Responsibilities: Develop global regulatory CMC strategies for enterprise-wide CAPEX and compliance projects through collaboration with functional leaders in Global Regulatory Affairs CMC, Global Regulatory Affairs, R&D, Quality, Global Operations, and other business functions. Assess and facilitate the
Production Operator – GMP / Biotech Manufacturing (m/f/d) Shape the future of Life Sciences with Techfirm Engineering Techfirm Engineering is looking for a Production Operator with solid experience in GMP-regulated manufacturing, ideally within a biotechnology environment.