Upstream CQV Lead Engineer - Bioprocess Validation
Verista, Inc.
A leading life sciences firm in Holly Springs, NC is seeking a CQV Engineer to support commissioning, qualification, and validation for biopharmaceutical manufacturing operations. The ideal candidate will have hands-on experience in upstream bioprocessing systems, strong communication skills, and familiarity with validation documentation. This role requires collaboration across engineering and quality teams to ensure compliance with cGMP standards. Competitive compensation and growth opportunities are offered in a fast-paced environment. #J-18808-Ljbffr Verista, Inc.
Vacancy posted 2 days ago
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