Pharmaceuticals

  • 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.

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  • 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.

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  • PI Buyer 5/14/2018 12:00:00 AM

    Salary: £25000 Location: SLOUGH

    My client, based in Berkshire, has established themselves as a leading distributor in Japanese market and supply to currently to 13,000 customers. After careful consideration they have now decided to join the UK Market and expand their portfolio of clients. They are committed to supplying Pharmacies, Doctors, Hospitals and Wholesalers with the Highest Quality Branded and Generic Pharmaceutical products at the most competitive prices, together with a comprehensive range of ancillary products. Dedicated to the principles of best practice and high quality in all its activities, particularly in supply and service to its customers, for my client it will always be a pleasure to deal with their customers. My client is committed to support and development of staff, Systems and Working Relationships as this will lead to great work, enthusiasm and loyalty which is the key to achieving its primary mission. Due to this continued ambition, my client now seeks to hire an experienced PI Buyer. Responsibilities • Supporting Purchase of pharmaceutical products from EU countries. • Maintain a database of information relating to potential new products. • Maintain records of stock usage through sales to ensure price lists are correct and up to date. • Obtain information on potential new products and locate the cheapest sources. • Work cooperatively and effectively with the Regulatory affairs department on all issues associated with licensing products. • Entering Purchase order to the system and ensure invoice are sent in a timely manner for contract labelling. • Opening products codes in the system. • Preparing offers lists to suppliers. • Report to related parties with purchase of products that need attention (control drugs, temperature control products) and liaise with warehouse to store correctly. • Arrange shipment and make sure the goods to be delivered in a timely manner. • Monitoring and keeping records of shipment schedule (ETD and ETA). • Liaise with carriers and negotiate on rates. • Calculating profit margin of Purchase order and Blanket order. • Create various purchase reports and analyse purchase cost and profit. • Checking and matching purchase invoices against purchase orders. • Liaise with finance team, warehouse and production to handle with damage/shortage goods from supplier and take a necessary action. • Liaise with finance team to update purchase record. • Check stock levels. • Filing documents. • Other ad hoc task The Candidate • Graduate Qualification. • Able to use Microsoft Excel to a good standard. • Able to use Microsoft Word to a good standard. • High level of communication. • Able to work without supervision. Salary is negotiable on experience

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  • Regulatory Affairs Director 5/14/2018 12:00:00 AM

    Salary: £90000 Location: CAMBRIDGE

    Director, Regulatory Affairs- Biotechnology- Cambridge- ExcellentSalary Based in Cambridge, my client is a market leader in human anti-body development for the immuno-oncology, inflammation, haematology and infectious disease sectors. Due to business development, they are currently looking for an experience Director of Regulatory Affairs with Significant industry/biotech experience of early-phase clinical trials You will be responsible for providing strategic guidance for the business in the development of new antibodies and to lead the company in all matters relating to regulatory affairs. Minimum of BSc in appropriate scientific field Significant industry/biotech experience of early-phase clinical trials Expert level of knowledge in regulatory affairs Knowledge of Development Good Practices (GxP) Excellent salary- to be discussed at application Great benefits

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  • Quality Compliance Manager 5/14/2018 12:00:00 AM

    Salary: £45000 Location: CAMBRIDGE

    The Client My client provides proprietary technologies and complementary services to organisations involved in the development of biopharmaceutical products. Working with companies and academic groups all over the world, including most of the top 20 biopharmaceutical companies, my client supports the development and manufacture of better treatments for patients The Role To lead and manage the Company’s Quality Management system and ensure that the Company is compliant with legislative and regulatory requirements in respect of scientific work undertaken. To develop and maintain a Quality Management System (QMS) to ensure that the company complies with legislative and regulatory requirements and best practices, particularly with respect to the use, storage and disposal of: - • Human tissues • Radioactive materials • Genetically modified organisms (GMO) • Other hazardous materials, including toxins and cytotoxic compounds Responsibilities • To oversee the application and/or maintenance of the Human Tissue Act (HTA) licence, Research Ethics Committee (REC) approvals (for the use of human tissues) and notifications under the GMO and radioactive waste regulations • To monitor the legislation and regulations applicable to the company’s scientific activities and implement any changes required to ensure that the company remains in compliance • To develop and maintain a Company database of COSHH forms and Risk Assessments and ensure staff are aware and adhering to them • To develop and maintain a database of Material Safety Data Sheets (MSDS) and ensure that a MSDS is available for all materials that are being used • To develop, implement and manage the Company’s scientific document retention policy • To develop a plan for implementing ISO9000 compliance in Cell Line Development • To develop and implement a plan to allow GMP compliant sub-contracting within the Group companies including any GMP analytical services carried out in Cambridge • To develop and maintain the UK Company’s QMS and where appropriate ensure this is aligned with US groups • To lead the development and implementation of new SOPs and ongoing review, revision and replacement of SOPs • To identify and develop ways to improve quality across the Company and ensure best practice is adopted throughout the organisation • To conduct regular internal audits for compliance with the legislation, regulations and the QMS and ensure that corrective and preventative actions (CAPA) are implemented and provide a written report of such audits and the CAPA to the Board Audit & Compliance Committee • To ensure that external audits under scope of this role, including by regulatory agencies, are prepared for • To undertake any other duties relevant to the position and level • To effectively manage one or more teams and, through the performance management system, provide guidance and support associated with both their technical and personal development • To foster relationships with key internal and external stakeholders and partners to support proactive compliance with legislation and regulations and the Company’s QMS • To take the lead in providing training to staff to ensure that they are aware of the legislation, regulations and best practices that affect their work and what they need to do to comply with them • To be a member of the HTA Governance Committee The Candidate • Experience of working in a regulated environment • Familiarity with Quality Systems including EU GMP • Experience of developing and/or maintaining a QMS and of conducting audits • Excellent interpersonal skills, including tact and the ability to foster good relationships • Planning and Organisation • Able to effectively plan and organise own work load and that of small teams of reports • Communication • Excellent communication skills, including the ability to write clearly and unambiguously to Regulatory standard • Focused to achieve results • Critical and intelligent attention to detail and high standard of accuracy in own work • Desirable Skills & Qualifications • A higher degree within the Life Sciences • Understanding of scientific research • Working experience of the Human Tissue Act • Experience of working within a GMP regulated environment Salary is negotiable on experience

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  • Assay Biologist 5/14/2018 12:00:00 AM

    Salary: £40000 Location: CAMBRIDGE

    Assay Biologist My client are looking for an experienced Assay Biologist. +Develop screening assays for drug targets using appropriate assay formats, to support the drug discovery process from hit identification to lead optimisation +Biochemically characterise compounds to develop an in depth understanding of their mechanism of inhibition +Explore and implement novel assay technologies for use within the group +Interact with other key members of multidisciplinary teams including chemistry, biophysics and protein production group Youll need- *PhD in Enzymology/Protein Biochemistry *Proven post-doctoral experience *Proficiency in assay development If you would like to be considered for this role, please send your CV to adam.robinson@northpointrecruitment.com or call on 01619238186.

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  • 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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  • X-Ray Software Developer and Crystallographer 5/14/2018 12:00:00 AM

    Salary: £55000 Location: CAMBRIDGE

    X-Ray Software Developer and Crystallographer - Cambridgeshire - £55k + Assistant Director level + Excellent salary and benefits package + Software development / coding My client is a global leader in drug discovery and development for oncology. They now seek an expert-level X-Ray Software Developer and Crystallographer to join their molecular sciences department. Youll have a PhD and substantial industrial experience in macromolecular crystallography as well as writing code in web-based programming languages. The benefits will include a fantastic package and career development opportunities at a highly successful Pharmaceutical company: + Salaries from £55,000 (flexible depending on experience) + Full benefits package

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  • Shift Engineer 5/14/2018 12:00:00 AM

    Salary: £34000 Location: ROMFORD

    Shift Engineer - Pharmaceuticals - London - 34K + Shift Allowance My client is a leading specials manufacturer based in the South of England. Due to their continued expansion they are currently looking to hire an experienced Shift Engineer. The ideal candidate should have a strong background working within the pharmaceutical sector. You must have a background working in an engineering discapline. A strong understanding of GMP standards is essential. You must have worked with PLCs and have a strong working knowledge of building services including HVAC. Experience writing SOPs would also be an advantage. The successful candidate will join a busy engineering team on a shift basis. You will benefit from; + 30-35K basic salary + Excellent Benefits Package + Great Career Opportunities

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  • Assay Biologist 5/14/2018 12:00:00 AM

    Salary: £40000 Location: CAMBRIDGE

    Assay Biologist - Cambridgeshire + Screening assays for drug discovery + Biochemical assay development + Great perm role with benefits My client is a global leader in drug discovery and development for oncology. They are looking for new Assay Biologist to join their teams for assay screening on small molecules. Youll be responsible for developing biochemical screening assays for drug targets and exploring new assay technologies. You will need a PhD and relevant experience in protein biochemistry / enzymology. The benefits will include a fantastic package and career development opportunities at a highly successful Pharmaceutical company.

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