Senior Qualified Person – mRNA Biologics (UK Site)

Moderna; City of Edinburgh; On-site; GBP 70,000 - 90,000; Full time

Job summary

A leading biotech firm in Edinburgh is seeking a Qualified Person to ensure compliance with strict regulatory standards for mRNA-based drug products. The role involves certifying batch releases, maintaining a robust Pharmaceutical Quality System, and driving a quality culture across the organization. Ideal candidates should have a life science degree, at least 10 years of experience in the industry, and the ability to influence cross-functional teams in a GMP-regulated environment. This full-time position includes competitive benefits and emphasizes collaboration for global health initiatives.

Benefits

Best-in-class healthcare

Generous paid time off

Family building benefits

Qualifications

• 10 years’ experience in quality roles within the biotechnology or pharmaceutical industry.
• Eligibility to act as a Qualified Person with knowledge of biologics and sterile manufacturing.
• Experience working in GMP-regulated pharmaceutical production.

Responsibilities

• Certifying batch releases for compliance with regulations.
• Maintaining oversight of the Pharmaceutical Quality System.
• Leading or participating in regulatory inspections and audits.

Skills

Expert knowledge of Pharmaceutical Quality Management Systems

Demonstrated ability to influence cross-functional teams

Strong communicator and collaborator

Commitment to maintaining QP status

Education

Life science degree and/or relevant postgraduate qualification

Job description

A leading biotech firm in Edinburgh is seeking a Qualified Person to ensure compliance with strict regulatory standards for mRNA-based drug products. The role involves certifying batch releases, maintaining a robust Pharmaceutical Quality System, and driving a quality culture across the organization. Ideal candidates should have a life science degree, at least 10 years of experience in the industry, and the ability to influence cross-functional teams in a GMP-regulated environment. This full-time position includes competitive benefits and emphasizes collaboration for global health initiatives.