Job Description
Northreach is a dynamic talent solutions specialist that connects businesses with top talent in the cell & gene therapy, fintech, and digital sectors. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that encourages equality, innovation, and professional growth.
Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below.
I am working with a Clinical stage biotech company that are pioneering the development of regenerative medicines. There is a pipeline of several ATMPs that are at the forefront of clinical medicine for ocular diseases. They are looking for a QA Manager, you will be responsible for providing QA Support to manufacturing operations.
Are you a QA Manager that has experience
Performing QA Duties to ensure manufacturing, testing and clinical trial activities that comply with GMP, GCP and other regulatory guidelines
- Document Control systems
- Change Controls
- CAPA - Corrective and Preventative actions
- Deviations & OOS reporting
- Compliant and recall handling
- Performing internal Audits
- Write and review of documents - SOPs, Qualification/validation reports and batch records
- Subject Matter Expert (SME) for QA according to relevant regulatory authority cGMP.
- Regulatory requirements that specifically apply for the manufacture and/or testing of cell therapy products and/or ATMP’s.
If you are on the lookout for a new exciting position with an exciting startup ATMP company, then look no further. Please apply with an up to date copy of your CV