MSAT Process Engineer - Biopharma Manufacturing Validation
ELIQUENT Life Sciences, Inc.
ELIQUENT Life Sciences, Inc. is seeking engineers to support life sciences manufacturing, validation, and documentation activities. The role covers process development, QC coordination, and regulatory-aligned reporting within a GMP environment. Responsibilities include pilot-scale filter press work, equipment testing, batch record updates, and cross-functional collaboration to ensure lifecycle documentation and validation deliverables meet quality standards. #J-18808-Ljbffr ELIQUENT Life Sciences, Inc.
Vacancy posted 2 days ago
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