Found Description
Lavipharm is seeking a Specialist Product Release / QP based in Athens, reporting to the Manager Quality Operations. The successful candidate will be responsible for the final review and certification of batches for release to market, acting in accordance with Directive 2001/83/EC and the obligations of a Qualified Person under EU GMP.
Key Responsibilities:
- Personal, non-delegable accountability for batch certification — you will be the signing QP under Directive 2001/83/EC and Annex 16, exercising independent professional judgement on every release decision, not executing a team-delegated task.
- Final independent quality verification before commercial release — the role sits between QA Operations team activity and the market, providing the critical assurance layer that every batch meets its MA dossier, GMP requirements, and applicable national obligations.
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