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QC Analyst – Pharmaceutical Analysis
My client is a pharmaceutical manufacturer based in Greater Derby area and who deliver services to regulated healthcare products worldwide. This is a permanent role for immediate hire.
As an experienced QC Analyst transitioning to QA, you will be required to work alongside a GMP laboratory environment performing technical data review of analytical data generated through routine analytical work including batch release and/or stability analysis, Raw materials.
Key Responsibilities of the QC Analyst will be:
* QC HPLC Check and Technical review and understanding of analytical testing data from - HPLC, GC, FTIR and wet chemistry in accordance with current BP/EP/USP
* Covering a range of processes - Raw materials, Batch release and stability testing
* Supporting and write up CofA within GMP guidelines
* Follow SOP’s within quality management system
* Delivery and Investigate and deliver OOS, CAPA and deviations from the analytical laboratory
The successful candidate for the QC Analyst role must have:
* Chemistry or related science degree plus 3 years of relevant laboratory experience, ideally in a GMP or UKAS environment
* Experienced at using HPLC or GC in a GMP industrial environment
* IT proficient, a good communicator and looking to move from lab to QA
* Excellent attention to detail and be able to prioritise work to specified deadlines.
* Flexible approach to working
If you are an experienced QC Technician, Analytical chemist, QC Analyst or a stability Analyst with industrial experience in a GMP environment looking for a new challenge moving toward QA then please apply now!
About us: Templarfox if a privately owned recruitment business leading in executive search, management selection, Salary benchmarking and Business development services. The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK and on this occasion TemplarFox Consultancy is acting as an employment agency