We are currently looking for a QA Manager with extensive knowledge of GLP to join a Research company based in London, UK.
As QA Manager, you will be expected to develop a QA GLP & GCP laboratory audit strategy and implement an audit program in line with the overall QA strategy. You will also be expected to provide assurance that company GLP & GCP laboratory studies are performed in accordance with GLP regulatory requirements and local laws.
Day to day, responsibilities of this QA Manager will include:
- The authoring of QA SOP’s and review of functional SOPs
- The implementation of in-house GLP training programmes
- The implementation and management of audit programs including audits of Study Reports, Facilities, In Process, Critical Phase, Protocols, Sub-Contractors and Suppliers and signing QA statement on GLP reports and protocols audited.
Project management responsibilities of this QA Manager position will involve providing support to pre-clinical staff and study directors on quality/regulatory issues, providing GLP& GCP laboratory advice and support to pre-Clinical personnel and ensuring project timelines are met.
The ideal candidate for this QA Manager role will hold a Degree, Masters or PhD in a Scientific Discipline (or equivalent) and will have industry GLP regulatory pharmaceutical/CRO experience. As you will be ensuring work is carried out according to GLP & GCP standards and you will be providing guidance and information on all aspects of Quality Assurance related to GLP activities, it is essential that you have experience of QA hands on auditing and Quality System experience including protocol, report, in process, critical phase and suppliers. A good knowledge of pre-clinical processes is also required.
For more information, or to apply for this QA Manager position please contact Jason Johal at CK Science on 01438 723 500 or email firstname.lastname@example.org. Please quote reference ST20673 in all correspondence.
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