Pharmaceutical Project Manager
We are seeking an experienced project manager to oversee the management of a team of C&Q Engineers on high profile client sites throughout the project lifecycle.
The key responsibilities include:
* Managing Validation Master Plans, Commissioning Master Plans and project procedures
* Design Review (DR) process and GMP Risk Assessment (FMEA)
* Identifying Commissioning and Qualification strategies and defining activities required
* Reviewing technical documentation for alignment with GMP and CQV requirements
* Investigating and resolving technical issues with assistance from engineers and/or suppliers
The ideal candidate will have:
* 10+ years of experience in commissioning and qualification activities for pharmaceutical facilities
* Strong leadership and team player ability, liaising directly with clients and other project key functions
* Previous experience as manager/leader of C&Q teams
* Strong knowledge of ISPE and ASTM E2500
Key Benefits:
This is a long term contract role with a minimum duration of 12 months, offering competitive hourly rates between €80-€90 per hour.