Validation Engineering
Listed on 2026-02-21
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Pharmaceutical
Validation Engineer, Pharma Engineer -
Engineering
Validation Engineer, Pharma Engineer, Biomedical Engineer
GxP Associates is a rapidly expanding talent and workforce solutions provider specializing in supporting pharmaceutical, biotechnology, and medical device industries. We enable organizations to maintain compliance and execute critical projects by delivering highly skilled professionals in engineering, quality, validation, regulatory, and IT roles. With a deep understanding of regulated environments, we connect exceptional talent with innovative life sciences companies to drive success.
Our flexible delivery models and extensive candidate network ensure tailored solutions for client and partner needs, creating long-term value. At GxP Associates, we prioritize integrity, agility, and industry expertise to cultivate partnerships that foster growth and compliance in the life sciences sector.
Validation Engineer – Sterile / Injectable (W2 Contract Only) Duration: 12 Months (Strong Possibility of Extension)
GXP Associates is currently seeking an experienced Validation Engineer – Sterile / Injectable to support aseptic process validation activities for sterile injectable products in a cGMP manufacturing environment.
Note:
This is a W2 contract role only. C2C and 1099 candidates will not be considered.
- Support aseptic process validation for sterile injectable and vial filling operations
- Execute and document media fills, process validations, and cleaning validations
- Prepare and review IQ/OQ/PQ protocols and validation reports
- Support aseptic vial filling line validations (filling, stoppering, and capping)
- Participate in deviation investigations, CAPA, and risk assessments
- Ensure compliance with cGMP, FDA, and regulatory requirements
- Collaborate with Manufacturing, QA, and Engineering teams during validation execution
- 4–8 years of validation experience in sterile injectable manufacturing
- Hands-on experience with aseptic vial filling operations
- Strong experience in media fills and fill-finish validation
Solid understanding of cGMP and FDA regulations - Excellent documentation and technical writing skills
Interested candidates can share their updated resume to:
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