CQV Expert - Life Sciences
Developing innovative medicines requires reliable active ingredients.
* Main responsibilities include managing a team of commissioning and qualification engineers on-site, identifying commissioning and qualification strategies, and reviewing technical documentation to meet GMP and CQV requirements.
Familiar with mechanical completion procedures and construction scope of work. The role involves scheduling preparation and progress review.
Key Responsibilities:
* Manage team of commissioning and qualification engineers
* IDentify Commissioning and Qualification strategy
* Review technical documentation for GMP and CQV requirements
* Familiar with Mechanical Completion procedure
Requirements:
* Proven experience in life sciences
* Familiarity with GMP and CQV regulations
* Scheduling and project management skills
This is an exciting opportunity for professionals looking to grow their career in the life sciences industry.