CQV Engineer

Job Title: CQV Engineer Locations: Mesa, AZ Duration: 6+ MonthsRole OverviewWe are seeking experienced CQV Engineers to support qualification and validation activities for sterile and non-sterile manufacturing systems within pharmaceutical operations. This role will focus on equipment qualification, protocol development/execution, and collaboration with vendors and cross-functional teams.Key ResponsibilitiesSupport commissioning, qualification, and validation (CQV) activities for manufacturing equipment and systems Execute and support equipment qualification activities including IQ/OQ/PQPerform temperature mapping activities for controlled equipment and environments Write, review, and execute qualification and validation protocols Participate in vendor meetings and provide technical CQV support Coordinate with Quality, Engineering, Validation, and Manufacturing teams Ensure compliance with GMP and project documentation requirements Equipment & Systems ExperienceAutoclaves Freezers Washers Fillers Sterile and non-sterile manufacturing equipment Required Qualifications5-7 years of CQV/Validation experience within pharmaceutical or biotech environments Strong experience with sterile and non-sterile systems Hands-on qualification and validation experience for GMP equipment Experience performing temperature mapping activities Ability to independently write and review validation documentation and protocols Strong communication and cross-functional coordination skills

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