What are the responsibilities and job description for the Validation Engineer position at Sterling Engineering?
Position: Validation Engineer / Process Engineer
Location: onsite in Greenville, NC
Duration: 12 months / contract to hire
I’m looking for an experienced Validation or Process Engineer with Aseptic, Sterile manufacturing for a long-term, contract-to-hire opportunity supporting pharmaceutical manufacturing.
The key is having at least five years of experience with
- aseptic processing, media fills, IQ/OQ/PQ, commercial manufacturing, or regulatory inspections
- Sterile/aseptic pharmaceutical manufacturing
- Oral solid dosage continuous manufacturing
- Hands-on experience with process validation, PPQ, CPV, qualification, validation protocols, investigations, and GMP documentation.
- Bachelor’s degree in Engineering or a related technical field required
About us…Sterling Engineering, in business for 57 years …we offer FULL BENEFITS! As a Sterling Engineering W2 employee on contract, you receive a Full Employee Benefits Package that includes Paid Time Off, Paid Holidays, 3 Medical plans to choose from, Dental & Vision plans, 401(k) with a match, and an Employee Stock Ownership (ESOP) plan.
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.
Salary : $50 - $70