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Custom Pharma Services (CPS) has begun a £20 million program of investment in state-of-the-art facilities for product development and commercial supply of OSD products. The new facilities are designed to formulate and supply high potency products within a new 70,000 sq. ft. facility in Brighton, Sussex.
We are looking for a senior scientist with experience of solid-state characterisation with APIs and intermediates or material science of organic substances gained in the pharmaceutical industry in either a commercial or research & development environment. You will play a key role in developing and establishing this new area of business as well as managing the day-to-day activities of the Development Team.
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CPS is a full-service "Clinical to Commercial" CDMO and holds various licences to operate a range of services which includes MIA, MIA(IMP), MS, WDA(H), API and ManA. CPS is an independent OSD specialist pharma contract services provider. CPS produces a range of formulations including modified release and potent products such as hormones at low dose. New development and commercial manufacturing facilities for high potency contained processing are under construction at a site adjacent to our existing Brighton, Moulsecoomb packaging and QC facilities.
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In summary the role includes:
- Ensuring all development activities are established, performed and reported to meet customer, company and statutory/regulatory requirements by effective management of the Development Team.
- Identifying and prioritising Quality Control support requirements and ensuring they are executed in a timely, organised and complete manner to bring about improvement and analytical efficiency.
- Ensuring applicable quality systems are defined, established, maintained and effectively monitored to identify and close gaps (adverse trends). In order to achieve site quality objectives and meet company/statutory regulatory requirements.
- Participating in and allocating resources to ensure all analytical development/support activities are sustained and reported with ongoing activities to mitigate identified gaps or adverse trends.
- Improving the development/support group processes and adherence to customer quality requirements by applying principles of GMP.
Benefits include: Holiday, pension, life assurance, health plan, subsidised gym and annual profit related company and individual bonus payment based on successful performance.
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For details of the qualifications, knowledge, skills & experience we require and to apply please visit our website
If you would like to discuss this opportunity further please email Recruitment Manager: Jane.Austen@custompharma.co.uk
Candidates should apply by Friday 12th February.
Relocation assistance will be offered to candidates who do not live within commuting distance of Brighton & Hove
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