- Full Time
- New Jersey, USA

Mantell Associates
Mantell Associates is partnered with a leading clinical manufacturing CDMO in their search for a Site Director to join their team.
Site Director – Responsibilities:
- Oversee day to day operations and GMP manufacturing activities
- Build out a large team of top manufacturing professionals
- Work directly with the COO and board in overseeing successful delivery of projects
- Continually lead the expansion of the facility and the wider business
Site Head – Requirements:
- Masters or PhD in the field of pharmaceutical or a Life Sciences discipline
- 10 years experience in GMP environment
- 7 years of management experience
- In depth knowledge of pharmaceutical processes and manufacturing
- Outstanding leadership with the ability to work autonomously or leading projects
Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact us at +44 (0)20 3854 7700.
Tagged as: Management, Operations, Project Management