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Systems Engineer @ Actalent

Plainville, Connecticut, USOnsiteContract
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About this role

Embrace the role of a Systems Verification and Validation Engineer II, where you'll ensure compliance with cGMP standards, manage engineering documentation, and collaborate with cross-functional teams in a highly regulated biopharmaceutical environment. Leverage your CAD expertise and attention to detail to support quality and regulatory excellence in a dynamic, fast-paced setting.. Category: Manufacturing, Mechanical, & Electrical

Skills

cad draftingengineering documentationcgmp complianceadept cad systemedmscmms (blue mountain)document controlfacility layout drawingsutilities systems documentationspare parts documentationcapa supportchange controlaudit-ready documentationproject coordinationtask prioritization

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