Process Technologist

Custom Pharma Services ,
Hove, East Sussex
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Job Description

We are recruiting for a Process Technologist to join our Operations Team. Reporting into the Technical Manager in this new and varied role you will be providing support to our manufacturing and packaging operations and have an involvement with all elements of our supply chain. Operating within a solution focussed, commercial environment, you will work with a wide portfolio of OSD products, interacting with both customers and suppliers. Ideally you will have extensive production and technical experience in solid dose pharmaceutical manufacturing and practical experience of working with modern cGMP systems. About the role Working within a dynamic, friendly and supportive SME culture your focus will be to: Coordinate and implement the process validation of new and existing manufacturing processes, including technical transfers between manufacturing sites; proactively identify process and procedural improvement opportunities across production operations and manage their resolution; troubleshoot production process and technical issues whilst ensuring the highest standards of cGMP compliance are maintained and provide Technical support to the Development Team in relation to manufacturing scale-up of new formulations. Company Description About Custom Pharma Services (CPS) CPS is a full-service "Clinical to Commercial" CDMO and holds various licences to operate a range of services which includes MIA, Specials, IMP, WDL, and Vet D. CPS is an independent OSD specialist pharma contract services provider. CPS produces a range of formulation technologies including modified release and potent products such as hormones at low dose. New development and commercial manufacturing facilities for high potency contained processing have recently been acquired at a site adjacent to our existing Brighton, Moulsecoomb packaging and QC facilities. About You Qualifications, knowledge, skills & experience required: * Degree in a scientific subject and/or relevant work experience * Extensive experience and an excellent understanding of solid dose pharmaceutical manufacturing environment, equipment, processes and cGMP * Six-Sigma Green Belt and/or relevant production experience * Able to determine and execute solutions to problems with a high level of attention to detail * Competent at gathering, analysing and interpreting data * Demonstrable experience in root cause investigations and report writing * Excellent interpersonal skills with effective and persuasive communication skills * Able to work collaboratively * Able to prioritise and complete multiple tasks * Able to deliver ''right first time'' processes, with a determination to understand root cause of failures * Self-reliant & self-motivated Benefits include: Holiday; pension; health plan; life assurance; subsidised gym and annual profit related company and individual bonus payment based on successful performance. How to apply Please submit your application including a covering letter explaining how your skills and experience meet requirements of the role by Monday 15th May, 2020 Candidates should have the right to work in the UK No Agencies #INDMED

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