Part Time Microbiologist (2 or 3 days a week)Gloucestershire £17,750 to 20,000 Per Annum pro rata My client is a premier food and...
QA Manager - Pharmaceutical Development & Manufacturing
Based in London
Salary c£60,000 + Bonus + Excellent Benefits
Do you have extensive auditing experience within GMP or GCP environments?
Would you like to work for a successful and growing Pharmaceutical company?
My client are a specialist pharmaceutical company, with a strong development pipeline; due to continued growth they are looking to hire a QA Manager to take a lead role in the companies auditing schedule. You will act as a deputy to the Head of Quality, ensuring GMP and GCP regulations are met during the drug development cycle, including IMP manufacture, clinical trials (Phase I to III), product development, formulation, analytical and commercial manufacturing. The company has a development portfolio of both small molecule and biological assets.
This role has no direct reports but may grow into a line management role as the department grows.
Specific responsibilities will include;
- Planning, conduct, reporting and follow up of audits in accordance with the annual schedule (internal and vendor audits)
- Providing input to the audit schedule
- Independent QA review of key quality documents and deliverables eg protocols, CSRs, QTAs, SOPs
- Providing process development support to operational groups
- Supporting identification and implementation of CAPAs
- Management of Training and Training Records
- Providing in house training and general QA support
To be considered for the role you will need extensive auditing experience, leading both internal and external audits, ensuring GxP compliance. The role would suit someone who has either GMP or GCP experience, and offers the opportunity for someone to grow into either of these areas. You'll need experience of CAPA Management and SOP Management, with previous experience of regulatory inspections.
This role would suit someone who is an excellent communicator, and likes a collaborative and interactive working environment. This is an excellent opportunity to join a forward thinking and growing pharmaceutical company.
Key Words "QA Manager, Quality Assurance Manager, Lead Auditor, GCP, GMP, Clinical Trials, Pharmaceutical Development, GxP, IMP Manufacture, QC, Pharmaceutical Product Development, formulation, CAPA, SOP"For more information and to apply, please call Neil Walton on 02030964706 or apply online.
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.