Business Services & Consulting • all cities, MI 23
CQV Project Lead - Manufacturing Systems (23)
all cities, MI 23On-sitePosted 1 day ago
Business Services & Consulting
About the Role
CQV Project Lead – Manufacturing Systems
Position Overview: As a CQV Project Lead for Manufacturing Systems, you will oversee the commissioning, qualification, and validation (CQV) of life sciences manufacturing equipment and environments. Your role ensures that all manufacturing suites and equipment meet regulatory standards, focusing on maintaining product integrity and process reliability.
Key Responsibilities:
Lead CQV efforts for manufacturing systems including HVAC, BSCs, LFHs, autoclaves, parts washers, and single-use equipment (mixers, bioreactors).
Execute CQV protocols for Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Ensure validation of laboratory equipment (bench scales, pH meters, Vi-Cell analyzers) to support manufacturing processes.
Work closely with cross-functional teams to integrate CQV processes into daily manufacturing operations.
Required Qualifications:
Bachelor's degree in Life Sciences, Engineering, or related field.
5+ years of experience in manufacturing CQV in life sciences.
Knowledge of aseptic manufacturing practices, single-use systems, and GMP requirements.
CQV Project Lead – Manufacturing Systems
Position Overview: As a CQV Project Lead for Manufacturing Systems, you will oversee the commissioning, qualification, and validation (CQV) of life sciences manufacturing equipment and environments. Your role ensures that all manufacturing suites and equipment meet regulatory standards, focusing on maintaining product integrity and process reliability.
Key Responsibilities:
Lead CQV efforts for manufacturing systems including HVAC, BSCs, LFHs, autoclaves, parts washers, and single-use equipment (mixers, bioreactors).
Execute CQV protocols for Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Ensure validation of laboratory equipment (bench scales, pH meters, Vi-Cell analyzers) to support manufacturing processes.
Work closely with cross-functional teams to integrate CQV processes into daily manufacturing operations.
Required Qualifications:
Bachelor's degree in Life Sciences, Engineering, or related field.
5+ years of experience in manufacturing CQV in life sciences.
Knowledge of aseptic manufacturing practices, single-use systems, and GMP requirements.
What You'll Do
Lead CQV efforts for manufacturing systems including HVAC, BSCs, LFHs, autoclaves, parts washers, and single-use equipment (mixers, bioreactors).
Execute CQV protocols for Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Ensure validation of laboratory equipment (bench scales, pH meters, Vi-Cell analyzers) to support manufacturing processes.
Work closely with cross-functional teams to integrate CQV processes into daily manufacturing operations.
Bachelor's degree in Life Sciences, Engineering, or related field.
5+ years of experience in manufacturing CQV in life sciences.
