
Qualified Person - Pharmaceuticals - Remote Working
- Kingston upon Hull
- Permanent
- Full-time
- Act as a Named Qualified Person under the MIA licence, in compliance with EU GMP and UK regulatory standards.
- Perform final certification and batch release of medicinal products (both sterile and non-sterile, depending on experience).
- Review batch documentation, quality records, and deviation/CAPA reports as part of batch release process.
- Collaborate with Quality Assurance, Production, and Regulatory teams to ensure GMP compliance across the supply chain.
- Support inspections from the MHRA and other regulatory bodies as required.
- Provide expert QP input into quality system improvements and GMP compliance strategies.
- Eligible to act as a Qualified Person in the UK under Directive 2001/83/EC.
- Prior experience releasing products under an MIA licence is preferred
- Strong understanding of GMP and UK pharmaceutical regulatory frameworks.
- Excellent attention to detail and ability to work independently in a remote setting.
- Strong communication skills and a collaborative approach to cross-functional working.
- Remote working - achieve true work/life balance (1 day per month on site in England)
- Be part of a growing, quality-driven pharmaceutical business with a strong reputation.
- Join a forward-thinking organisation with a collaborative and supportive culture.