Sr. Validation Engineer (cGMP) - Project Farma
On-site · Raleigh, North Carolina, United States or Greenville, North Carolina, United States
Job Summary
Sr. Validation Engineer (cGMP) at Project Farma responsible for executing technical CQV tasks, protocol development and equipment testing under the Site Lead, ensuring regulatory compliance (FDA, GMP), authoring SOPs and specifications, and delivering high-quality validation deliverables for life-sciences projects. Will provide hands-on support, troubleshooting for clients, participate in project planning and reporting, and travel domestically to meet client needs. Collaboration with cross-functional teams and mentoring of less experienced members as part of site strategy and project execution.
Required Qualifications
- Bachelor’s Degree in Life Science, Engineering, or related discipline
- 1-5 years in consulting and/or engineering services
- Willingness to travel as required for client project assignments
- Authorized to work in the United States on a full-time basis
- No visa sponsorship will be provided
Additional Requirements
- We will not sponsor applicants for current or future work visas
- Cannot employ anyone with an invalid driver's license
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