Responsibilities
- Provide quality oversight and GMP compliance guidance for manufacturing, lab testing, and material management.
- Deliver on-site support for production and lab operations, managing deviations, change controls, CAPAs, and training.
- Review and approve master records for batch manufacturing, cleaning, and analytical processes.
- Oversee the issuance and evaluation of executed batch and cleaning records to ensure procedural compliance.
- Act as a quality reviewer for SOPs, protocols, reports, and change requests.
- Ensure validation and compliance of facility utilities, environmental monitoring, and cleaning processes.
- Participate in meetings to monitor data trends, resolve deviations, and assess quality impacts.
Requirements
- Bachelor's degree in Pharmaceutical Sciences or similar.
- 3+ years of experience in the pharmaceutical industry.
Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
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