent Spanish is essential, chemistry, science, Regulatory Affairs, regulatory compliance, chemical data, analytical data, attention to detail, accuracy, communication skills, strong Excel. VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.
Jun 23, 2018
An opportunity for a graduate in a chemistry related subject who speaks fluent Spanish and who is interested in starting their career in regulatory affairs. You will join the regulatory department of a successful and expanding global chemicals business and be trained in all aspects of regulatory affairs so that you can provide regulatory support to the Spanish division. The role can be based in Cheshire or Valencia - you will initially be trained in the EU had office in Cheshire - you can then remain in the Cheshire Head Office or relocate to Spain. Suitable candidates will be recent chemistry graduates and you must speak fluent Spanish. You may be a Spanish student studying in the UK, or a British student with exception Spanish language skills. You must also have excellent attention to detail and be looking for a desk based scientific/chemistry related role. You must be able to learn quickly and be ready to be trained in regulatory affairs so that you can provide high quality regulatory support for the fast expanding Spanish division. For an immediate confidential discussion, please contact John Sherratt at VRS Regulatory Key Skills: Fluent Spanish is essential, chemistry, science, Regulatory Affairs, regulatory compliance, chemical data, analytical data, attention to detail, accuracy, communication skills, strong Excel. VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.
Account Manager - Life Sciences A great opportunity has arisen for an Account Manager to an international Biotechnology company manufacturing reagents for use in Life Science research laboratories. Coming about through rapid growth, this is an opportunity for an Account Manager to be based in their Manchester office with the responsibility for customers in Academic and Industrial institutions. The role will be based primarily in the office but with occasional travel for exhibitions and customer visits. This role offers real responsibility and exposure to multiple facets of the business, with potential for rapid career development for the right candidate. On offer is a competitive salary (negotiable dependent on experience), pension and generous bonus scheme. Responsibilities • Maintain and develop relationships with existing customers with a view to growing long-term and effective business relationships. • Pro-actively search and connect with new prospects. A key part of this role will be business development and new customer generation. • Utilize interpersonal and communication skills to provide effective solutions to customer needs, with technical support provided from in house team. • Attend seminars and exhibitions to further build brand awareness. • Provide feedback to Marketing and Product development on customer and competitor activities. • Responsible for meeting and reporting on sales targets (revenue & KPI). Essentials • Interest in developing a career in Sales & Marketing in Biotechnology. • Life Sciences qualification (or equivalent) • Preferably lab experience and understanding of antibody techniques (in addition an understanding of Cell Therapy and Regenerative Medicine would be highly beneficial but is not essential). • Fluent German Speaker favourable • Professional communication skills • Independent, driven and able to work on own initiative. • Strong time management and organizational skills If this sounds like opportunity for you, apply now with your CV. Feel free to contact Tom Kirkpatrick at CY Partners for more information.
Jun 23, 2018
Account Manager - Life Sciences A great opportunity has arisen for an Account Manager to an international Biotechnology company manufacturing reagents for use in Life Science research laboratories. Coming about through rapid growth, this is an opportunity for an Account Manager to be based in their Manchester office with the responsibility for customers in Academic and Industrial institutions. The role will be based primarily in the office but with occasional travel for exhibitions and customer visits. This role offers real responsibility and exposure to multiple facets of the business, with potential for rapid career development for the right candidate. On offer is a competitive salary (negotiable dependent on experience), pension and generous bonus scheme. Responsibilities • Maintain and develop relationships with existing customers with a view to growing long-term and effective business relationships. • Pro-actively search and connect with new prospects. A key part of this role will be business development and new customer generation. • Utilize interpersonal and communication skills to provide effective solutions to customer needs, with technical support provided from in house team. • Attend seminars and exhibitions to further build brand awareness. • Provide feedback to Marketing and Product development on customer and competitor activities. • Responsible for meeting and reporting on sales targets (revenue & KPI). Essentials • Interest in developing a career in Sales & Marketing in Biotechnology. • Life Sciences qualification (or equivalent) • Preferably lab experience and understanding of antibody techniques (in addition an understanding of Cell Therapy and Regenerative Medicine would be highly beneficial but is not essential). • Fluent German Speaker favourable • Professional communication skills • Independent, driven and able to work on own initiative. • Strong time management and organizational skills If this sounds like opportunity for you, apply now with your CV. Feel free to contact Tom Kirkpatrick at CY Partners for more information.
An opportunity for a chemical sector regulatory affairs officer to join an expanding and highly innovative consumer products company. You will be trained to take responsibility for the regulatory affairs and notifications or their products across the EU. They develop and sell a range of natural substances An opportunity to join a specialist active substance manufacturer as the EU Regulatory Affairs Manager. The company owns and supplies a naturally derived active substance used in biocidal products globally. You will support the global regulatory director by managing EU product registrations and providing regulatory support to a diverse range of customers. Duties will be diverse, interesting and challenging; you will prepare regulatory submissions and renewals, review in-house and externally generated studies, liaise with regulatory authorities and maintain/further develop a working knowledge of the relevant regulations including the BPR. You will also manage and work with external technical experts to assist in regulatory submissions. The company has a diverse range of customers many of whom will require regulatory support for their product dossier submissions and registrations. Support will be tailored to individual customer needs. You will input regulatory expertise to product labelling, SDSs and CoAs, provide support to marketing materials and monitor relevant ECHA guidance immediately relevant to the product set and active substances. In addition to the EU registration work, you will assist in obtaining and improving global active substance registrations. We are looking for a regulatory affairs officer / specialist or manager who is interested in playing a key role in managing a EU biocidal product set. Ideally you will have existing BPR knowledge and experience of national registration or AS support, but we are also interested in people from a PPP or REACH background who would like to diversify. You must have a meticulous approach, strong attention to detail, be self-starting, be adaptable and have confident communications skills enabling you to be credible with customers. AN excellent opportunity. For an immediate confidential discussion, please contact John Sherratt at VRS Regulatory Key Skills: Regulatory Affairs, regulatory compliance, biocides, product registrations, regulatory support, labels, SDSs, BPR, REACH, PPP, data, attention to detail, accuracy, communication skills. VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.
Jun 23, 2018
An opportunity for a chemical sector regulatory affairs officer to join an expanding and highly innovative consumer products company. You will be trained to take responsibility for the regulatory affairs and notifications or their products across the EU. They develop and sell a range of natural substances An opportunity to join a specialist active substance manufacturer as the EU Regulatory Affairs Manager. The company owns and supplies a naturally derived active substance used in biocidal products globally. You will support the global regulatory director by managing EU product registrations and providing regulatory support to a diverse range of customers. Duties will be diverse, interesting and challenging; you will prepare regulatory submissions and renewals, review in-house and externally generated studies, liaise with regulatory authorities and maintain/further develop a working knowledge of the relevant regulations including the BPR. You will also manage and work with external technical experts to assist in regulatory submissions. The company has a diverse range of customers many of whom will require regulatory support for their product dossier submissions and registrations. Support will be tailored to individual customer needs. You will input regulatory expertise to product labelling, SDSs and CoAs, provide support to marketing materials and monitor relevant ECHA guidance immediately relevant to the product set and active substances. In addition to the EU registration work, you will assist in obtaining and improving global active substance registrations. We are looking for a regulatory affairs officer / specialist or manager who is interested in playing a key role in managing a EU biocidal product set. Ideally you will have existing BPR knowledge and experience of national registration or AS support, but we are also interested in people from a PPP or REACH background who would like to diversify. You must have a meticulous approach, strong attention to detail, be self-starting, be adaptable and have confident communications skills enabling you to be credible with customers. AN excellent opportunity. For an immediate confidential discussion, please contact John Sherratt at VRS Regulatory Key Skills: Regulatory Affairs, regulatory compliance, biocides, product registrations, regulatory support, labels, SDSs, BPR, REACH, PPP, data, attention to detail, accuracy, communication skills. VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.
ProPharma Group
16 Hestham Cres, Morecambe, Morecambe, Lancashire LA4 4QF, UK
Job Description Multilingual Medical Information Officer - French Remote Working (Home based) Full-time Company Description ProPharma Group is an industry leading provider for medical information services. This is an exciting opportunity in a successful, expanding business based in Richmond, North Yorkshire; however we will also consider candidates who wish to work remotely from their home location in the United Kingdom. We're looking for candidates who have French as their mother tongue, with a keen interest in science, (and a life science degree), with a high level of attention to detail and a customer-focused approach. If you are a strong communicator, who is keen to learn and develop in a rapidly growing organisation, we are keen to work with you to develop your strengths and provide career opportunities within ProPharma Group. Job Description You must be confident, proactive and passionate about delivering great customer service. Experience in customer facing roles is desirable but not essential, and new graduates are welcome to apply. We will provide excellent training to help you learn our processes and plenty of opportunities to expand your skills and experience. Every day will provide both challenge and variety and you will work in a friendly, hard-working team supporting colleagues in the UK, USA, EU, Australia and Japan. You will be flexible, with a willingness to take on additional responsibilities and, in return, we will provide opportunities for you to continually learn and develop while participating in new and exciting projects. Comprehensive on boarding training is provided to support you. A "buddy" will be allocated to you to support you in the following essential functions of the role: 1. Providing a high quality medical information enquiry handling service by answering technical questions in respect of designated products in an accurate, confident and professional manner. Enquiries may be received via phone, letter, email and fax. 2. Complying with the specific Working Practices (WPs) which have been agreed with designated clients as well as following processes which may be documented in Client Instructions/other documentation. 3. Ensuring that tasks are completed within the deadlines documented in the agreed ProPharma Group SOPs and WPs. 4. Recognising adverse events and defective product reports and handling and reporting these in strict compliance with agreed ProPharma Group SOPs and WPs. 5. Translating English documents into the target language or vice versa, and delivering these translated responses either on the phone or in writing. 6. Using existing standard responses to prepare medical information correspondence (via client databases) or taking responsibility for liaising with the Medical Information Support Services (MISS) department to request the generation of medical information correspondence. 7. Logging all enquiries handled in an accurate, comprehensive and timely fashion in to Enquiry Handling Systems. Qualifications Qualifications: A degree in a life science or pharmacy e.g. BSc Biomedical Sciences, BSc Anatomy & Physiology, BSc Health Science, BSc Human Science, BSc Psychology, BSc Animal Science We welcome applications from all life science graduates. Key skills: 1. Candidates should have the target language as their mother tongue, be fluent in English and have strong translation skills. 2. Able to work within a team in an open and professional manner. 3. Excellent written and oral communication skills and computer literacy. 4. Sound planning, prioritising and organisational skills, effective workload management and ability to meet deadlines. 5. Able to take responsibility for work allocated (ensuring tasks are followed through to completion). 6. Accuracy and attention to detail. Additional Information All candidates must be legally eligible to work in the United Kingdom. We are an equal opportunity employer. M/F/D/V ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
Jun 23, 2018
Full time
Job Description Multilingual Medical Information Officer - French Remote Working (Home based) Full-time Company Description ProPharma Group is an industry leading provider for medical information services. This is an exciting opportunity in a successful, expanding business based in Richmond, North Yorkshire; however we will also consider candidates who wish to work remotely from their home location in the United Kingdom. We're looking for candidates who have French as their mother tongue, with a keen interest in science, (and a life science degree), with a high level of attention to detail and a customer-focused approach. If you are a strong communicator, who is keen to learn and develop in a rapidly growing organisation, we are keen to work with you to develop your strengths and provide career opportunities within ProPharma Group. Job Description You must be confident, proactive and passionate about delivering great customer service. Experience in customer facing roles is desirable but not essential, and new graduates are welcome to apply. We will provide excellent training to help you learn our processes and plenty of opportunities to expand your skills and experience. Every day will provide both challenge and variety and you will work in a friendly, hard-working team supporting colleagues in the UK, USA, EU, Australia and Japan. You will be flexible, with a willingness to take on additional responsibilities and, in return, we will provide opportunities for you to continually learn and develop while participating in new and exciting projects. Comprehensive on boarding training is provided to support you. A "buddy" will be allocated to you to support you in the following essential functions of the role: 1. Providing a high quality medical information enquiry handling service by answering technical questions in respect of designated products in an accurate, confident and professional manner. Enquiries may be received via phone, letter, email and fax. 2. Complying with the specific Working Practices (WPs) which have been agreed with designated clients as well as following processes which may be documented in Client Instructions/other documentation. 3. Ensuring that tasks are completed within the deadlines documented in the agreed ProPharma Group SOPs and WPs. 4. Recognising adverse events and defective product reports and handling and reporting these in strict compliance with agreed ProPharma Group SOPs and WPs. 5. Translating English documents into the target language or vice versa, and delivering these translated responses either on the phone or in writing. 6. Using existing standard responses to prepare medical information correspondence (via client databases) or taking responsibility for liaising with the Medical Information Support Services (MISS) department to request the generation of medical information correspondence. 7. Logging all enquiries handled in an accurate, comprehensive and timely fashion in to Enquiry Handling Systems. Qualifications Qualifications: A degree in a life science or pharmacy e.g. BSc Biomedical Sciences, BSc Anatomy & Physiology, BSc Health Science, BSc Human Science, BSc Psychology, BSc Animal Science We welcome applications from all life science graduates. Key skills: 1. Candidates should have the target language as their mother tongue, be fluent in English and have strong translation skills. 2. Able to work within a team in an open and professional manner. 3. Excellent written and oral communication skills and computer literacy. 4. Sound planning, prioritising and organisational skills, effective workload management and ability to meet deadlines. 5. Able to take responsibility for work allocated (ensuring tasks are followed through to completion). 6. Accuracy and attention to detail. Additional Information All candidates must be legally eligible to work in the United Kingdom. We are an equal opportunity employer. M/F/D/V ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Company Description ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the United States, United Kingdom, Australia, and Japan, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
Exciting opportunity to join an internationally renowned research laboratory in a unique new role! Are you a budding scientist looking for a new challenge outside of the lab? Do you want to take a step in the direction of project management? Are you an organised and analytical thinking individual? In this pivotal role you will work closely alongside Study Directors/Project Managers to: Establish and amend laboratory study plans in collaboration with external sponsors Keep study schedules updated throughout the study process Ensure study documents are compliant with regulatory requirements (GLP, GMP) and SOP's and respond to QA audit findings Assist in the preparation of study reports Manage and archive study documentation Successful applicants must have: Minimum 12 months experience within a regulated analytical laboratory Document editing experience Great attention to detail Experience within GMP, GLP, or GCP accreditation is helpful Excellent time keeping Superb communication skills Applications are invited from enthusiastic and motivated individuals who are looking for a progression away from the lab! Apply to VRS now for this exciting opportunity! Key Words: Analytical Chemist, Pharmaceutical, Biopharmaceutical, Analyst, GC, Study Support, Administrative, Project Management, GMP, GLP, GCP, HPLC, Chromatography, Mass Spectrometry, Mass Spec, Manchester, Greater Manchester, North West, VRS5934LW
Jun 23, 2018
Exciting opportunity to join an internationally renowned research laboratory in a unique new role! Are you a budding scientist looking for a new challenge outside of the lab? Do you want to take a step in the direction of project management? Are you an organised and analytical thinking individual? In this pivotal role you will work closely alongside Study Directors/Project Managers to: Establish and amend laboratory study plans in collaboration with external sponsors Keep study schedules updated throughout the study process Ensure study documents are compliant with regulatory requirements (GLP, GMP) and SOP's and respond to QA audit findings Assist in the preparation of study reports Manage and archive study documentation Successful applicants must have: Minimum 12 months experience within a regulated analytical laboratory Document editing experience Great attention to detail Experience within GMP, GLP, or GCP accreditation is helpful Excellent time keeping Superb communication skills Applications are invited from enthusiastic and motivated individuals who are looking for a progression away from the lab! Apply to VRS now for this exciting opportunity! Key Words: Analytical Chemist, Pharmaceutical, Biopharmaceutical, Analyst, GC, Study Support, Administrative, Project Management, GMP, GLP, GCP, HPLC, Chromatography, Mass Spectrometry, Mass Spec, Manchester, Greater Manchester, North West, VRS5934LW
