• QA Compliance Officer - Audit 7/30/2018 12:00:00 AM

    Salary: £0 Location: Salisbury

    The Client My client is a fast-growing biopharmaceuticals company based in the South-West of England. Experts in developmental production and the bringing to market of biologicals, my client have decades of experience in production, characterisation, process and analytical validation of life saving biopharmaceuticals, including the Anthrax Vaccine. The Role Taking on the mantle of QA Compliance Officer - Audit You will be charged with formulating proposals for and provide active management of operational projects with responsibility for ensuring all aspects of project delivery for both the company and its customers. Responsibilities • To organise, plan and perform internal and external (supplier) audits, to follow up open audit reports and conduct reviews of audit responses in order to close out audit reports • To ensure supplier questionnaires are satisfactorily completed by key manufacturers and suppliers in a timely fashion. • To liaise with suppliers to obtain relevant information for their approval to provide key materials and services (incl. processing, BSE/TSE) • To approve GMP Monographs to ensure that suppliers are appropriately approved and BSE/TSE certificates are satisfactory. • To produce Quality Technical Agreements for the supply of and services from critical suppliers • To initiate and progress Supplier Complaints to closure. • To update the supplier monitoring database and associated spread sheets used for tracking. • To assist with the QA overview of manufacturing and testing areas. • To provide KPI reports measuring the performance of the systems and the team. • To undertake relevant training. • To undertake work in accordance with the Health and Safety policies and procedures and to work within any Quality Systems that are applicable to the site. • To comply with policies and procedures ----- Are you prepared to begin a new chapter in your career? If so, this could be the role for you! For more information and a confidential discussion, please contact Kieran Whittaker on: - Tel: - 0161 923 8174 Email: - Salary is negotiable on experience

  • Programme Scientist 7/25/2018 12:00:00 AM

    Salary: £40000 Location: Aberdeen

    My client is a leading pharmaceutical company focusing on developing live biotherapeutic products from the human gut microbiome. So far, my client has two clinical stage programmes in IBS and IBD as well as a strong pipeline of pre-clinical programmes in autoimmunity, inflammation, oncology and CNS disease. Due to recent expansion, my client is looking for a programme scientist to help provide subject matter expertise to help bridge the gap between pre-clinical to regulatory by providing scientific support to the manufacturing, clinical and regulatory teams. Report writing, and presentation skills play a key part with this role as there will be meetings held with numerous stakeholders related to the business. Experience / Qualifications Required • Bachelor’s degree in microbiology, biological sciences or related discipline • At least 2 years’ experience working in biological sciences or on microbiome derived products • Expertise in scientific programmes from preclinical to product development • Excellent report writing skills • Excellent communication skills and ability to work well within a team Key Areas of Responsibility • Provide scientific support to the manufacturing, clinical and regulatory teams, bridging the gap between pre-clinical to regulatory in providing scientific knowledge of the product; • Understand the needs of regulatory, clinical, manufacturing and research regarding candidate strains to co-ordinate activities between the departments; • Support the drafting of regulatory documents with scientific input pertaining to the candidate strain(s) such as Investigator’s Brochure and IMPD with the team; • Provide scientific knowledge regarding the candidate strain(s) at key meetings, Scientific Advice meetings with the regulators, meetings with clinical CRO’s, clinical Site Initiation Visits; • Provide scientific expertise in product development activities, such as antibiotic resistance testing, media, bacteria specific knowledge, preclinical studies; • Collection, analysis and presentation of scientific information pertaining to the products;

  • Senior Lead Formulation Scientist 7/19/2018 12:00:00 AM

    Salary: £40000 Location: Nottingham

    My client is a contract development and manufacturing organisation (CDMO) specialising in advanced characterisation, Intellectual Property consulting, formulation development, analytical services and clinical manufacturing. Due to continued expansion they are looking for a Senior Lead Formulation Scientist to join a diverse and dynamic team, in a fast-paced environment, providing technical excellence in the development of solid-oral/topical based dosage formats. You will need to demonstrate an in-depth knowledge of techniques, instrumentation and interpretation of scientific data within cGMP guidelines, as well as coaching and mentoring junior staff. You will need: BSc in Pharmaceutical sciences, Chemistry or another relevant subject. GMP Industry experience is a must Experience in formulating a range of Pharmaceutical dosage forms, in particular solid oral dose forms. Experienced in using a range of Pharmaceutical Processing equipment, in particular wet and dry granulation, spray drying, tabletting and coating. Salary- Up to £40,000 depending on experience Fantastic career oppurtunities • Contributory Pension scheme • 25 days holiday - plus bank holidays • Death in service • Healthcare provision • Health Shield • Free parking • Childcare vouchers • Perk Box • Learning & Development opportunities

  • Technical Leader 7/12/2018 12:00:00 AM

    Salary: £32000 Location: Bradford

    My client is a multinational business with laboratories throughout 9 locations within the UK focusing on Pharmaceutical, Biotechnology, Food, Environmental, Agrochemical, Petrochemical and Chemical sectors. They are a science led business focused on delivering expertise and capabilities in which their clients demand within the above sectors. Due to expansion, there is an urgent need for a Technical Lead with experience in Analytical and Pre-Formulation Sciences. Role: Technical Leader Base: Bradford Qualifications/Role Requirements: + PhD in related Discipline + Small Molecule and Drug Development experience + Experience with Drug solubility + API solid form optimisation + Salt / polymorph / crystallisation / excipient compatibility screening + Familiarity with the drug development regulatory pathway (e.g. IND, CMC requirements). In addition 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. 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. If you are looking for a new position and would like to know more, please do get in touch with Robert Frame on 0161 923 8189

  • Antibody Engineer 6/19/2018 12:00:00 AM

    Salary: £0 Location: Cambridge

    The Company My client is a world leader in Immuno-therapies, and prides itself in utilising the bodies’ own immune system to fight cancer. It does this through the combinations of antibody based, vaccine and cell therapies. Based in a newly opened site in the heart of Cambridge, this is an exciting opportunity to join the Discovery Technology Group for the development of antibody based therapeutics. Will you join them and contribute to this exciting journey? The Role This group is primarily focused on bringing in new technologies and platforms into the company worldwide. They are looking for a highly motivated and enthusiastic scientist to join a motivated group. Key Responsibilities • Expected to work independently on technology development and to report to the technology group. • Able to design experiments and is highly motivated • Able to present on data and to integrate new technologies throughout the company • Give regular presentations to the companies UK group, and beyond via laboratory meetings and journal clubs • Laboratory based – is willing to take the lead within the laboratory and serve as subject matter expert Salary is negotiable on experience ----- Are you ready for the next chapter in your career? For more information and a confidential discussion, please contact Kieran Whittaker on: - Tel: - 0161 923 8174 Email: -

  • QMS and Compliance Lead 6/5/2018 12:00:00 AM

    Salary: £0 Location: SALISBURY

    Focused on curing the worlds deadliest diseases, this pioneering biopharma is now seeking a QMS and Compliance Lead to join their team on a fixed term basis. Acting as QMS and Compliance Lead will see you at the helm of a Cross Disciplined team, delivering compliant Quality Systems and developing an industry leading QMS. Other duties include: • To keep up to date with the requirements of the Medicines Authorities across the EU and rest of world (where relevant) • Provide oversight and direction to development and GCP teams to enable new products to be brought to market. • To provide input and leadership with the Quality Management System (QMS) within the business to drive simple compliant systems. • Assistance with regulatory inspections and client audits. • To promote and uphold the highest standards of professionalism in order to create, maintain and enhance the reputation of the business, amongst its customers and stakeholders both nationally and internationally • To review company Project Files (PSFs, commercial project files etc) to ensure compliance with the current regulatory requirements and company procedures. • To deliver continuous improvement in all areas of the business to enhance the quality, delivery, rate of growth and competitiveness • To liaise and interact positively with appropriate regulatory authorities to ensure company compliance This is a fantastic opportunity and an opportunity to join a team where you can be proud to be producing life-saving products that really make a difference. The company boasts flexible working hours, innovative projects and an incomparably intelligent team to work alongside.

  • QC Senior Technologist 6/5/2018 12:00:00 AM

    Salary: £34000 Location: Salisbury

    My client is a fast-growing biopharmaceuticals company based in the South-West of England. Experts in developmental production and the bringing to market of biologicals, my client have decades of experience in production, characterisation, process and analytical validation of life saving biopharmaceuticals, including the Anthrax Vaccine. Taking on the mantle of QC Senior technologist will see you reporting directly to the QC Analytical Manager. You will be tasked to manage and perform the transfer/validation of analytical methods from Development into a GMP environment in QC Analytical Services (QCAS). The role involves all activities involved in transferring analytical methods from Development to QCAS, including running analytical methods in both Development and QCAS, writing transfer/validation protocols, executing protocols in the laboratory, writing up the associated transfer/validation reports, performing release analysis and training existing members of staff in transferred methods. Are you prepared to begin a new chapter in your career? If so, this could be the role for you.

  • PI Sales Manager 5/23/2018 12:00:00 AM

    Salary: £40000 Location: Slough

    Based in Slough, my client is a global pharmaceutical company looking to take on an experienced, and driven PI Sales Manager, to join and lead a dynamic and diverse team. You will be responsible for business growth and the profitability for Parallel Imports within a Pharma wholesale business, building effective relationship with existing clients as well as bringing on board with new clients to secure the long-term growth and managing the commercial department to improve productivity. You will have: • Experience working in and selling Parallel imports in the pharmaceuticals sector • Relationship Management Skills with Suppliers and Clients • Budget Management • Strong interpersonal and negotiation skill • Knowledge of Commercial agreements • Reporting Skills relating to Sales, Profit, Customers and Suppliers Salary is dependent on experience but expected to be around 40k.

  • Experienced Downstream Processing Purification Scientist 5/23/2018 12:00:00 AM

    Salary: £26000 Location: Staffordshire

    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. Salaries for the position are expected to be in the 24-26k range.

  • Group Leader Biophysical Sciences 5/14/2018 12:00:00 AM

    Salary: £70000 Location: CAMBRIDGE

    Group Leader - Biophysical Scientist - Cambridgeshire - up to £75k + SPR for protein / small molecule + NMR, MS ITC + Excellent salary and benefits package My client is a global leader in drug discovery and development for oncology. They are looking for a Group Leader in Biophysical Scientist to join their Molecular Sciences deparment - an established group of interdisciplinary scientists in Biophysics. You should have a minimum of 10 years drug discovery in industry or academia including: + Line/Project management experience + SPR for proteins / small molecule + ITC, NMR, MS, Protein expression + Ability to defend a scientific viewpoint welcomed! The benefits will include a fantastic package and career development opportunities at a highly successful Pharmaceutical company: + Salaries between £55k-75k (flexible on experience) + Market Leading benefits package


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