• Method Development Chemist 12/4/2017 12:00:00 AM

    Salary: £0 Location: SKIPTON

    The Client A privately-owned global analytical services business my client is an FDA and MHRA inspected laboratory focused on delivering a high-quality service for industry-leading clients across the pharmaceutical, animal health, medical device and electronic nicotine delivery industries. The Role As an Analytical Development Scientist, you will have a critical role within the team working on the effective delivery of analytical programmes. You will work in collaboration with industry-leading clients, to understand the complexities of their product, interpret data and provide reliable recommendations. Responsibilities • Oversee complex analytical programmes of work relating to the analysis and characterisation of pharmaceutical and animal health products as well as Electronic Nicotine Delivery Systems (ENDS). • To co-ordinate the set-up, execution and closure of analytical projects. • Act as a primary point of contact for clients, effectively communicating to ensure expectations are fully understood and met. • Develop and validate analytical methods to ICH guidelines. • To prepare and review analytical protocols and reports. • To review, verify and interpret testing data and effectively communicate results to Clients. • Provide technical support and guidance to analytical teams as required. • May be responsible for Line Management of analytical teams. The Candidate • Graduate of Chemistry or Analytical Chemistry preferred. • Greater than five years’ laboratory experience, preferably within an industrial setting. • Experience of method development and validation of analytical methodology is required - LC-UV, LC-MS/MS, GC-FID, GC-MS. • Analytical chemistry experience working within a regulated environment would be desirable, but not essential. • Experience of dealing with Clients would be advantageous. • Experience of generating scientific documents, with emphasis on reports, is essential. • Experience of product stability would be advantageous. • Proven project management and leadership skills. • Capable of working as an individual and team player. • Good analytical and technical problem-solving skills. • Confident verbal reasoning skills with colleagues and clients. • Good IT skills. • Results driven, customer focused and commercially astute. Salary is negotiable on experience ----- Are you looking for your next challenge and advance your career in analytical development? Do you excel at problem solving and love to deliver on client expectations? Then contact Kieran Whittaker for a confidential discussion on: - Tel: 0161 923 8174 Email:

  • Analytical Manager 11/14/2017 12:00:00 AM

    Salary: £0 Location: SHEPHERDS BUSH

    Based in London, my client is a global leader in specialist imaging working towards the understanding of disease and translational drug development. You will have- Minimum of BSc in Chemistry or other relevant subject with strong evidence of your analytical expertise Extensive experience in HPLC, GC, IC (LCMS would be beneficial but not essential) Strong people management skills Evidence of leading a team Due to company progression, they are looking for an experienced and time served Analytical manager. Reporting to the head of clinical chemistry, you will be responsible for leading a multidisciplinary team of 6 specialists with in a GMP facility, in analytical chemistry and microbiology. This position requires an individual to lead by example and demands someone with strong people management, technical expertise and effective communication skills. Excellent salary £45-£50k (dependant on experience) Great career progression options.

  • Validation Specialists 11/9/2017 12:00:00 AM

    Salary: £45000 Location: OXFORD

    Validation Specialist - Biopharmaceuticals - South England - 45K This is a Permanent role- Closing date for this role is Friday 10th November My client is a fast growing biopharmaceutical company based in the South of England. Due to their continued expansion, they are currently looking to hire an experienced Validation Specialist. The ideal candidate should have significant validation experience and should have worked to GMP standards. An understanding of the Biopharma, Pharma or Medical Device sectors would be an advantage. You should have IQ OQ PQ experience. The successful candidate will join a busy validation team and will report directly to the Head of Validation. You will benefit from; + 40-45K Basic salary + Excellent Benefits Package + Great Career Opportunities. If you are an experienced Validation Specialist looking for a new opportunity please send your CV to or call 0161 923 8172 and ask for Nathan

  • GMP Biotech Production Manager 11/9/2017 12:00:00 AM

    Salary: £50000 Location: MOTHERWELL

    GMP Biotech Production Manager - Bio- Pharma Based in Scotlands central belt, my client is an innovative cell-based production company, specialising in Virology and oncology treatments. Due to continued expansion, they are actively seeking a GMP experienced Production Manager with a solution focused and positive approach. Working within a GMP environment, youll be responsible for managing a team of experienced Scientists, and promote high standards of production. Your excellent attention to detail will encourage your staff to continuously work to high standards. You will have- Minimum of BSc in life sciences subject Experience of working as a Production Manager with in a GMP facility. Experience of dealing with live vaccines or Human Cell Cultures Youll receive a highly competitive salary, an attractive benefits package, and professional development opportunities. If you have the right mix of skill, experience and attitude please email or call 0161 923 8172 and ask to speak to Nathan

  • Drug Metabolism and Pharmacokinetics and Modelling & Simulation 11/7/2017 12:00:00 AM

    Salary: £0 Location: CAMBRIDGE

    Our Client is a global, science-led biopharma company which focuses on Oncology, Metabolic and Respiratory diseases. The offer is an incredible package; the basic salary and benefits are market leading The role, Based in Cambridge, UK or Cambridge, MA is for a senior drug metabolism and pharmacokinetics professional who specialises in Modelling and Simulation as applied to oncological treatments. The Ideal candidate will have; * PHD in Drug Metabolism or related subject * Strong background in Big Pharma * Extensive publication history * Experience of leading a team within a pharmaceutical setting Your responsibilities will be; * Leading projects on understanding mode of action of new agents * Managing programmes to define compound PK properties * Scheduling strategies to deliver project efficiency * Managing drug candidates and clinical teams from pre-clinical to early-clinical studies.

  • Senior PET Radiochemist 10/17/2017 12:00:00 AM

    Salary: £0 Location: SHEPHERDS BUSH

    My client provides a world class medical imaging service to industry and academic clients. Since inception, my client has completed over 93 clinical studies and has successfully developed and-or implemented over 30 radioligands for pre-clinical and clinical use, and is in a unique position to facilitate productive, mutually beneficial relationships between academia and industry. The Role The PET team is actively engaged in an innovative and dynamic research program which includes the labelling and evaluation of novel PET ligands/tracers and assessing their application to drug discovery and development. Your responsibilities will include: • Management of assigned production laboratories, synthesis and dispensing equipment • Day to day production of new and established PET radiopharmaceuticals involving the operation of automated radiochemistry equipment and the completion of batch documentation • Writing and managing GMP documentation including, SOPS, deviations, change controls and investigation reports • Leading the development, implementation and validation of syntheses of PET radiopharmaceuticals for clinical use • Managing the introduction and validation of laboratory equipment Knowledge and Skills • Demonstrable experience in 18F and 11C radiochemistry development. Experience with other PET isotopes would be advantageous • Experience of operating and programming automated radiochemistry equipment • Demonstrable knowledge of GMP including validation, relevant regulations and guidelines • Experience in quality systems including change control, deviations and SOPs • Knowledge and experience in HPLC purification, preferably including method development • Ability to identify problems, troubleshoot and create and implement workable solutions • Ability to develop new approaches to improve or replace existing procedures or systems The Candidate • Excellent verbal and written communication skills • Excellent analytical skills and a logical approach to problem solving • The ability to work effectively as part of a team and give training and advice in their area of expertise • Excellent attention to detail • Good organisational skills and ability to work well under pressure • Knowledge of relevant legislation and regulations • Good project management skills The Benefits • Pension Scheme • Company Bonus Scheme • PMI • Life Assurance • Flexible Benefit Options Salary is negotiable on experience ---- This is an opportunity to join a world class medical imaging service Provider, able to facilitate productive, mutually beneficial relationships between academia and industry. For more information and a confidential discussion, please contact Kieran Whittaker on the below: - Tel: 0161 923 8174 Email:

  • Chief Executive Officer 9/13/2017 12:00:00 AM

    Salary: £65000 Location: NORTH WEST

    My Client are an established Pharmaceutical Food Science company, based in the North West, that specialise in the development, manufacturing and commercialisation of standardised oral food challenges to help diagnose food allergies. The oral food challenges are specially manufactured to GMP regulations and supplied to clinical trials. The company have recently secured their first major contract, and feel the time is now right for the company to be in the hands of someone who has the experience and knowledge to generate a growth strategy to guide the business onwards. This is an exciting new opportunity for someone who has a strong background in biopharmaceuticals or medical foods, product development and manufacturing. This position will be responsible for the management of all company activities including R&D, production, sales and marketing. You will be working very closely with company board of directors and stakeholders and will be expected to oversee the day to day running of the company. Salary:- £65,000+ plus excellent benefits. Location:- North West

  • QA Manager 8/4/2017 12:00:00 AM

    Salary: £0 Location: STAFFORDSHIRE

    My Client are a Biopharmaceutical Manufacturing Company in Staffordshire who specialise in the design of robust processes for their life science customers in the quality commercial, clinical and preclinical areas. They are looking for a Quality Assurance Manager that will be responsible for the day to day GMP Compliance at their manufacturing facility. This position will report to the Quality Director and will also work closely with the with the Operations and Project Management teams. Key Responsibilities Include but not limited to:- ++ Development and optimisation of the Quality Management System ++ Managing Quality System action closure ++ Being responsible for the site QA Team: coaching staff, line management etc. ++ Reviewing and approving quality documentation ++ Managing the supplier assurance and validation systems. Requirements:- ++ Previous Managerial experience ++ Relevant experience in a manufacturing or QA role ++ Possess a science degree or equivalent. Ideal candidates will have experience of biologics, though this isnt essential Salary:- £55k

  • Study Manager- E-Fate 7/31/2017 12:00:00 AM

    Salary: £0 Location: RUSHDEN

    Study Manager- E-fate- Metabolism Based in Northamptonshire my client is a fast growing CRO, providing services for the Pharmaceutical industry and they are one of the market leaders in specialist drug development Services A fantastic opportunity has opened up for a Study Manager. Main duties and responsibilities include Conduct and/or Study Direct metabolism studies for new product development based on global regulatory requirements The ideal candidate will have- Bsc in a life science subject Previous experience of conducting Metabolism/E-Fate studies in a GLP Experience of Study Directing Metabolism studies in the pharmaceutical or CRO industry is desirable Prepare study plans, amendments, file notes and deviations as required. Excellent salary (depending on experience) great benefits modern facilities. This is a rare opportunity to be involved with a successful and still growing company, that is oriented towards building long-term success for them and their employees. If you’re interested in the role contact Brian Lamont at North point today. 0161 932 8188

  • Experienced Down Stream Processing Purification Scientist, Keele (Ref:CBK0517) 5/24/2017 12:00:00 AM

    Salary: £0 Location: NEWCASTLE

    Experienced Down Stream Processing Purification Scientist - North West England My client is a Leading European Contract Manufacturer of Biopharmaceutical Products. Due to their current expansion, they are currently in the process of hiring an Experienced Microbial Fermentation Scientist. It is essential that applicants possess a strong practical experience in the purification of biomolecules, and experience of working within a GMP environment. Direct experience of plasmid DNA purification is advantageous. If successful you will benefit from; + Competitive Basic salary + Excellent Benefits Package + Great Career Opportunities. If you are an experienced Purification Scientist looking for a new opportunity please send your CV to or call 0161 923 8183 and ask for Rowan.


« previous 1 2 next »