Validation Engineer - GMP, Quality & Process Improvement
1710 embecta medical iHoldrege, NE
Validation Engineer - GMP, Quality & Process Improvement
L6
1710 embecta medical iHoldrege, NE9 days ago
Industries
Pharmaceutical Preparation ManufacturingBiological Product (except Diagnostic) ManufacturingMedicinal and Botanical Manufacturingembecta is seeking a Site Validation Engineer in Holdrege, Nebraska to execute validation initiatives supporting product design, maintain the site validation process, and provide cross-functional Quality Systems/Engineering support.
You will develop and maintain the Validation Master Plan, lead risk assessments and DOE, train teams, approve validation protocols, and contribute to continuous improvement while ensuring compliance with 21 CFR 820 and ISO 13485.
Apply now
Level
LeadL6
Location
Holdrege, NE
Occupation
Validation Engineers
Industry
Pharmaceutical Preparation Manufacturing
Posted
9 days ago
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