ELIQENT Life Sciences is seeking a Process Validation Engineer to support pharmaceutical manufacturing projects, including new fill line implementation and revalidation activities. Responsibilities include developing validation strategies, coordinating aseptic media fills, and assisting with tech transfers.
The role emphasizes cGMP compliance, risk assessments, and CQV/documentation support, with a focus on aseptic processing environments and PFS lines. Flexible work arrangements are offered.
#J-18808-LjbffrPharma Process Validation Engineer - Flexible Work & Growth in greenville at Unknown Company
This position is listed as full time and onsite.