Jobs

We found 91 job(s) for you:

  • Technical Quality Director

    Salary: £0 Location: MOLESEY

    Technical Quality Director- Pharmaceuticals Based in the Southern UK, My Client is a specials, Unlicensed Medicine, Manufacturing company. A rare and fantastic opportunity has risen for an experienced, technical Quality Director, to join and lead the company in its Quality management. You will be responsible for leading the company in all quality activities, including strategic development, governance and compliance such as MHRA, GMP/ GxP. You will also be responsible for helping to drive continued business growth and promoting a candidate positive approach. You will have- BSc (of higher) in Pharmaceutical sciences or other relevant subject. 10 years plus industry experience in a senior position Extensive Quality management experience with in a MHRA & GMP/ GxP environment Knowledge of Specials/ Unlicensed products RP experience (preferred) Salary- Fantastic salary (depending on experience and to be discussed verbally, at point of application) Excellent benefits

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  • R&D Cosmetic Chemist

    Salary: £35000 Location: GWENT

    R&D Cosmetic Chemist- South Wales- Cosmetics- up to £35k Based in South Wales my client is a world class, private label cosmetic company specialising in cosmetics aerosols. They have a brand new, purpose-built, R&D facility and are looking to take on a formulations chemist with at least 3 years industry experience (cosmetic or personal care). The successful candidate will be a mature, level headed person with a strong work ethic and has the ability to work on both an independent, self-sustained or team focused environment. You will have- BSc or higher in a science related subject 3 years plus experience in formulations for the cosmetic/ personal care sector Salary- £25-£35,000 dependant on experience Fantastic training and development oppurtunities

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  • PI Buyer

    Salary: £0 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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  • Quality Control and Analytical Chemistry Manager

    Salary: £0 Location: SHEPHERDS BUSH

    The Client My client, based in London, is a global leader in specialist imaging working towards the understanding of disease and translational drug development. The Role Due to company progression, they are looking for an experienced and time served Analytical manager. Responsibilities 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. • Managing and leading a multidisciplinary team of highly specialist PET analytical chemists, microbiologist and lab technicians, and ensure they are fully trained and competent for their roles • Managing the daily activities in the QC laboratories for the delivery of PET products to support clinical demands • Releasing PET radiopharmaceuticals for human use • Leading analytical method development for implementation of all new PET radiopharmaceuticals for human use • Overseeing management of Raw Materials entering the manufacture of clinical batches of radiopharmaceuticals • Overseeing the environmental monitoring program, in conjunction with the microbiologists. • Identifying and implementing opportunities for continuous improvement in the QC laboratories. • Ensuring the QC laboratories, equipment and analytical methods are fully functioning and compliant and conform to company standards and the appropriate regulatory standards in the UK The Candidate • Minimum BSc. Degree in Analytical Chemistry • Operational expertise of laboratory equipment • Knowledge of relevant legislation and regulations • Strong people management skills • Good project management skills • Demonstrated ability to work in a multidisciplinary team and to assimilate a working knowledge of areas outside of their core competency. • QP qualification (desirable) Salary is negotiable on experience

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  • Regulatory Affairs Manager

    Salary: £0 Location: LONDON

    My Client are a leading Cell and Gene Therapy company looking to attract a Regulatory Affairs Manager for a 9 month FTC. With offices across the UK and a translational therapeutics pipeline secured over the next 5 years, this is a great position for someone looking to gain managerial experience within a world class environment. Responsibilities: To support the development programmes in place, providing expert advice to ensure the programmes are developed in a way which meet regulatory requirements; To provide expertise in CMC requirements of product and process development To implement optimal regulatory strategies for each programme in agreement with the Head of Regulatory Affairs, Knowledge of advanced therapy clinical trial applications and GMM submissions to support gene therapy clinical trial applications

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  • Post Doc - Upstream Scientist

    Salary: £0 Location: CAMBRIDGE

    Upstream Process Scientist - Cambridgeshire - £20k-£35k My client is an innovative biotech firm looking at new antibiotic technologies. They are expanding their teams and are looking for an Upstream Process Scientist. Youll be responsible for upstream development in flasks and bioreactors, scale-up activities, QC analysis and impurity monitoring. Youll be responsible for analysing and reporting on all studies. There will also be the opportunity for European travel with work. Youll need a BSc / MSc or PhD in relevant life sciences. You should have experience in microbiology, aseptic processing, good maths skills, and ideally experience in bacterial fermentation and / or bacteriophage.

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  • Clinical Immunologist - PRO-DEV-CLIN

    Salary: £0 Location: MOTHERWELL

    The Client My clients mission is to develop and commercialise innovative cell-based products to treat disease, improving patient health and Quality of Life. A clinical development company based in Scotland, with a cell-based product pipeline capable of treating a variety of disorders including cancer and severe viral infections. My client is currently conducting Phase II/III clinical studies of its lead product, in renal cell cancinoma, non-small cell lung cancer and melanoma patients. The Role If you are passionate about cancer immunotherapy and are looking to work within a challenging, dynamic, and rewarding environment, then this company represents an excellent career move. This is an opportunity to be part of a growing, ambitious business where people development is critical to future success. As they continue to expand, there will be career opportunities on a global scale. My client is an emerging cancer immunotherapy company developing cell-based treatments for cancer and severe viral infections. Based in the central belt of Scotland, the successful candidates will form an integral part of my clients rapidly expanding Product Development team, which is responsible for delivering the preclinical portfolio of ?d T cell-based therapies. Responsibilities The Senior Scientists and Scientists in Clinical Immunology will work within the Product Development team and, providing specialist knowledge and experience of working with patient-derived samples, will apply their expertise to the design, implementation and completion of projects crucial to the CAR-T and allogeneic pipelines. In particular, the post-holder will contribute/lead in developing and transferring methods for successful expansion, transduction and assays of patient-derived material, especially in the ImmuniCAR project. However, the successful candidate will also be expected to become actively involved across the range of pipeline products to aid the Product Development team in achieving their aims. To successfully achieve the project objectives, the post-holder will be expected to apply expertise across a number of practical skills, including primary cell culture (isolation, expansion and assay development), flow cytometry and cryopreservation of cell banks. Other responsibilities will include support of other departments, the training and supervision of junior team members and contribution to general lab maintenance compliant with GMP procedures. • Perform cell isolation from both healthy donors and patient-derived materials • Optimize methods for the isolation, expansion, transduction and differentiation of specific subsets of PBMCs from patients with a range of indications • Undertake cell culture of primary immune cells, cancer cells and immortalised cell lines and perform functional cell-based assays such as cytotoxicity and proliferation assays. • Design and perform multiparameter flow cytometry experiments • Develop SOPs for the use of patient or donor-derived material for clinical applications • Devise assays to Quality Control the final cell therapy product and liaise to transfer release assays to other departments • Work both independently and with the team to analyse data generated from experiments, draw appropriate conclusions and decide upon next steps. • Maintain documentation to appropriate quality standards, including, but not limited to, laboratory notebooks, standard operating procedures, COSHH/BIOCOSHH assessments and Risk Assessments. • Carry out literature reviews and collate information to identify information useful for the development of novel assays or the improvement of current processes and, where appropriate, to prepare applications to protect intellectual property The Candidate • Have significant experience working in research or biomedical laboratories, ideally holding an advanced degree (PhD or Masters) in a relevant subject • Have extensive knowledge of cell therapy and, ideally, proven experience gained in an industrial setting. • Be experienced in working with patient and healthy human donor material across a range of applications, including cell culture, cell-based assays, and flow cytometry, as appropriate to the role. • Be familiar with GxP procedures, ideally in a cell therapy context. • Have experience in controlled document preparation • Have a keen interest in cell-based therapies and their application to treat cancer and viral/bacterial infections. • Have excellent team working and communication skills Salary is negotiable on experience

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  • Senior Immunologist (TL)

    Salary: £0 Location: ABERDEEN

    Immunology Team Leader - Scotland My client are a pharmaceutical company focused on developing therapeutics from live bacterial culture. Due to significant expansion in their commercial and R & D operations, there is a need for a Team Leader in Immunology to start within the next 3 months. If you are an experienced Immunologist focused on working with live biotherapeutic products and have experience of line management, then this could be a great role for someone who is looking for a change of pace! Requirements for the role include; + PhD with relevant post-doctoral or industry experience [>3-4 years] + Experience of In Vivo or In Vitro immunology techniques + Expertise in immunological assay development + Home Office license preferable. If this sounds like you, please do not hesitate to get in touch.

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  • Full Stack Developer

    Salary: £0 Location: LONDON

    The Client My client, based in Covent Garden, is a market leader providing a platform to collect Music Royalties for Television, Radio and the Internet. Utilising a wide range of technologies from Web Tools, noSQL, Relational Databases, Pattern Recognition engines and distributed data services, they support a number of customers including, Virgin, Fox & Channel 4, providing excellent cost saving solutions for managing Music Royalties. The Role My client has a requirement for a high calibre Full-Stack Developer. This is an incredible opportunity to join a diverse team of professionals, designing, implementing and deploying complex, performance-critical software systems. The Candidate This is a diverse and energetic team, you will be creative and have an inquisitive mind, capable of contributing to a larger team project and working to strict deadlines. You will have experience in Full-Stack technologies such as C#, React.js, SQL, JavaScript and jQuery. Salary is negotiable on experience ---- This is an opportunity to join an industry leading company working with FTSE companies. For more information and a confidential discussion, please contact Kieran Whittaker on the below: - Tel: 0161 923 8174 Email: Kieran.Whittaker@wearenorthpoint.com

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  • GCMS Technician

    Salary: £25000 Location: WOKINGHAM

    GC MS Analyst- Berkshire- Permanent- up to £25,000 Based in in Berkshire, my client is a world leader in the chemicals and coatings sector with a growing international presence. They are currently looking to appoint a GC MS analyst to join the QC Testing team, who will be tasked with the day to day running of the companies GCMS, to ensure their raw and finished goods are within defined quality limits and are fit for purpose. You will have- • A Degree in Chemistry or related scientific field • 1 to 5 years of experience in chemical manufacturing industry (Please note this must be a chemical industry. Pharma/ food would not be suited for this role) • GCMS experience Excellent facilities Great salary- up to £25,000 (dependant on experience)

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