At a Glance
- Tasks: Manage CMC timelines and ensure compliance with GMP regulations in a biotech setting.
- Company: Apsida Life Science, a dynamic clinical-stage biotechnology firm.
- Benefits: Competitive salary and the chance to work at the forefront of science and project management.
- Other info: Exciting opportunity for career growth in a fast-paced environment.
- Why this job: Join a team making a real difference in biotechnology and clinical supply management.
- Qualifications: 5+ years of experience and a relevant Bachelor's degree required.
The predicted salary is between 50000 - 70000 £ per year.
Apsida Life Science is seeking a skilled professional in the United Kingdom to support CMC program execution in a clinical‑stage biotechnology context. The role involves managing CMC timelines, procurement of clinical supplies, and ensuring compliance with GMP regulations.
The ideal candidate will have at least 5 years of experience in related fields and a Bachelor’s degree in relevant disciplines. This position offers an opportunity to work at the intersection of science and project management.
CMC Regulatory Manager: Phase 3 Readiness & Global Supply employer: Apsida Life Science
Apsida Life Science is an exceptional employer that fosters a collaborative and innovative work culture, where employees are empowered to make impactful contributions in the biotechnology sector. With a strong focus on professional development, we offer numerous growth opportunities and support for continuous learning, all while being located in the vibrant UK life sciences hub. Join us to be part of a team that values your expertise and is dedicated to advancing healthcare solutions.
