Qualified Person (QP)
Core
Certify and release pharmaceutical batches in compliance with UK/EU regulations and internal quality standards for fast dissolving tablets and analytical lab services.
Role type
Qualified Person (QP) for pharmaceutical manufacturing
Builds
Zydis® fast dissolving tablets and CMC pharmaceutical analytical lab services
Domain
Pharmaceuticals / Life Sciences
Required skills
batch certification, regulatory compliance (UK/EU GMP), deviation and complaint management, audit support, validation oversight, change control, root cause analysis, quality leadership
Preferred skills
independent quality authority decision-making, stakeholder influence, team coaching, risk-based judgment, shop-floor engagement
Technologies
electronic quality systems
Responsibilities
Certify and release batches; review and approve batch records and analytical data; oversee deviations, complaints, and investigations; support internal/external audits and regulatory inspections; provide quality leadership across cross-functional teams; support new product introductions and technology transfers.
Seniority
Senior, hands-on IC with leadership responsibilities
