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1,096 Biotech jobs

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Search Consultancy
Laboratory Technician
Search Consultancy 133 Oldham St, Manchester M4 1LN, UK
Do you have an interest in Science? Would you be interested in a career within a laboratory environment? I have a great opportunity for someone with an A-level or equivalent qualification in science. My client has an urgent requirement for a laboratory technician to join there team. Full training will be provided but a good work ethic and a positive attitude is an absolute must. If you are a recent school leaver or have started work in a different field and you would like to explore a role in a fast paced and challenging laboratory environment then please apply now! 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.
Feb 21, 2019
Do you have an interest in Science? Would you be interested in a career within a laboratory environment? I have a great opportunity for someone with an A-level or equivalent qualification in science. My client has an urgent requirement for a laboratory technician to join there team. Full training will be provided but a good work ethic and a positive attitude is an absolute must. If you are a recent school leaver or have started work in a different field and you would like to explore a role in a fast paced and challenging laboratory environment then please apply now! 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.
CK Group
Occupational Hygienist in Speke
CK Group Speke, UK
Lucy Stendall at CK Group is recruiting for an Occupational Hygienist Advisor to join an international statistics team who provide innovative scientific and operational excellence in design, analysis, and interpretation in order to convert scientific information to knowledge that is useful to payers, consumers and patients. This would be based either at our clients office in Speke on a 12 month contract. The Company: Our client is an innovative company where you will have the opportunity to support the work of thousands of others around the globe dedicated to improving the lives of others. They discover and bring life-changing medicines to those who need them, improving the understanding and management of disease and giving back to communities through philanthropy and volunteerism. Their values are integrity, excellence and respect for people. The Location: The role will be based at our clients site in Speke, an area of Liverpool close to the boundaries of the Metropolitan Borough of Knowsley. It is 7.7 miles south east of the city centre making it easily accessible via car and boasts great public transport links. The Role: • To provide specialist advice and leadership to management and workforce by interpreting health & safety legislation, policies and industry guidance; developing management systems and standards and providing training and technical support for occupational hygiene. • To ensure company compliance and continuous improvement in H&S standards by auditing and reviewing the safety management system. Responsibilities include: • To provide expert Occupational Hygiene advice, leadership and technical expertise in the form of written policies, guidelines and procedures, verbal communications and practical involvement both internally, within the corporation and externally. • To participate in the development, progression and implementation of the site safety management system, and to attend Team H&S meetings in order to promote the SMS philosophy and obtain feedback to ensure consistency in standards and approach. • To interpret and ensure appropriate application of all Occupational Hygiene legislation from UK and Europe and incorporate them into Corporate H&S policies and guidelines. Be aware of and prepare for changes in legislation. • Ensure adequate provision of Occupational Hygiene training for company employees and contractors, and specific training and development of EHS Co-ordinators, through external training providers and/or development and delivery of 'in-house' training packages. • Facilitate and sustain risk assessments(CoSHH) and other programmes to meet regulatory and corporate requirements. Be focal point of contact for Regulatory and corporate agencies with respect to Occupational Hygiene issues. • Participate in projects both at the Speke site and for Corporate H&S, and input into developing projects. Where appropriate, review process and equipment change controls to ensure no negative impact on Occupational Hygiene requirements. • Participate in, train and give guidance on team inspections and audits, giving guidance to Corporate audit team. Participate in audits and development of the site audit programme with regard to Occupational Hygiene. • Maintain and update knowledge by attendance at seminars, courses and conferences, and reading of relevant H&S journals and publications. Share best practices across teams on site. Maintain current level of qualification. Your Background: • Certificate of Competence in Occupational Hygiene. • Good communication skills and ability to prioritise. • Able to make decisions that impact own priorities and allocation of time to meet deadlines. • Able to impact within local area. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference KA44499 in all correspondence.
Feb 21, 2019
Lucy Stendall at CK Group is recruiting for an Occupational Hygienist Advisor to join an international statistics team who provide innovative scientific and operational excellence in design, analysis, and interpretation in order to convert scientific information to knowledge that is useful to payers, consumers and patients. This would be based either at our clients office in Speke on a 12 month contract. The Company: Our client is an innovative company where you will have the opportunity to support the work of thousands of others around the globe dedicated to improving the lives of others. They discover and bring life-changing medicines to those who need them, improving the understanding and management of disease and giving back to communities through philanthropy and volunteerism. Their values are integrity, excellence and respect for people. The Location: The role will be based at our clients site in Speke, an area of Liverpool close to the boundaries of the Metropolitan Borough of Knowsley. It is 7.7 miles south east of the city centre making it easily accessible via car and boasts great public transport links. The Role: • To provide specialist advice and leadership to management and workforce by interpreting health & safety legislation, policies and industry guidance; developing management systems and standards and providing training and technical support for occupational hygiene. • To ensure company compliance and continuous improvement in H&S standards by auditing and reviewing the safety management system. Responsibilities include: • To provide expert Occupational Hygiene advice, leadership and technical expertise in the form of written policies, guidelines and procedures, verbal communications and practical involvement both internally, within the corporation and externally. • To participate in the development, progression and implementation of the site safety management system, and to attend Team H&S meetings in order to promote the SMS philosophy and obtain feedback to ensure consistency in standards and approach. • To interpret and ensure appropriate application of all Occupational Hygiene legislation from UK and Europe and incorporate them into Corporate H&S policies and guidelines. Be aware of and prepare for changes in legislation. • Ensure adequate provision of Occupational Hygiene training for company employees and contractors, and specific training and development of EHS Co-ordinators, through external training providers and/or development and delivery of 'in-house' training packages. • Facilitate and sustain risk assessments(CoSHH) and other programmes to meet regulatory and corporate requirements. Be focal point of contact for Regulatory and corporate agencies with respect to Occupational Hygiene issues. • Participate in projects both at the Speke site and for Corporate H&S, and input into developing projects. Where appropriate, review process and equipment change controls to ensure no negative impact on Occupational Hygiene requirements. • Participate in, train and give guidance on team inspections and audits, giving guidance to Corporate audit team. Participate in audits and development of the site audit programme with regard to Occupational Hygiene. • Maintain and update knowledge by attendance at seminars, courses and conferences, and reading of relevant H&S journals and publications. Share best practices across teams on site. Maintain current level of qualification. Your Background: • Certificate of Competence in Occupational Hygiene. • Good communication skills and ability to prioritise. • Able to make decisions that impact own priorities and allocation of time to meet deadlines. • Able to impact within local area. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference KA44499 in all correspondence.
Graduate QC Pharmaceutical Analyst
Russell Taylor Associates Skipton BD23, UK
Position: QC Analyst Location: Skipton, North Yorkshire Type: Permanent Salary: Competitive My client is a successful contract research organisation undergoing rapid expansion, & are looking for a talented pharmaceutical QC Analyst to join their team. Job description: * Working to strict GMP & GLP * Using both hard-copy & electronic data capture systems within QMS guidelines * Working to good manufacturing practice * Ensuring cleanliness of laboratories & individual workplace * Performing analytical techniques (EG HPLC & LCMS) * Working with the analytical team during product development/registration/optimisation/validation/launch of pharmaceutical products. * Implementing effective chromatographic methods. * Performing investigations into out of specification results. * Coordinating between departments to ensure timely performance of projects. * Inventory checks of chemicals, consumer goods & equipment Candidate Requirements: * Minimum of BSc in a relevant pharmaceutical, scientific, life science, or chemical field Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h u s s e l l - t a y l o r . c o . u k
Feb 21, 2019
Position: QC Analyst Location: Skipton, North Yorkshire Type: Permanent Salary: Competitive My client is a successful contract research organisation undergoing rapid expansion, & are looking for a talented pharmaceutical QC Analyst to join their team. Job description: * Working to strict GMP & GLP * Using both hard-copy & electronic data capture systems within QMS guidelines * Working to good manufacturing practice * Ensuring cleanliness of laboratories & individual workplace * Performing analytical techniques (EG HPLC & LCMS) * Working with the analytical team during product development/registration/optimisation/validation/launch of pharmaceutical products. * Implementing effective chromatographic methods. * Performing investigations into out of specification results. * Coordinating between departments to ensure timely performance of projects. * Inventory checks of chemicals, consumer goods & equipment Candidate Requirements: * Minimum of BSc in a relevant pharmaceutical, scientific, life science, or chemical field Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h u s s e l l - t a y l o r . c o . u k
North Yorkshire County Council
Waste Management Opportunities
North Yorkshire County Council 41, Barkston House, Croydon St, Leeds LS11 9RT, UK
Waste Management Opportunities Location: Northallerton, North Yorkshire Salary: Ranging from £42,683 to £66,000, subject to pay award agreement and dependent upon experience Are you a strategic waste management professional? Could you take us to the next part of our journey from waste to resources management? Our waste Management service has a number of exciting opportunities for strategic waste management professionals. The Waste Management Service forms part of the Business and Environmental Services Directorate, which is situated at County Hall, Northallerton. This is a really unique time for our service, having worked closely with the City of York Council, we have secured a long term waste treatment facility within the County and want to ensure we maximise the potential of the plant for the benefit of both councils. We have a strong history of working in partnership with City of York, with plans for the services to combine under a single joint service in the near future. Our treatment plant, Allerton waste recovery park (AWRP) is the first site in the UK to bring together three different waste technologies anaerobic digestion, energy from waste and mechanical treatment on one site - allowing us to make the most of all our waste, increasing our recycling and creating renewable energy. AWRP means we are no longer reliant on landfill and have strong resilience to deal with future uncertainties, but we are ambitious to do more. We are committed to working in partnership with the district and borough councils, and our private sector partners to improve services further, to drive out more efficiency and ensure the benefit for the local taxpayer. This is what we do best and this is who we are. Critical to continuing with our ambition is where you come in. As this is a start to a new way of working, we are looking for an ambitious head of service (waste) and an operations manager (waste) to respond to new challenges and develop the service. The roles are about being innovative and continually finding opportunities to improve, working closely with the council's own waste company, Yorwaste, who run all transfer stations and HWRCs, and spotting change and being ahead of the game in responding to it as well as ensuring value for money. If you can deliver benefit realisation and take us on the next phase of our journey then we want to hear from you! Please visit our dedicated campaign site for more information and how to apply, please click the apply button. Closing date: Sunday 17th March 2019 Interview date: Details are included on the campaign site
Feb 21, 2019
Full time
Waste Management Opportunities Location: Northallerton, North Yorkshire Salary: Ranging from £42,683 to £66,000, subject to pay award agreement and dependent upon experience Are you a strategic waste management professional? Could you take us to the next part of our journey from waste to resources management? Our waste Management service has a number of exciting opportunities for strategic waste management professionals. The Waste Management Service forms part of the Business and Environmental Services Directorate, which is situated at County Hall, Northallerton. This is a really unique time for our service, having worked closely with the City of York Council, we have secured a long term waste treatment facility within the County and want to ensure we maximise the potential of the plant for the benefit of both councils. We have a strong history of working in partnership with City of York, with plans for the services to combine under a single joint service in the near future. Our treatment plant, Allerton waste recovery park (AWRP) is the first site in the UK to bring together three different waste technologies anaerobic digestion, energy from waste and mechanical treatment on one site - allowing us to make the most of all our waste, increasing our recycling and creating renewable energy. AWRP means we are no longer reliant on landfill and have strong resilience to deal with future uncertainties, but we are ambitious to do more. We are committed to working in partnership with the district and borough councils, and our private sector partners to improve services further, to drive out more efficiency and ensure the benefit for the local taxpayer. This is what we do best and this is who we are. Critical to continuing with our ambition is where you come in. As this is a start to a new way of working, we are looking for an ambitious head of service (waste) and an operations manager (waste) to respond to new challenges and develop the service. The roles are about being innovative and continually finding opportunities to improve, working closely with the council's own waste company, Yorwaste, who run all transfer stations and HWRCs, and spotting change and being ahead of the game in responding to it as well as ensuring value for money. If you can deliver benefit realisation and take us on the next phase of our journey then we want to hear from you! Please visit our dedicated campaign site for more information and how to apply, please click the apply button. Closing date: Sunday 17th March 2019 Interview date: Details are included on the campaign site
Network Scientific Ltd.
Training Manager
Network Scientific Ltd. 133 Oldham St, Manchester M4 1LN, UK
As Training Manager, you will have full responsibility for creating and implementing a strategy that enables the teams around you to constantly develop themselves through structured training sessions via a combination of internal and external sources. From an initial induction for all new staff members, to dedicated, personalised plans for each member, you will be able to watch technically gifted scientists and commercially astute professionals go from strength to strength under your tutelage. To begin with all structured training will be held in-house, but over time you will source external training providers, some of it online, and factor this into the individuals training requirements. The training itself with cover multiple areas, some with regard to personal improvements such as time management, others will be equipment-specific. Therefore, the need to have at least a fundamental understanding of scientific testing techniques, with knowledge or GMP or GLP being essential for the role. As a result, you are likely to have operated in a laboratory environment already. Diary management and organisation skills are also essential as you will be holding regular, structured reviews with team members and assessing further needs based upon the results. This is a fantastic opportunity to become an integral part of improving an already successful business from within. For more information or to apply, please contact Steve Coomber at Network Scientific. Please note that all applicants for this role should be able to prove that they are legally entitled to work in the UK. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.
Feb 21, 2019
As Training Manager, you will have full responsibility for creating and implementing a strategy that enables the teams around you to constantly develop themselves through structured training sessions via a combination of internal and external sources. From an initial induction for all new staff members, to dedicated, personalised plans for each member, you will be able to watch technically gifted scientists and commercially astute professionals go from strength to strength under your tutelage. To begin with all structured training will be held in-house, but over time you will source external training providers, some of it online, and factor this into the individuals training requirements. The training itself with cover multiple areas, some with regard to personal improvements such as time management, others will be equipment-specific. Therefore, the need to have at least a fundamental understanding of scientific testing techniques, with knowledge or GMP or GLP being essential for the role. As a result, you are likely to have operated in a laboratory environment already. Diary management and organisation skills are also essential as you will be holding regular, structured reviews with team members and assessing further needs based upon the results. This is a fantastic opportunity to become an integral part of improving an already successful business from within. For more information or to apply, please contact Steve Coomber at Network Scientific. Please note that all applicants for this role should be able to prove that they are legally entitled to work in the UK. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.
Science Solutions Recruitment Ltd
Junior Cosmetic Development Chemist
Science Solutions Recruitment Ltd Bolton, UK
Currently recruiting for an exciting position near Bolton for a Junior Development Chemist. The role will involve working alongside the Laboratory Manager in the development and testing of new and existing cosmetics products, covering the personal, household and car care sectors. You will be required to work in the lab and help cover; formulation development, stability testing, sample preparation, performance testing, regulatory compliance and quality. Essential Experience in a laboratory environment Experience in formulation Understanding of COSHH Strong interpersonal skills to build good working relationship with the laboratory team, and production areas. Ability to work independently and be proactive in your work Desirable Posses the SCS diploma in cosmetic science or a chemistry degree Knowledge of the Cosmetic, Biocidal and Detergent regulations Experience of the CPNP Formulation development within the personal care, household or car industries
Feb 21, 2019
Currently recruiting for an exciting position near Bolton for a Junior Development Chemist. The role will involve working alongside the Laboratory Manager in the development and testing of new and existing cosmetics products, covering the personal, household and car care sectors. You will be required to work in the lab and help cover; formulation development, stability testing, sample preparation, performance testing, regulatory compliance and quality. Essential Experience in a laboratory environment Experience in formulation Understanding of COSHH Strong interpersonal skills to build good working relationship with the laboratory team, and production areas. Ability to work independently and be proactive in your work Desirable Posses the SCS diploma in cosmetic science or a chemistry degree Knowledge of the Cosmetic, Biocidal and Detergent regulations Experience of the CPNP Formulation development within the personal care, household or car industries
VRS Recruitment
Senior Pesticide Residue Analyst/Study Director
VRS Recruitment City Rd, Derby DE1 3RR, UK
Excellent opportunity for an experienced Pesticide Residue Scientist to join a dynamic and expanding CRO! As Study Director you will be the single point of contact, responsible for the successful delivery of projects, on time, within budget and to regulatory guidelines. Utilising your excellent communication skills you must maintain an excellent working relationship with sponsors, ensuring laboratory staff are aware of project timelines and requirements. The position also involves laboratory-based work where you will develop, validate and apply LC-MS/MS methods for pesticide residue analysis. Working in a small team, your responsibilities will encompass the entire study process from sample preparation all the way through to final report. Applications are invited from accomplished Analytical Chemists who have a minimum of 3 years' experience undertaking pesticide residue analysis, ideally within a GLP environment. Experience acting as Study Director would be a distinct advantage although candidates looking to take this next step in their career are also encouraged to apply! If you want the chance to develop your career in a company with an excellent industry reputation and a friendly and flexible work culture, then apply to VRS today! Key words: pesticide residue, agrochemical, agchem, CRO, environmental, LC-MS, LC-MS/MS, HPLC, GC-MS, mass spectrometry, Study Director, GLP, Derby, Midlands, VRS5820AW
Feb 21, 2019
Excellent opportunity for an experienced Pesticide Residue Scientist to join a dynamic and expanding CRO! As Study Director you will be the single point of contact, responsible for the successful delivery of projects, on time, within budget and to regulatory guidelines. Utilising your excellent communication skills you must maintain an excellent working relationship with sponsors, ensuring laboratory staff are aware of project timelines and requirements. The position also involves laboratory-based work where you will develop, validate and apply LC-MS/MS methods for pesticide residue analysis. Working in a small team, your responsibilities will encompass the entire study process from sample preparation all the way through to final report. Applications are invited from accomplished Analytical Chemists who have a minimum of 3 years' experience undertaking pesticide residue analysis, ideally within a GLP environment. Experience acting as Study Director would be a distinct advantage although candidates looking to take this next step in their career are also encouraged to apply! If you want the chance to develop your career in a company with an excellent industry reputation and a friendly and flexible work culture, then apply to VRS today! Key words: pesticide residue, agrochemical, agchem, CRO, environmental, LC-MS, LC-MS/MS, HPLC, GC-MS, mass spectrometry, Study Director, GLP, Derby, Midlands, VRS5820AW
Zenopa
Scientific Sales Specialist
Zenopa City of Leeds, UK
A great opportunity for a Scientist with a background in Nutritional Analysis / Microwave Synthesis / Peptide Synthesis to move into technical scientific sales ! This company is a privately owned a well-respected manufacturer of instrumentation with an excellent market-share in their niche. They provide a truly high quality product line and adopt a very consultative approach when working with customers. PRODUCTS: Microwave Laboratory Instrumentation and Peptide Synthesizers TERRITORY: Northern England and Scotland CLIENTS: Pharmaceutical, Academia, Food & Beverage and Environmental Laboratories The position is around 70-80% field-based travelling to customer sites, with the remainder of your week working from home. Covering Northern England, you will specifically focus on developing and growing sales of peptide synthesizers and will travel to Scotland around a maximum of 1 week per month maximum to grow business, focusing on the full product range. The successful candidate will have the ability to build relationships with lab managers, chemists, analysts and academic groups to position and sell relevant products across customer applications. Responsibilities: Support current users of the company's equipment and develop new business opportunities within the defined sales territory in line with the company's sales and marketing plans. This will be achieved predominately by face to face communication as well as telephone and email-based methods. Ensure an excellent working relationship with staff, customers and future prospects and be capable of working on your own initiative to ensure goals are met for the territory. Ensure excellent administration skills and process all documentation accordingly onto the company's CRM system, this allows future ability to assess strategic and tactical requirements. Ensure excellent communication is maintained with the company's customer care team and inform them of potential issues that have arisen or sales opportunities. Assist the customer care team to solve user application problems when required. Perform instrument demonstrations to customers when required. Handle post purchase installations of equipment at customer sites, providing user training and advising on customer applications. Participate in the company's sales meeting, user group meetings, exhibitions and seminars when required. Ensure excellent knowledge of competitor activity, market trends and information that is valuable for developing your territory. Person Specification: Chemistry or related degree (background in organic or medicinal chemistry) Post-degree experience working in a laboratory and knowledge or experience in Organic/Synthetic/Medicinal Chemistry Excellent communication and organisational skills, experience presenting to large groups. Practically minded, ideally with experience troubleshooting instruments in the laboratory or training junior staff. Drive to succeed in scientific sales and hunger to learn the sales process and products.
Feb 21, 2019
A great opportunity for a Scientist with a background in Nutritional Analysis / Microwave Synthesis / Peptide Synthesis to move into technical scientific sales ! This company is a privately owned a well-respected manufacturer of instrumentation with an excellent market-share in their niche. They provide a truly high quality product line and adopt a very consultative approach when working with customers. PRODUCTS: Microwave Laboratory Instrumentation and Peptide Synthesizers TERRITORY: Northern England and Scotland CLIENTS: Pharmaceutical, Academia, Food & Beverage and Environmental Laboratories The position is around 70-80% field-based travelling to customer sites, with the remainder of your week working from home. Covering Northern England, you will specifically focus on developing and growing sales of peptide synthesizers and will travel to Scotland around a maximum of 1 week per month maximum to grow business, focusing on the full product range. The successful candidate will have the ability to build relationships with lab managers, chemists, analysts and academic groups to position and sell relevant products across customer applications. Responsibilities: Support current users of the company's equipment and develop new business opportunities within the defined sales territory in line with the company's sales and marketing plans. This will be achieved predominately by face to face communication as well as telephone and email-based methods. Ensure an excellent working relationship with staff, customers and future prospects and be capable of working on your own initiative to ensure goals are met for the territory. Ensure excellent administration skills and process all documentation accordingly onto the company's CRM system, this allows future ability to assess strategic and tactical requirements. Ensure excellent communication is maintained with the company's customer care team and inform them of potential issues that have arisen or sales opportunities. Assist the customer care team to solve user application problems when required. Perform instrument demonstrations to customers when required. Handle post purchase installations of equipment at customer sites, providing user training and advising on customer applications. Participate in the company's sales meeting, user group meetings, exhibitions and seminars when required. Ensure excellent knowledge of competitor activity, market trends and information that is valuable for developing your territory. Person Specification: Chemistry or related degree (background in organic or medicinal chemistry) Post-degree experience working in a laboratory and knowledge or experience in Organic/Synthetic/Medicinal Chemistry Excellent communication and organisational skills, experience presenting to large groups. Practically minded, ideally with experience troubleshooting instruments in the laboratory or training junior staff. Drive to succeed in scientific sales and hunger to learn the sales process and products.
Wedding Stationery Artworker
norma dorothy ltd Manchester Central Library, St. Peter's Square, Manchester M2 5PD, UK
norma&dorothy is a paper goods brand based close to Salford Media City. We create rustic inspired hand-crafted stationery, specialising in wedding stationery, gifts and greetings cards. We are currently looking for an enthusiastic and talented wedding stationery artworker to join our team on a full time, permanent basis...... click apply for full job details
Feb 21, 2019
Full time
norma&dorothy is a paper goods brand based close to Salford Media City. We create rustic inspired hand-crafted stationery, specialising in wedding stationery, gifts and greetings cards. We are currently looking for an enthusiastic and talented wedding stationery artworker to join our team on a full time, permanent basis...... click apply for full job details
Quality & Regulatory Affairs Specialist
Genedrive 133 Oldham St, Manchester M4 1LN, UK
THE VISION Genedrive®, is an affordable, real-time PCR system that can serve as the basis for rapid detection, quantification, or drug resistance testing of infectious diseases and pathogens, such as TB or Hepatitis. As we further develop our Point of Care solutions through assay development and product refinement, we have an opportunity to reach millions of people who currently have limited access to existing diagnostic technology. Ultimately, Genedrive has the ability to change lives through rapid access to the benefits of molecular diagnostics. As we ramp up our focus on delivering affordable point of care in vitro molecular diagnostics for addressing global infectious disease challenges, we are looking to strengthen our Quality Team with the addition of another l Quality & Regulatory Affairs Specialist. The Role As one of our Quality & Regulatory Affairs Specialists you will report to our Director of Quality & Regulatory Affairs you will have the following key responsibilities: Participate fully as a member of the Quality Team within and across the business and in particular with our Operations Department; To provide Quality and Regulatory support to all departments within the business; Collaborate with internal and external stakeholders to ensure all our processes comply with the relevant standards and regulations; Collate and provide KPI's, trend data and statistical analysis for Management Review and any other review boards where requested; Provide guidance on Risk Management activities; Provide guidance, support and maintain the Non-Conformance/Deviation system Provide guidance and perform Root Cause Analysis into CAPA investigations Assist in the review of Technical, Medical Device and Design History Files; Create, review, and provide guidance on interpretation of SOP's Review, advise and provide guidance on interpretation of Regulatory requirements; Review Verification and Validation Data Reports and SOP's and provide support during the Validation activities; Provide assistance with the maintenance of the Electronic Quality Management System (Q : Pulse) ; Perform Audits to a predefined schedule Participate and support in external Inspections and Audits with clients, distributors and Notified Bodies; Provide support and guidance for new product development projects; Perform other appropriate duties as assigned. What sort of person are we are looking for? To perform the job successfully, we are looking for an individual who can demonstrate the following competencies: Attention to detail. Organisational and prioritisation skills. Strong written and verbal communication skills. Problem solving. Ability to work alone Ability to work part of a team. Working knowledge of IVDD and/or IVD and ISO 13485 Ideal / Desired Experience & Qualifications: BSc in a Biological Science based degree. Proven experience (3 years or more) of working in Quality Assurance in the IVD or Medical Device Industry W here will I be working? You will be based at our offices at the Incubator Building within the University of Manchester Innovation Centre, on Grafton Street, off Oxford Road in central Manchester. Salary Competitive Salary Hours of Work You will be required to work 37.5 hours per week between the hours of 8.00am and 6.00pm. You can discuss your ideal start and finish times with us. Company Benefits We provide Private Healthcare, Death in Service Benefit, Group Income Protection, Share -Option Scheme, 25 days holiday plus 8 statutory bank holidays) per year, discretionary bonus and a Group Personal Pension scheme. How to apply Please send us a covering letter and cv detailing how your skills and experience match the requirements of the role .
Feb 21, 2019
THE VISION Genedrive®, is an affordable, real-time PCR system that can serve as the basis for rapid detection, quantification, or drug resistance testing of infectious diseases and pathogens, such as TB or Hepatitis. As we further develop our Point of Care solutions through assay development and product refinement, we have an opportunity to reach millions of people who currently have limited access to existing diagnostic technology. Ultimately, Genedrive has the ability to change lives through rapid access to the benefits of molecular diagnostics. As we ramp up our focus on delivering affordable point of care in vitro molecular diagnostics for addressing global infectious disease challenges, we are looking to strengthen our Quality Team with the addition of another l Quality & Regulatory Affairs Specialist. The Role As one of our Quality & Regulatory Affairs Specialists you will report to our Director of Quality & Regulatory Affairs you will have the following key responsibilities: Participate fully as a member of the Quality Team within and across the business and in particular with our Operations Department; To provide Quality and Regulatory support to all departments within the business; Collaborate with internal and external stakeholders to ensure all our processes comply with the relevant standards and regulations; Collate and provide KPI's, trend data and statistical analysis for Management Review and any other review boards where requested; Provide guidance on Risk Management activities; Provide guidance, support and maintain the Non-Conformance/Deviation system Provide guidance and perform Root Cause Analysis into CAPA investigations Assist in the review of Technical, Medical Device and Design History Files; Create, review, and provide guidance on interpretation of SOP's Review, advise and provide guidance on interpretation of Regulatory requirements; Review Verification and Validation Data Reports and SOP's and provide support during the Validation activities; Provide assistance with the maintenance of the Electronic Quality Management System (Q : Pulse) ; Perform Audits to a predefined schedule Participate and support in external Inspections and Audits with clients, distributors and Notified Bodies; Provide support and guidance for new product development projects; Perform other appropriate duties as assigned. What sort of person are we are looking for? To perform the job successfully, we are looking for an individual who can demonstrate the following competencies: Attention to detail. Organisational and prioritisation skills. Strong written and verbal communication skills. Problem solving. Ability to work alone Ability to work part of a team. Working knowledge of IVDD and/or IVD and ISO 13485 Ideal / Desired Experience & Qualifications: BSc in a Biological Science based degree. Proven experience (3 years or more) of working in Quality Assurance in the IVD or Medical Device Industry W here will I be working? You will be based at our offices at the Incubator Building within the University of Manchester Innovation Centre, on Grafton Street, off Oxford Road in central Manchester. Salary Competitive Salary Hours of Work You will be required to work 37.5 hours per week between the hours of 8.00am and 6.00pm. You can discuss your ideal start and finish times with us. Company Benefits We provide Private Healthcare, Death in Service Benefit, Group Income Protection, Share -Option Scheme, 25 days holiday plus 8 statutory bank holidays) per year, discretionary bonus and a Group Personal Pension scheme. How to apply Please send us a covering letter and cv detailing how your skills and experience match the requirements of the role .
Orion Group
Financial Analyst
Orion Group City of Leeds, UK
Orion Group are recruiting a Financial Analyst on behalf of one of our Multinational Medical Device Companies based in the West Yorkshire area on an initial 6 month contract. Role Purpose: Within Commercial Excellence we provide best in class commercial support to both internal stakeholders and external customers, this role delivers aspects of the Pricing functions from the end to end Price Setups (Pricing Cycle), to Price Query Management and issuing Customer Price Reports Key areas of responsibility: Price Setups: · Manage all workflows through the Pricing Cycle (except stage 4) ensuring completeness and accuracy: · Manage the Expiring Discounts pricing process to ensure no expire in error · Maintain up-to-date List Price information on full Product Portfolio · Amend System Price setups for List Prices changes, product substitutes or other changes · If required by the Price Compliance Manager amend system discounts for Contract Management · Ensure all SOX compliance responsibilities are met when offering a Price Price Query Management: · Resolve pricing queries to agreed timelines to ensure customer satisfaction · Process credits where required to resolve pricing queries · Ensure any required remedial action is completed following price queries · Provide pricing intelligence reports to key stakeholders on a monthly basis Customer Price Reports: · Produce detailed Customer Price Reports for Trust's and internal customers following any changes or as requests by stakeholders · Co-ordinate & Produce Annual Pricing catalogues as required · Ensure all Nexus Catalogues for Supplier/Hub or Trust managed arrangements are delivered (PDT) Stakeholder Relationships: · Strong relationships to be formed with Commercial, Product/Marketing and Sales teams · Liaise as required with other departments such as Regulatory, Legal and Finance · Be a part of the wider Commercial Excellence Department · Work with Tender Team and Price Compliance Manager · Maintain strong Customer relationships including any 3rd Party representatives · Maintain strong working relationships with the Price Data Team Desired Experience and Background of the successful candidate · Good understanding of commercial and pricing strategies · Competent in all aspects of Microsoft Office (Excel, Word, Access etc) particularly Excel · High attention to detail and numeric · Excellent communication skills as daily communication with customers, directors, sales force and other line managers - through multiple medias. · Ability to prioritise work on a daily basis. · Team player · 3yrs Prior Experience working within a Pricing or Finance/Commercial Role · Experience using JDE and SAP · Good working knowledge of CM is advantageous · Knowledge of EU Legislation regarding procurement is beneficial 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.
Feb 21, 2019
Orion Group are recruiting a Financial Analyst on behalf of one of our Multinational Medical Device Companies based in the West Yorkshire area on an initial 6 month contract. Role Purpose: Within Commercial Excellence we provide best in class commercial support to both internal stakeholders and external customers, this role delivers aspects of the Pricing functions from the end to end Price Setups (Pricing Cycle), to Price Query Management and issuing Customer Price Reports Key areas of responsibility: Price Setups: · Manage all workflows through the Pricing Cycle (except stage 4) ensuring completeness and accuracy: · Manage the Expiring Discounts pricing process to ensure no expire in error · Maintain up-to-date List Price information on full Product Portfolio · Amend System Price setups for List Prices changes, product substitutes or other changes · If required by the Price Compliance Manager amend system discounts for Contract Management · Ensure all SOX compliance responsibilities are met when offering a Price Price Query Management: · Resolve pricing queries to agreed timelines to ensure customer satisfaction · Process credits where required to resolve pricing queries · Ensure any required remedial action is completed following price queries · Provide pricing intelligence reports to key stakeholders on a monthly basis Customer Price Reports: · Produce detailed Customer Price Reports for Trust's and internal customers following any changes or as requests by stakeholders · Co-ordinate & Produce Annual Pricing catalogues as required · Ensure all Nexus Catalogues for Supplier/Hub or Trust managed arrangements are delivered (PDT) Stakeholder Relationships: · Strong relationships to be formed with Commercial, Product/Marketing and Sales teams · Liaise as required with other departments such as Regulatory, Legal and Finance · Be a part of the wider Commercial Excellence Department · Work with Tender Team and Price Compliance Manager · Maintain strong Customer relationships including any 3rd Party representatives · Maintain strong working relationships with the Price Data Team Desired Experience and Background of the successful candidate · Good understanding of commercial and pricing strategies · Competent in all aspects of Microsoft Office (Excel, Word, Access etc) particularly Excel · High attention to detail and numeric · Excellent communication skills as daily communication with customers, directors, sales force and other line managers - through multiple medias. · Ability to prioritise work on a daily basis. · Team player · 3yrs Prior Experience working within a Pricing or Finance/Commercial Role · Experience using JDE and SAP · Good working knowledge of CM is advantageous · Knowledge of EU Legislation regarding procurement is beneficial 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.
Calibre Search
CAD Manager
Calibre Search Preston, UK
CAD Manager Preston Salary - £35,000 - £50,000 Ref# 16723 Preston based Electrical contractor are in need of a CAD Manager for an available role they have. They are a prominent company in the HV Cable System Solutions. They provide engineering design and build in the HV Substations and Offshore Windfarm sector..... click apply for full job details
Feb 21, 2019
Full time
CAD Manager Preston Salary - £35,000 - £50,000 Ref# 16723 Preston based Electrical contractor are in need of a CAD Manager for an available role they have. They are a prominent company in the HV Cable System Solutions. They provide engineering design and build in the HV Substations and Offshore Windfarm sector..... click apply for full job details
Project Manager - Pharmaceutical
Next Phase Recruitment Limited Alderley Edge SK9, UK
James Hume is recruiting for a Project Manager to join a pioneering Pharmaceutical company who are accelerating the drug discovery process by harnessing new and emerging technologies. The process of developing new medicines is complicated and involves many different stakeholders with different priorities to bring the concept to..... click apply for full job details
Feb 21, 2019
Full time
James Hume is recruiting for a Project Manager to join a pioneering Pharmaceutical company who are accelerating the drug discovery process by harnessing new and emerging technologies. The process of developing new medicines is complicated and involves many different stakeholders with different priorities to bring the concept to..... click apply for full job details
Orion Group
Data Analyst
Orion Group City of Leeds, UK
Orion Group are recruiting for a Data Analyst on behalf of our Multinational Medical Devices Client on an initial 12 month contract based in the West Yorkshire Area Position Purpose Working as part of the Global Demand Planning team to analyse data for the Legal Entity restructuring project. The main aim will be to analyse data sets and highlight key risks and conclusions to ensure the project delivers it commitments. Position Responsibilities Key functions: * Analyse the data from multiple Demand Planning, Supply Planning and Regulatory Affairs data sources along with Master Data inputs to effectively track project performance and risks * Represent Demand Planning on the DiMi project - this will involve interaction with a wide range of stakeholders across Supply Chain and Regulatory teams * Develop strong understanding of the processes that control demand and supply of different product variants for products * Provide back up for Global Demand Plan reporting * Support providing worldwide affiliates supply dates for out of forecast requirements Person Specification Qualifications / Experience: * Strong data analytical skills using a range of platforms * Advanced Excel skills essential * Advanced knowledge of database functionality (Access, SQL) highly desirable * Experience with other data/analytical packages desirable (e.g. Alteryx) * Confident analysing very large data sets from multiple sources and identifying key patterns Values / Behaviours: * Ability to work as part of cross-functional and global team * Ability to interpret data and draw simple conclusions * Must be able to interact and communicate effectively with multiple organisational levels * Motivated and able to learn quickly * A 'team player', happy to support others when required * Analytical and structured approach with a willingness to challenge the status quo * Personable, with good self-awareness * Strong interpersonal and team skills, able to speak up * Ability to work unsupervised * Takes ownership for completion of tasks on time * Works well under pressure with an attention to detail * Willingness to meet global business needs and commitments Position Environment: Key working relationships: * Global Supply Chain Planning Functions * Regulatory Affairs team * Regional Demand Planning Teams: North America, Asia Pacific and Latin America * EMEA market(s): Planning and Commercial teams * Customer Services 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.
Feb 21, 2019
Orion Group are recruiting for a Data Analyst on behalf of our Multinational Medical Devices Client on an initial 12 month contract based in the West Yorkshire Area Position Purpose Working as part of the Global Demand Planning team to analyse data for the Legal Entity restructuring project. The main aim will be to analyse data sets and highlight key risks and conclusions to ensure the project delivers it commitments. Position Responsibilities Key functions: * Analyse the data from multiple Demand Planning, Supply Planning and Regulatory Affairs data sources along with Master Data inputs to effectively track project performance and risks * Represent Demand Planning on the DiMi project - this will involve interaction with a wide range of stakeholders across Supply Chain and Regulatory teams * Develop strong understanding of the processes that control demand and supply of different product variants for products * Provide back up for Global Demand Plan reporting * Support providing worldwide affiliates supply dates for out of forecast requirements Person Specification Qualifications / Experience: * Strong data analytical skills using a range of platforms * Advanced Excel skills essential * Advanced knowledge of database functionality (Access, SQL) highly desirable * Experience with other data/analytical packages desirable (e.g. Alteryx) * Confident analysing very large data sets from multiple sources and identifying key patterns Values / Behaviours: * Ability to work as part of cross-functional and global team * Ability to interpret data and draw simple conclusions * Must be able to interact and communicate effectively with multiple organisational levels * Motivated and able to learn quickly * A 'team player', happy to support others when required * Analytical and structured approach with a willingness to challenge the status quo * Personable, with good self-awareness * Strong interpersonal and team skills, able to speak up * Ability to work unsupervised * Takes ownership for completion of tasks on time * Works well under pressure with an attention to detail * Willingness to meet global business needs and commitments Position Environment: Key working relationships: * Global Supply Chain Planning Functions * Regulatory Affairs team * Regional Demand Planning Teams: North America, Asia Pacific and Latin America * EMEA market(s): Planning and Commercial teams * Customer Services 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.
Junior Data Scientist
Oscar Associates (UK) Limited Derby, UK
Data Scientist- Derby- Manchine learning, Python, R- £30,000 The Role We are looking for a junior data scientist to join the Derby office. The successful candiate will be welcomed into a friendly and supportive team, with the opportunity to take complex data and make it valuable/accessible to all levels of..... click apply for full job details
Feb 21, 2019
Full time
Data Scientist- Derby- Manchine learning, Python, R- £30,000 The Role We are looking for a junior data scientist to join the Derby office. The successful candiate will be welcomed into a friendly and supportive team, with the opportunity to take complex data and make it valuable/accessible to all levels of..... click apply for full job details
Marketplace Group
Stability Coordinator
Marketplace Group North Cheshire Motorway, High Legh, Knutsford WA16 0SF, UK
Leading Pharmaceutical Manufacturer based in Cheshire seeks an experienced Stability Coordinator. About the role: The receipt, logging, labelling and set down of stability samples, whether from internal or external sources. Sample pulls, and arrangement of transport, where required, to other sites. Generation of Stability Protocols, workbooks and specifications as required. Checking, collation and reporting of test data. Generation and assessment of trend data for studies. Duties may include: Generation and management of stability protocols Maintenance and adherence of the stability schedule Receipt and despatch of stability samples from other business units within the group Maintenance housekeeping of the stability chambers and associated facilities Point of contact for maintenance of chambers Maintain records of samples and ensure accurate reconciliation of samples Support any technical reports required associated with stability Serve as the central point of contact for all product stability program activities on the site and liasing with other sites to meet their requirements. Coordinate all stability program activities in the site. Develop and maintain a detailed understanding of all government regulations regarding all aspects of stability testing Develop and maintain a detailed understanding of all corporate policies and procedures regarding stability testing Aid in regulatory audits on all matters relating to product stability. Draft and maintain stability program policies and procedures as necessary to maintain compliance Help establish and monitor stability related Quality Assurance programs and procedures to ensure compliance Advise management on any corrective action required to maintain regulatory compliance with stability regulations and guidelines Ensure the performance of periodic review of stability program Skills and experience: Knowledge/understanding of GMP Work experience in a laboratory environment Knowledge of GLP Degree in relevant scientific discipline
Feb 21, 2019
Leading Pharmaceutical Manufacturer based in Cheshire seeks an experienced Stability Coordinator. About the role: The receipt, logging, labelling and set down of stability samples, whether from internal or external sources. Sample pulls, and arrangement of transport, where required, to other sites. Generation of Stability Protocols, workbooks and specifications as required. Checking, collation and reporting of test data. Generation and assessment of trend data for studies. Duties may include: Generation and management of stability protocols Maintenance and adherence of the stability schedule Receipt and despatch of stability samples from other business units within the group Maintenance housekeeping of the stability chambers and associated facilities Point of contact for maintenance of chambers Maintain records of samples and ensure accurate reconciliation of samples Support any technical reports required associated with stability Serve as the central point of contact for all product stability program activities on the site and liasing with other sites to meet their requirements. Coordinate all stability program activities in the site. Develop and maintain a detailed understanding of all government regulations regarding all aspects of stability testing Develop and maintain a detailed understanding of all corporate policies and procedures regarding stability testing Aid in regulatory audits on all matters relating to product stability. Draft and maintain stability program policies and procedures as necessary to maintain compliance Help establish and monitor stability related Quality Assurance programs and procedures to ensure compliance Advise management on any corrective action required to maintain regulatory compliance with stability regulations and guidelines Ensure the performance of periodic review of stability program Skills and experience: Knowledge/understanding of GMP Work experience in a laboratory environment Knowledge of GLP Degree in relevant scientific discipline
Penguin Recruitment
Building Physicist
Penguin Recruitment Sheffield, UK
Building Physicist £35,000 per annum + benefits Ref: SH376 Penguin Recruitment is delighted to be working with a leading building services design engineering consultancy currently looking for a Building Physicist to join their team based in Sheffield. You will be joining a well-established..... click apply for full job details
Feb 21, 2019
Full time
Building Physicist £35,000 per annum + benefits Ref: SH376 Penguin Recruitment is delighted to be working with a leading building services design engineering consultancy currently looking for a Building Physicist to join their team based in Sheffield. You will be joining a well-established..... click apply for full job details
Tangerine Holdings Limited
Regulatory Affairs Associate/Executive
Tangerine Holdings Limited Lytham Saint Annes FY8, UK
Regulatory Affairs Associate/Executive £18,000 - £27,000 Lytham About The Role We currently have an excellent opportunity for a Regulatory Affairs Associate/Executive to join our head office in Lytham, Lancashire on a permanent basis. Reporting to the Head of Regulatory Affairs, you will play a key role in supporting the day to day activity that drives our Regulatory team to keep our brands safe and legal. You'll work closely with the Hiring Manager to oversee that requests for information, product labelling and standard operating procedures are up to date and in line with everything we do or we're about to do! The Regulatory Affairs Associate/Executive will work within the Regulatory affairs team to support the implementation and management of the regulatory status for all products within the Tangerine Group. Duties and responsibilities will include but not be limited to: Regulatory Affairs Associate/Executive About You Previous experience within a Regulatory environment (Desirable not Essential) You should have attained a 2:1 or higher in a Bachelor of Science subject, ideally Chemistry or Biology. You'll be fanatical in relation to attention to detail, as in this role the detail really does count. You should possess excellent verbal and oral communication skills as well as prioritisation skills. Why? Well, in this role you are the glue that holds everything together, but you could also be the blocker to manufacturing our products if you're not working closely with our other teams. Roles/Responsibilities You will; Ensure that all product labels, literature and packaging comply with the appropriate legislation (e.g. Equine prohibited Substances, Feeding Stuffs Regulations, Veterinary Medicines Regulations guidelines) in both UK and international markets. Assist with collating, preparing and progressing UK product renewals and variations for existing Marketing Authorisations. Oversee and perform continuous analysis on existing dossiers and update regulatory compliance documents to ensure all product registrations are current and compliant in each country. Create and produce regulatory dossiers for registration and export of products to international markets. Provide continuous support to the International Distributors Maintain a system to track all relevant stages of registration and licensing. Work closely with the Quality department to ensure that any changes are made in line with regulatory requirements. Provide project updates to the Head of Regulatory Affairs. To support Customer Services in providing required documentation for international orders (i.e. Certificates of Analysis, Health Certificates, Certificates of Free Sale Oversee to ensure Safety Data Sheets (MSDS) are up to date and in line with current regulations for all products within the Tangerine Group. Other projects as directed by the Head of Regulatory Affairs Create and maintain appropriate tracking systems for changes to registrations Your personality is what really counts with us, ambition, drive, determination will make you stand out at Tangerine! The Benefits Competitive salary and benefits package Holidays that increase with length of service Personal and Professional development Pension Bonus and Health cover (after qualifying period) About Us The Tangerine Group is a privately held company based in Lytham. Within the group are ten limited companies, each operating as stand-alone entities. We specialise in the manufacture and sales of animal health and nutrition products for farm and companion animals, including veterinary and equine products. We are currently the 2nd biggest manufacturer of Veterinary Nutraceuticals in the world. In addition, we currently distribute to 40 countries in the world and looking to increase this to 80 in the next 5 years. Interested? Apply online for immediate consideration
Feb 21, 2019
Regulatory Affairs Associate/Executive £18,000 - £27,000 Lytham About The Role We currently have an excellent opportunity for a Regulatory Affairs Associate/Executive to join our head office in Lytham, Lancashire on a permanent basis. Reporting to the Head of Regulatory Affairs, you will play a key role in supporting the day to day activity that drives our Regulatory team to keep our brands safe and legal. You'll work closely with the Hiring Manager to oversee that requests for information, product labelling and standard operating procedures are up to date and in line with everything we do or we're about to do! The Regulatory Affairs Associate/Executive will work within the Regulatory affairs team to support the implementation and management of the regulatory status for all products within the Tangerine Group. Duties and responsibilities will include but not be limited to: Regulatory Affairs Associate/Executive About You Previous experience within a Regulatory environment (Desirable not Essential) You should have attained a 2:1 or higher in a Bachelor of Science subject, ideally Chemistry or Biology. You'll be fanatical in relation to attention to detail, as in this role the detail really does count. You should possess excellent verbal and oral communication skills as well as prioritisation skills. Why? Well, in this role you are the glue that holds everything together, but you could also be the blocker to manufacturing our products if you're not working closely with our other teams. Roles/Responsibilities You will; Ensure that all product labels, literature and packaging comply with the appropriate legislation (e.g. Equine prohibited Substances, Feeding Stuffs Regulations, Veterinary Medicines Regulations guidelines) in both UK and international markets. Assist with collating, preparing and progressing UK product renewals and variations for existing Marketing Authorisations. Oversee and perform continuous analysis on existing dossiers and update regulatory compliance documents to ensure all product registrations are current and compliant in each country. Create and produce regulatory dossiers for registration and export of products to international markets. Provide continuous support to the International Distributors Maintain a system to track all relevant stages of registration and licensing. Work closely with the Quality department to ensure that any changes are made in line with regulatory requirements. Provide project updates to the Head of Regulatory Affairs. To support Customer Services in providing required documentation for international orders (i.e. Certificates of Analysis, Health Certificates, Certificates of Free Sale Oversee to ensure Safety Data Sheets (MSDS) are up to date and in line with current regulations for all products within the Tangerine Group. Other projects as directed by the Head of Regulatory Affairs Create and maintain appropriate tracking systems for changes to registrations Your personality is what really counts with us, ambition, drive, determination will make you stand out at Tangerine! The Benefits Competitive salary and benefits package Holidays that increase with length of service Personal and Professional development Pension Bonus and Health cover (after qualifying period) About Us The Tangerine Group is a privately held company based in Lytham. Within the group are ten limited companies, each operating as stand-alone entities. We specialise in the manufacture and sales of animal health and nutrition products for farm and companion animals, including veterinary and equine products. We are currently the 2nd biggest manufacturer of Veterinary Nutraceuticals in the world. In addition, we currently distribute to 40 countries in the world and looking to increase this to 80 in the next 5 years. Interested? Apply online for immediate consideration
Morson Human Resources Limited
Lead Draughtsman
Morson Human Resources Limited Derbyshire, UK
Our Client is a provider of Engineering Design and Build solutions to a variety of Markets including Nuclear, Chemical, Gas and General Engineering sectors. They require an experienced drawing office lead to manage the delivery of compliant drawings and models to meet project d... ..... click apply for full job details
Feb 21, 2019
Full time
Our Client is a provider of Engineering Design and Build solutions to a variety of Markets including Nuclear, Chemical, Gas and General Engineering sectors. They require an experienced drawing office lead to manage the delivery of compliant drawings and models to meet project d... ..... click apply for full job details
VRS Recruitment
Technical Director - Analytical Chemistry
VRS Recruitment Manchester Central Library, St. Peter's Square, Manchester M2 5PD, UK
Fantastic opportunity for an accomplished Analytical Chemist - with extensive hands-on Mass Spectrometry expertise - to lead our client's R&D studies at their highly innovative analytical testing laboratory! Reporting directly to board-level, you will provide technical direction, analytical expertise and project guidance across various cutting-edge application areas. You will research, develop and implement investigative programs to bolster and grow the company's reputation as the 'go to' lab for challenging small molecule Mass Spec applications. Your team will undertake novel research - presenting and publishing worldwide. You will also provide expert guidance and direction to analytical teams and clients on technical issues, supporting in method development and validation. Experience of quantitative analysis by LC-MS and GC-MS is key - team leadership skills are beneficial as you will mentor one direct report. Applications are invited from candidates who can demonstrate the following: Expertise with LC-MS and GC-MS for small molecule applications Extensive method development experience Excellent research and analytical problem-solving skills Strong communication skills Apply today to learn more about this unique opportunity! Keywords: HPLC, UPLC, LC-MS, GC-MS, mass spectrometry, high resolution, HRMS, High Res, Q-ToF, GLP, GMP, method development, small molecules, extractables, leachables, argochem, validation Manchester, VRS6189DJ
Feb 21, 2019
Fantastic opportunity for an accomplished Analytical Chemist - with extensive hands-on Mass Spectrometry expertise - to lead our client's R&D studies at their highly innovative analytical testing laboratory! Reporting directly to board-level, you will provide technical direction, analytical expertise and project guidance across various cutting-edge application areas. You will research, develop and implement investigative programs to bolster and grow the company's reputation as the 'go to' lab for challenging small molecule Mass Spec applications. Your team will undertake novel research - presenting and publishing worldwide. You will also provide expert guidance and direction to analytical teams and clients on technical issues, supporting in method development and validation. Experience of quantitative analysis by LC-MS and GC-MS is key - team leadership skills are beneficial as you will mentor one direct report. Applications are invited from candidates who can demonstrate the following: Expertise with LC-MS and GC-MS for small molecule applications Extensive method development experience Excellent research and analytical problem-solving skills Strong communication skills Apply today to learn more about this unique opportunity! Keywords: HPLC, UPLC, LC-MS, GC-MS, mass spectrometry, high resolution, HRMS, High Res, Q-ToF, GLP, GMP, method development, small molecules, extractables, leachables, argochem, validation Manchester, VRS6189DJ
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