Description
An exciting opportunity has arisen for an experienced Manager in Quality Control to join a successful and growing Pharmaceutical team in West London. Our clients have a strong corporal backing, as they are world leaders in the pharmaceutical industry however; this particular role has a small company feel. Working as part of a small team of 10 the manager will help to implement, maintain, and assist in the development of the Quality Management System (QMS).The role of the Manager Quality Control is to perform IPC, stability and Quality Control batch release testing to SOP under cGMP
Salary- £40.000
Pension Up to 9%
25 days holiday
Bonus 9%
Stock units which can be sold after 2 years and topped up annually
Key Responsibilities:
- Perform the following established Quality Control test methods including, but not limited to ELISA, plaque assay, gel electrophoresis, spectroscopy, PCR, and chromatography to support batch release and stability studies
- Write/revise/review SOPs, risk assessments, COSSH forms, protocols and reports in terms of providing technical input.
- Interact with Quality Assurance to ensure Quality Control batch release / stability
- Schedule and Supervise the Quality Control testing performed by Associate and Senior Associate Quality Control staff.
- Execute and reinforce good documentation practice in accordance with cGMP.
- Manage / perform equipment validation, assay validation
- Testing and related documentation are all completed in accordance with cGMP.
- Train other members of the group on Quality Control assays within the scope of experience and knowledge.
- Raise change controls, non-conformance's, and CAPAs related to Quality Control and perform non-conformance investigations.
- Review Quality Control test data to ensure compliance with good documentation practice.
- Testing and related documentation are all completed in accordance with cGMP.
- Application of technical and scientific experience in the research and development of techniques and assays to further characterize products.
- Additional responsibilities / tasks may be assigned
Job Requirements:
- BSc or MSc biochemistry or other related biological science.
- Demonstrated extensive experience working in a commercial GMP environment in a lead Quality Control role
- Substantial GLP / GMP experience in a relevant work environment.
- Computer literacy (including MS Word and Excel.
- Ability to work well in a team.
- Effective communication skills.
- Good organizational skills.
- Supervisory experience.
To apply for this role please send a copy of your CV to Layi Shonubi or call