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 Equipment Validation in a Pharmaceutical environment.
Responsibilities of the Senior Validation 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 Validation 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*
