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QA Specialist
3 weeks ago
The main purpose of your role will be:
- Performs activities for the batch release process to ensure all documentation is checked and available for QP release to meet the OTIF requirements.
- Performs activities for Disposition of raw materials and packaging and to ensure all materials are available when required.
- Performs QA activities to ensure documentation reviews and feedback are performed in a timely manner.
- Performs QA activities to ensure the sites ongoing FUST Stability programme is met.
- Deviation Management and CAPA system(s). Participate in Investigates, provide guidance, report and approve operational deviations, working with internal stakeholders & external partners to resolve issues and identify effective CAPA’s in a timely manner.
- Review, advise and approve effective change control actions across the Dundee Facility ensuring compliance with the necessary regulations.
- Write/revise/approve and give advice on quality documentation (i.e. batch records, product specifications, packaging specifications, annual product quality reviews, stability & validation protocol(s)), Raw Material specs, Finished Product Specifications, MOAs
Your Background:
- Science Degree (Chemistry, Pharmacy or Biology).
- Experience in a similar role.
- Private Health insurance.
- Optional Family Health Insurance.
- Flexible Employee Pension Contributions.
- Group Income protection.
- Cycle to Work Scheme.
- Tech Scheme.
- Death in Service.
- Free Car Parking.
- EAP.
- Friday Dress Down Day.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 103743 in all correspondence.
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