Regulatory Affairs Specialist Location: Oss The Regulatory Affairs (RA) Specialist within the Development & Manufacturing department, ADS Licensing, is responsible for the preparation, review, and maintenance of high-quality regulatory submission documents describing the chemistry, manufacturing, and controls (CMC) aspects of
QA/RA Expert | Scinvivo Location: Eindhoven, NL Hybrid: minimal 3 days/week at the office Reports to: CEO and co-founder Marijn van Os Compensation: Competitive salary + potential equity participation after 1 year About the Venture -
Job TitleClinical Development Scientist Job Description Job Responsibilities Owns and drives end‑to‑end clinical evidence strategy, defining and linking clinical need, value, TPP, claims, endpoints, and evidence to regulatory acceptance and post‑market requirements with full lifecycle traceability (AD