Enable cross-functional awareness of global regulatory milestones to support operational readiness
Support documentation transfer and adaptation efforts for established products across various markets
Contribute to global authorization processes by assembling technical content and compliance documentation
Maintain alignment between site operations and regulatory functions at regional and global levels
Provide functional expertise during compliance assessments and regulatory inspections
Utilize digital platforms to manage documentation and support process development initiatives
Understanding of global regulations and awareness of health authority and industry developments advantageous
Experience with internal data management and documentation systems required
Strong proficiency in both written and spoken German and English highly recommended
Hybrid work model and flexible working hours
Permanent employment contract
Competitive remuneration package, including bonus payments such as holiday and year-end bonuses
Well-structured and thorough onboarding process
Access to exclusive employee discounts through established partner programs
Exposure to leading international companies and corporate environments
Interested in the role of Regulatory Specialist (m/f/d) – Pharma / CMC?
Apply now via our online application form!