Regulatory Affairs Specialist (m/w/d)

Regulatory Affairs Specialist | Biberach an der Riß, Germany | Hybrid

This employer is seeking a dedicated Regulatory Affairs Specialist to join their team within the pharmaceutical industry. They are known for their commitment to excellence and fostering a collaborative environment, seeking to attract passionate professionals who want to make a significant contribution.

The Role

• Coordinate and oversee all activities involved in obtaining and maintaining product registrations.
• Review country-specific regulatory and normative requirements for product approvals.
• Conduct and prepare compliance testing for adherence to statutory regulations.
• Develop strategies, timelines, and documentation structures for regulatory submissions.
• Collaborate with German authorities, internal stakeholders, and external clients.
• Participate in project teams involving development, production, and product management.

What You'll Need

• University degree in Pharmacy, Medicine, or Natural Sciences; a pharmacist's license is highly desirable.
• Experience in Regulatory Affairs and experience with clinical trial application submissions.
• Profound knowledge of registration procedures.
• Excellent understanding of European and German pharmaceutical laws.
• Fluent in written and spoken German and English.
• Strong communication, negotiation skills, and a team-oriented mindset.
• High commitment and the ability to work independently and goal-orientedly.

What's On Offer

• Competitive salary and long-term job security through group affiliation.
• Comprehensive social benefits, including Christmas and vacation pay.
• Generous annual leave entitlement of up to 30 days.
• Individual training opportunities with renowned partners.
• Support in defining career goals and development pathways.

Apply via Haystack today!