Technical Source is actively seeking a Senior Validation Engineer for our pharmaceutical manufacturing client in the Raleigh-Durham-Chapel Hill area. This is a long-term, on-site contract position with potential for full-time conversion, contingent upon internal headcount availability. The ideal candidate will have experience conducting CQV (Commissioning, Qualification, and Validation) activities within a startup pharmaceutical setting.
Responsibilities of the Senior Validation Engineer:
- Prepare and execute commissioning documentation for site startup.
- Validate pharmaceutical manufacturing equipment for new builds or expansions.
- Utilize paperless validation software.
- Coordinate with vendors and on-site teams.
Qualifications for the Senior Validation Engineer:
- Bachelor's degree in engineering or a related field.
- 5+ years of experience validating equipment such as autoclaves, washers, and isolators.
- Proficiency with cGMP documentation and the complete validation lifecycle.
- Experience in a greenfield environment.
*No C2C or Sponsorship is available at this time*
*Compensation will scale based on experience and fit*
