Location - UK, Field-Based Would you like to work for a rapidly expanding microbiological service company? Do you have a good understanding of the pharmaceutical market? Are you educated with a life sciences background? We are working with a successful and ambitious microbiology service company who provides microbiology, analytical and biological storage services to a wide range of industries to recruit a Business Development Manager into the business. The successful candidate will be highly motivated and looking to play an integral part in the realisation of a company's growth plans. The post presents an excellent opportunity for someone with previous business development experience in the life sciences (microbiology, genomics or sequencing) area to join a great team who are proud of their past and excited about their future. Key responsibilities and competencies include: Create and deliver a business development strategy for annual double-digit growth across the company. Proactively account manage and develop strong business relationships with current and new customers. Build a distributor network for core products, while maintaining and strengthening existing distributor relationships. Fully understand the company's business reach and deliver compelling propositions that demonstrate the benefits and impacts of their offerings to the customer's business. Effectively manage the sales pipeline to increase growth and market share in the UK and International markets. Visit customers and represent the company at external meetings and events. The ideal candidate will be educated to degree level preferably with a life sciences background and formal qualifications in life sciences and/or business and marketing related subject areas. You will understand the life sciences market (preferably with a focus on microbiology, genomics or sequencing) and be highly competent at researching and engaging with organisations to deliver priority leads. In return you will enjoy working within a close, friendly and inclusive environment where your successes will be appreciated and celebrated. An attractive salary and benefits package are available.

This well-established water treatment/hygiene company currently has a vacancy for a competent and experienced Legionella Risk Assessor to join them working on a variety of contracts in and around the North West region. Applications from Manchester, Cheshire, Lancashire, Merseyside and the surrounding areas will be considered. Qualifications & Experience: Must hold relevant Legionella Risk Assessment qualification such as City & Guilds or equivalent. Extensive experience carrying out risk assessments on hot and hot water services, industrial systems, etc. A strong working knowledge relating to ACOP L8. Excellent communication skills, both written and verbal. Proficient in using the Microsoft Office Package. Role: Carrying out Legionella Risk Assessments in line with ACOP L8 on a wide range of properties including industrial and commercial. Compiling schematic drawings and producing final documents for clients. Providing recommendations and prices for remedial works, routine control measures through to quotations and carrying out such works based on the risk assessments. Monthly temperature testing, monitoring and water sampling. Surveying of water systems and supplies. Attending meetings with clients as and when required. Maintain a professional working relationship with clients. This company is offering an attractive salary, depending on experience, company vehicle and many other benefits to the right candidate. Future Select are recruiting in the Water Treatment/Hygiene industry; we work with the best clients & candidates and supply the majority of permanent jobs in the market. We would be interested in speaking to candidates with experience in any disciplines from Risk Assessors, Service Engineers, Account Managers and Business Development/Operational Managers through to Director level. We are inundated with applications, we will endeavour to get back in touch, however if you have applied to Future Select and you have not heard from us after a week, on this occasion, you will not have been successful. Your details will be saved on our system and you will be contacted in the future if a vacancy matches your skills. Future Select Copyright 2019.

If you had the opportunity to work from home would you take it? Of course you would… so read on… Due to continued growth my client, a market leading organisation in the healthcare ecosystem are seeking an experienced contracts and proposals manager to support a newly created business development function. As the contracts and proposals manager you will support this developing function by responding to RFPs, RFIs and budget requests from clients. In addition, you will support the development and review of contracts. If you are a self-starter, enthusiastic and knowledgeable with a keen eye for detail then this role is tailor made for you. Obviously, there is a lot more to it, but where would the fun be in giving everything away in an advert! I want to hear from you if you have demonstrable experience in either the biotechnology, pharmaceutical or medical device arena. These opportunities don't come around often (did I mention you get to work from home?!) so if you want to learn more, please give me a call or apply below and a member of the executive team will be in touch. With offices in Cambridge, Northampton and Peterborough - The ONE Group's recruitment specialists offer unparalleled recruitment expertise across seven specialist divisions; Accountancy & Finance, Executive Search, HR, IT, Marketing, Office Support and Technical. Whether you are looking to advertise a job, or take the next step in your career, we offer an ever-growing employment network, which currently exceeds 50,000 people in the East of England and The Midlands. We pride ourselves in adding value to any recruitment experience, with the foundation of our success coming from customer service, expert knowledge of the local marketplace and our understanding of the significant value people can add to the workplace. This isn't just recruitment, it's Recruitment as it should be.

Technical Change Lead - Contract. Your new company Our Private sector pharmaceutical organisation is looking for a Technical Change Lead Your new role Technical Change Lead, Responsible for a work stream within the Business Deployment team. What you'll need to succeed Previous experience supporting Automation and IT technology. Experience of working within Pharmaceuticals. Expertise in Level 4 global trace ability systems Good understanding of trace ability at site and global level Understanding of trace ability legislation SAP ATTP Strong project management capability with demonstrable experience of managing project work streams. Desirable Working knowledge of G1 Standards. Experience working with IT solutions (i.e ATTP, Aii, ERP, MDM applications) Knowledge of network segmentation and security. What you'll get in return A 6-9 month contract working for a global organisation with a good rate of pay. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk

Regulatory and Quality Officer A new opportunity for a Regulatory and Quality Officer has recently become available to join an international medical device company that are leading the way in biological technology. As a Regulatory and Quality Officer you will support the RA/QA Manager in maintaining a QMS that meets the applicable regulatory and company requirements (such as ISO 13485, EU Medical Device Directive/Regulation (MDD/MDR), EN/IEC 62304, ISO 14971, etc.) * You will support in product submissions, licence renewals, periodic updates and registrations to regulatory agencies (FDA and EU regulatory entities) * Assist in the creation and review of design dossiers technical files, and Product Approval Certificates. * Update and maintain all Design History Files and associated documents. * Coordination of post-market activities e.g. surveillance, customer feedback, failure analysis. * Update and review all IFU, Packaging, Labelling and Art Work approval. We are interested in speaking to individuals who have experience within the medical device, pharmaceutical or cosmetics industry. Ideally educated to honours degree level in a scientific field or equivalent experience. You will be efficient, well organised and have a systematic and methodical approach to work. Key Words: Regulatory Affairs, QA, Quality Assurance, Medical Device, Technical Files, Design History Files, ISO 13485, Post Market Surveillance, Art Work approval, QMS. 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.

This is a great opportunity for a R&D Synthetic Chemist with some prior industrial experience of organic chemistry to join a speciality chemical firm in the greater Birmingham area. The R&D Synthetic Chemist role is ideal for recent graduates in a relevant chemistry field with a placement year within industry, or more experienced chemical professionals, and the successful appointment will be able to build a broad process-related skillset for excellent career progression potential. Your day to day duties as a R&D Synthetic Chemist will be: Researching and developing routes from lab to plant scale manufacture of chemical products Use of common analytical methods towards in-process and quality control procedures Liaising with production staff to ensure reproducibility Research into new revenue streams You will be an ideal candidate with this background: A degree, or higher, in a chemistry-related field A track record in synthetic chemistry in the laboratory This client is already shortlisting for the role so I would like you to apply immediately with a CV (Word document format, 2 pages maximum) so as to not miss out on the opportunity. Note my client is unable to sponsor visas for those without eligibility to work in the UK. Why should you work with Dr Paul Mears as your scientific specialist recruiter at Science Solutions? I focus solely on matching scientists to positions in the UK speciality chemical industry, which is where my own experience and network position me best given a background working in the speciality chemicals and fragrance and flavours sectors. I completed academic studies with a PhD in organic chemistry at the University of Manchester, which followed a BSc in the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up three years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.

This well-established water treatment/hygiene company currently has a vacancy for a competent and experienced Legionella Risk Assessor to join them working on a variety of contracts in and around the North West region. Applications from Manchester, Cheshire, Lancashire, Merseyside and the surrounding areas will be considered. Qualifications & Experience: Must hold relevant Legionella Risk Assessment qualification such as City & Guilds or equivalent. Extensive experience carrying out risk assessments on hot and hot water services, industrial systems, etc. A strong working knowledge relating to ACOP L8. Excellent communication skills, both written and verbal. Proficient in using the Microsoft Office Package. Role: Carrying out Legionella Risk Assessments in line with ACOP L8 on a wide range of properties including industrial and commercial. Compiling schematic drawings and producing final documents for clients. Providing recommendations and prices for remedial works, routine control measures through to quotations and carrying out such works based on the risk assessments. Monthly temperature testing, monitoring and water sampling. Surveying of water systems and supplies. Attending meetings with clients as and when required. Maintain a professional working relationship with clients. This company is offering an attractive salary, depending on experience, company vehicle and many other benefits to the right candidate. Future Select are recruiting in the Water Treatment/Hygiene industry; we work with the best clients & candidates and supply the majority of permanent jobs in the market. We would be interested in speaking to candidates with experience in any disciplines from Risk Assessors, Service Engineers, Account Managers and Business Development/Operational Managers through to Director level. We are inundated with applications, we will endeavour to get back in touch, however if you have applied to Future Select and you have not heard from us after a week, on this occasion, you will not have been successful. Your details will be saved on our system and you will be contacted in the future if a vacancy matches your skills. Future Select Copyright 2019.

Regulatory and Quality Officer A new opportunity for a Regulatory and Quality Officer has recently become available to join an international medical device company that are leading the way in biological technology. As a Regulatory and Quality Officer you will support the RA/QA Manager in maintaining a QMS that meets the applicable regulatory and company requirements (such as ISO 13485, EU Medical Device Directive/Regulation (MDD/MDR), EN/IEC 62304, ISO 14971, etc.) * You will support in product submissions, licence renewals, periodic updates and registrations to regulatory agencies (FDA and EU regulatory entities) * Assist in the creation and review of design dossiers technical files, and Product Approval Certificates. * Update and maintain all Design History Files and associated documents. * Coordination of post-market activities e.g. surveillance, customer feedback, failure analysis. * Update and review all IFU, Packaging, Labelling and Art Work approval. We are interested in speaking to individuals who have experience within the medical device, pharmaceutical or cosmetics industry. Ideally educated to honours degree level in a scientific field or equivalent experience. You will be efficient, well organised and have a systematic and methodical approach to work. Key Words: Regulatory Affairs, QA, Quality Assurance, Medical Device, Technical Files, Design History Files, ISO 13485, Post Market Surveillance, Art Work approval, QMS. 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.

Research Scientist - Chemicals / Polymers / Rubber My client is an international market leader in the manufacture and supply of high quality, industrial sealing products. They now require a Research Scientist to assist in new product development and research new technology that contributes to the growth requirements of the business. The role will also require some commercial contact with new and existing customers, especially with regard to new products, particularly during the later stages of development. The Role: * You will be responsible to assist in reviewing ideas and developing potential new products, carry out formulation experiments, including physical testing of prototypes. * You will conduct test protocols and procedures, and product evaluation. * Assist with introduction of new products as required, including working with Production Engineers and Production Operatives during a product scale up/handover. The Candidate: * BSc in Chemistry or Materials Science or Polymer Chemistry based degree * The role will include formulation of products containing rubbers or polymers; therefore knowledge of rubber or polymer chemistry will be an advantage. * Experience in formulation using bulk chemicals would be desirable. * Knowledge and experience in a range of chemical analytical techniques would also be preferable. 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.

Company: Ashfield Healthcare Position: Healthcare Assistant- Phlebotomist Territory: Yorkshire Vacancy: Permanent Salary: Competitive Ashfield Healthcare is currently recruiting for a Healthcare Assistant- Phlebotomist to work on an exciting programme which will involve patient home visits to..... click apply for full job details

Quality Manager - Dundee Salary - Circa £39k + Pension + Healthcare + Childcare + Vouchers + Gym Membership The Client Our client is a knowledge based, science led business focused on delivering the services, expertise and capabilities to their clients. Their business is focused on a number of core sectors including pharmaceutical, biotechnology, food, environmental, agrochemical, petrochemical, chemical and consumer products industries. They support drug research, discovery and development to their pharmaceutical and biotechnology clients; provide testing and specialist analytical services and consultancy to the pharmaceutical, food and environmental sectors, toxicology services to the pharmaceutical, chemical, agrochemical and consumer products industries and materials chemistry services to the petrochemical industry. The company currently employs over 800 employees across 11 main sites in the U.K. The Role An opportunity has arisen to join our client's team, in Dundee, as Quality Manager. Due to substantial business growth and in order to enhance their client services, they have recently expanded their Regulatory Good Laboratory Practice (GLP) services at the Dundee site. The successful candidate will be required to further develop and maintain the Quality Assurance Programme for GLP and GCP and perform the independent monitoring for compliance with the current regulations. This role is also required to take the lead and train operational staff in the requirements of GLP and GCP. Main Duties: The QM's function is the independent Good Laboratory Practice (GLP) monitoring of work conducted as required by the regulatory guidelines employed therein. The QM is responsible for the day to day management of QA. In addition, audits may be required to be performed at other sites as well as Suppliers and Subcontractors. To do this the Quality Manager shall: Assume responsibility for the maintenance of the quality assurance programme in accordance with current regulations and guidance Assume responsibility for the day to day management of QA functions Perform all aspects of GLP and GCP monitoring of work conducted Review the Quality Assurance programme to ensure it meets regulatory requirements and is of maximum benefit, reporting any deficiencies to the Group Head of Quality Assurance and Test Facility Management. Develop or improve in conjunction with the Group Head of Quality Assurance auditing strategies for new systems introduced at Dundee or other sites as required Working with site Management to ensure GLP/GCP standards are maintained Develop in conjunction with the Group Head of Quality Assurance and deliver formal GLP and GCP training Act as QA contact for site SUMMARY OF DUTIES AND RESPONSIBILITIES: Review Study Plans for compliance with GLP/GCP where required Write and review Quality Assurance Standard Operating Procedures Review Standard Operating Procedures for compliance with principles of GLP/GCP Schedule, conduct and report audits as required, this will include but not be limited to: Study/Analytical phases SOPs Standard forms/templates Computer system validation Suppliers/Subcontractors Advise management of any deficiencies in Regulatory Requirements Host or partake in Sponsor and Regulatory visits Liaise with site personnel to ensure a full understanding of regulatory requirements. Train other personnel in all aspects of Quality Assurance Systems and Procedures as required Perform administrative tasks as required. Skills and Experience BSc in Biology or related subject Proven knowledge, skills and abilities in managing GLP auditing and Regulatory Requirements Preferably experience of GCP within analytical laboratories Excellent organisational, interpersonal and communication skills. Competent at preparing and delivering presentations to employees, customers and regulatory bodies. Strong management skills and ability to lead a team through change. Proven ability to challenge and drive quality and a compliant culture forward. Experience in influencing, impacting and leading QA operations through developing audit schedules, training initiatives, QA recruitment. Ability to investigate and review information and draw conclusions in support of CAPA, deviations etc. The company offer a range of learning and development opportunities depending on the role, with all employees having access to a range of internally delivered training modules as standard. In their science based roles they offer structured career progression, more details of which can be discussed during the recruitment process. In addition to a competitive salary, they offer as a minimum: Pension scheme, Healthcare Cash Plan, Retail Discount scheme, Cycle to Work scheme, Childcare Vouchers, Discounted Gym membership rates and local Reward & Recognition schemes. Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Additional Resources will be acting in your best interest and may contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy 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 GDPR please contact us. Additional Resources are an Employment Business and an Employment Agency as defined within The Conduct of Employment Agencies & Employment Businesses Regulations 2003.

Quality Manager - ISO 17025 & GMP - Manchester Salary - Circa £50k + Pension + Healthcare + Childcare + Vouchers + Gym Membership The Client Our client is a knowledge based, science led business focused on delivering the services, expertise and capabilities to their clients. Their business is focused on a number of core sectors including pharmaceutical, biotechnology, food, environmental, agrochemical, petrochemical, chemical and consumer products industries. They support drug research, discovery and development to their pharmaceutical and biotechnology clients; provide testing and specialist analytical services and consultancy to the pharmaceutical, food and environmental sectors, toxicology services to the pharmaceutical, chemical, agrochemical and consumer products industries and materials chemistry services to the petrochemical industry. The company currently employs over 800 employees across 11 main sites in the U.K. The Role This is an opportunity to join the Analytical and Development Services Division in the role of Quality Manager across the groups UKAS ISO 17025 and GMP divisions. The role currently encompasses 6 sites across the UK and requires regular travel to those sites. The successful candidate would be required to take the lead in ensuring that the demands of both customers and certifying bodies/ regulators are met and that a consistent approach to quality-based processes is achieved. The role requires leading the transition to ISO17025:2017 during 2018/2019. Main Duties to: Lead the existing QA team across the company's locations, at sites across the UK, to provide compliance oversight of GMP and ISO regulated activities. Fulfil the role of Group UKAS Quality Manager, in accordance with 17025 requirements Work with the other Quality Managers within the company to ensure a consistent approach to Quality is maintained across the company. Host Accreditation and Regulatory Inspections Develop auditing strategies to ensure the company meet the requirements of the regulations & accreditations held Ensure that the systems and resources in place currently, and those that are developed, make efficient use of employees and are compliant with all regulatory and accreditation demands. Monitor the performance and develop your QA team, and ensure that they have adequate training to complete their duties. Lead customer audits, where it is appropriate, to ensure the best possible outcome for the business in maintaining the customer's confidence in the company's services. Work with business development and operational staff to ensure that data quality and integrity is embedded into all the business does. Work in harmony with all employees to keep them engaged with the quality objectives of the company and foster effective communication between departments. Work with existing and developing systems to be able to report on quality related matters to the board in a timely manner. Remain current with compliance related developments and ensure that potential impacts are communicated to all relevant departments. Aid with the implementation of electronic QMS Assess problems pragmatically and assess risk and escalate as appropriate. Advise Management of any deficiencies in Accreditation or Regulatory requirements Qualifications/Role Requirements: A graduate with substantial experience in the testing and contract research/pharmaceutical industry working to ISO 17025, in a Quality Management role. Experience in a high throughput environment would be an advantage. Thorough knowledge, skills and abilities in managing ISO 17025, GMP Standards, guidance and regulations. Proven knowledge and experience of scheduling and performing audits. Experience in hosting/supporting customer, accreditation and regulatory agency inspections, in particular, understanding the requirements of UKAS. Excellent organisational, interpersonal and communication skills. Competent at preparing and delivering presentations to employees, customers and regulatory bodies. Strong management skills and ability to lead a team through change. Proven ability to challenge and drive quality and a compliant culture forward. Experience in influencing, impacting and leading QA operations through developing audit schedules, training initiatives, QA recruitment. Ability to investigate and review information and draw conclusions in support of CAPA, customer complaints etc. Travel within the UK is required on a regular basis The company offer a range of learning and development opportunities depending on the role, with all employees having access to a range of internally delivered training modules as standard. In their science based roles they offer structured career progression, more details of which can be discussed during the recruitment process. In addition to a competitive salary, they offer as a minimum: Pension scheme, Healthcare Cash Plan, Retail Discount scheme, Cycle to Work scheme, Childcare Vouchers, Discounted Gym membership rates and local Reward & Recognition schemes. Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Additional Resources will be acting in your best interest and may contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy 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 GDPR please contact us. Additional Resources are an Employment Business and an Employment Agency as defined within The Co

Due to team expansion another research scientist position is available within Clinical Biochemistry R&D. The successful candidate will be involved in the development and improvement of antibody/protein reagents and analytical systems for our portfolio and pipeline products. The main responsibilities are to perform laboratory experiments as directed by the Project Leader and to record data in compliance with the company quality policy. Working in a multi-disciplinary team environment, the successful candidate will be expected to make scientific and intellectual contributions to product/assay development. The main duties of the role are: • To perform new product feasibility studies, including design and testing of novel reagents and protocols. • To validate new procedures and materials up to the point of technology transfer to other departments. • To assess new materials and laboratory equipment, and give feedback on their suitability for use. • To perform scientific calculations, including molar and unit conversions, reaction kinetics, purity assessments and clinical statistical analyses. • To develop technical expertise in a broad spectrum of disciplines including (but not limited to): protein/antibody purification and analysis, automated preparative and analytical systems and immunoassay (multiple formats). • To carry out design changes to existing products and processes when required. • To generate clear and accurate experimental records and present findings in project and departmental meetings. Knowledge and Skills Essential: • Degree in Biochemistry or related discipline. • Experience of protein and biochemical analyses. • Hands-on laboratory experience gained during degree projects, placements or post-graduation employment. • Passionate about biochemical/analytical sciences with a desire to work in a dynamic research environment. • To be reliable and flexible to the needs of the business. Desirable: • Previous industrial experience in healthcare or medical diagnostics sector. • Working knowledge of protein purification (including chromatography systems) and/or bio-conjugation. • Experience of technology development. • Master's degree in Biochemistry or protein sciences.