Senior CQV Engineer
Technical Source is currently in search of a Senior CQV 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 CQV Engineer include :
- Validate Pharmaceutical Manufacturing Equipment
- Prepare and Execute Commissioning Documents
- Utilize Paperless Validation Software
- Communicate with Vendors and Teams On-Site
Qualifications of the Senior CQV Engineer include :
- Bachelor's Degree in Engineering or Related Field
- 5+ Years of Validation Experience
- Experience with cGMP documentation and the entire Validation Life Cycle
- No C2C or Sponsorship is available at this time*
- Compensation will scale based on experience and fit*
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