GMP Officer

I am recruiting on a permanent basis for a Documentation GMP Quality Officer to work within a regulated pharmaceutical environment. This opportunity is a permanent position for immediate start.

You will be responsible for documentation GMP Quality Officer within Microbiology and chemistry data:

• Review laboratory data for batch release, analytical and/or microbiology
• Prepare customer test/technical protocols and reports
• Support Investigation & resolution of deviations to support and allow batch release
• Support, recommend, and monitor corrective and preventive actions (CAPA)
• Documentation, Raw material review, and data integrity
• Write documentation supporting for Batch release, SOPs

• Will have a degree or equivalent qualification in a science-based subject
• Ideally GMP documentation experience in Pharmaceutical, Biotechnology, food, or medical device
• Ideally a minimum of 2 years pharmaceutical experience within Quality Assurance/documentation
• Attention to detail as training will be provided

Key Words: QA, Quality Risk Management, Quality Systems, Supplier Management, Audits, CAPA, Quality Assurance, QMS

If you believe you hold the relevant background experience and looking for a new role as a Documentation GMP Quality Officer within a successful and growing business, then this is the role for you.

Please note the client cannot accept applications from candidates who are not based in the UK or who require visa sponsorship.

About us: Templarfox is 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.

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