Validation Engineer - Instrument Qualification

Job Title:Validation Engineer - Instrument QualificationJob Function:Validation AnalystLocation:Los Angeles, CA. ...

Instrument QualificationJob Function:Validation AnalystLocation:Los Angeles, CA. ...

Job Title: Validation Engineer - Instrument Qualification Job Function: Validation Analyst Location: Los Angeles, CA USDM Life Sciences is a premier consulting company with 20+ years of experience assisting heavily regulated biotech, medical device, and pharmaceutical ...

Job Title: Validation Engineer - Instrument Qualification Job Function: Validation Analyst Location: Los Angeles, CA. Perform qualification activities for analytical instruments, including IQ/OQ/PQ (Installation, Operational, and Performance Qualification) following established protocols and regulat...

We arehiring an experienced CQV Engineer to support the commissioning,qualification, and validation for a range of facility equipment and systems within thepharmaceutical and/or biotechnology industry. Lead the development and executionof commissioning, qualification, and validation protocols for pl...

We are hiring an experienced CQV Engineer to support the commissioning, qualification, and validation for a range of facility equipment and systems within the pharmaceutical and/or biotechnology industry. Lead the development and execution of commissioning, qualification, and validation protocols fo...

We are hiring an experienced CQV Engineer to support the commissioning, qualification, and validation for a range of facility equipment and systems within the pharmaceutical and/or biotechnology industry. Lead the development and execution of commissioning, qualification, and validation protocols fo...

We are hiring an experienced CQV Engineer to support the commissioning, qualification, and validation for a range of facility equipment and systems within the pharmaceutical and/or biotechnology industry. Lead the development and execution of commissioning, qualification, and validation protocols fo...

Must have knowledge of current industry expectations of validation requirements for IQ/OQ/PQ/Cleaning/Equipment validations. Actively participate during all phases of validation including documents for IQ/OQ. Maintain system that tracks validation records. Write, review and approve validation strate...

Additionally, this role evaluates technology and process improvements and plays a key role in process understanding and process characterization. Additionally, the process engineer will be involved in manufacturing support and technology transfer to ensure successful implementation in a cGMP environ...