Des Moines, Iowa
•
Today
Overview: Seeking a Biopharmaceutical Validation Engineer to support commissioning, qualification, and validation (CQV) activities for GMP manufacturing equipment and integrated systems. The role requires a self-driven professional capable of authoring and executing validation documentation independently while ensuring compliance with cGMP standards and regulatory requirements. Key Responsibilities: Author, review, and execute commissioning and qualification protocols (IQ/OQ/PQ) for single-use
Easy Apply
Full-time, Part-time, Third Party, Contract






