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!