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Sterling Engineering is seeking a qualified Validation or Process Engineer for an onsite, long-term contract-to-hire role in Greenville, NC. The ideal candidate will have 5+ years of experience in aseptic processing, media fills, IQ/OQ/PQ, and sterile manufacturing within pharmaceutical settings.
You will perform hands-on process validation, PPQ, CPV, qualification, investigations, and GMP documentation. A Bachelor's degree in Engineering or a related technical field is required.
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
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.