CQV Engineer

Job Description: This position is responsible for the successful implementation and coordination of equipment and facilities validation programs in compliance to cGMPs, FDA requirements and company policy. Development and execution of equipment and facilities validation protocols is the primary responsibility of this position. Inherent is the responsibility to ensure the accuracy and completeness of each validation study and that each study is acceptable to FDA standards and requirements. Respon

Summary: The CQV Engineer will be responsible for executing commissioning, qualification, and validation testing activities in a GMP pharmaceutical manufacturing environment. This role is strictly focused on test execution, protocol execution, and documentation support for process and equipment validation. The engineer will support validation of autoclaves, parts washers, and isolator filling systems, as well as associated utilities and processes. This is a hands-on, field-based role focused on

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Career Category Engineering Job Description Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each