Cpl Life Sciences is partnering with a leading global pharmaceutical company to appoint a Senior Manager, CMC Regulatory Affairs. You will lead global CMC regulatory strategies across development and commercial products, working with cross-functional teams to align with regulatory expectations.
The role offers exposure to late-stage development, global registrations and lifecycle management, with a hybrid 2-days onsite arrangement in Hertfordshire and a strong emphasis on collaboration with
Senior Manager, CMC Regulatory Affairs (Hybrid) employer: Cpl Life Sciences
Cpl Life Sciences is an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the biotechnology sector. With a strong focus on employee growth and development, team members benefit from hybrid working arrangements in West London, allowing for a balanced work-life integration while contributing to groundbreaking projects in regulatory affairs. The company values continuous improvement and provides opportunities for meaningful contributions to the advancement of healthcare solutions.
