Technical Source is currently in search of a Senior Validation Engineer for our pharmaceutical manufacturing client in the Raleigh-Durham-Chapel Hill Area. This is a long-term contract position that requires on-site work. There is a possibility of full-time conversion if internal headcount allows. The qualified candidate should have experience conducting CQV efforts in a Start-Up Pharmaceutical environment.
Responsibilities of the Senior Validation Engineer include:
- Prepare and Execute Commissioning Documents for Site Start-Up
- Validate Pharmaceutical Manufacturing Equipment for New Builds/Expansions
- Utilize Paperless Validation Software
- Communicate with Vendors and Teams On-Site
Qualifications of the Senior Validation Engineer include:
- Bachelor's Degree in Engineering or Related Field
- 5+ Years of Experience Validating Autoclaves, Washers, Isolators, etc.
- Experience with cGMP documentation and the entire Validation Life Cycle
- Experience Working a Greenfield Environment
*No C2C or Sponsorship is available at this time*
*Compensation will scale based on experience and fit*
