GxP Expert | Biologe (m/w/d)

Job Summary

This role is for a proactive GxP Expert who thrives on taking ownership and driving regulatory projects in the pharmaceutical and medical device sectors. The successful candidate will assume technical responsibility for regulatory projects within GMP and GDP environments, potentially acting as Head of QA or Wholesale Representative. Key responsibilities include overseeing functions related to Manufacturing and Import Authorisation (MIA), such as Head of Manufacturing or Head of Quality Control. The position requires not just implementing regulatory requirements but translating them into practical, economically viable processes. Building and evolving quality management systems, as well as conducting audits and supporting inspections, are also core duties. This is an attractive opportunity for someone who thinks independently, plans proactively, and acts decisively to make complex regulatory demands understandable and actionable for clients.