A leading life sciences firm is seeking a professional focused on Commissioning, Qualification, and Validation (CQV) execution with a strong safety emphasis. Candidates should possess a Bachelor's degree in Engineering, Chemistry, or Life Sciences and have over three years of relevant experience in the Pharmaceutical/Life Sciences industry. Key responsibilities include project planning, documentation compliance, and vendor management. The role requires excellent communication skills and the ability to travel across the U.S. and possibly internationally. Benefits include comprehensive health coverage and a generous PTO policy.
Qualifications
3+ years of related experience in the Pharmaceutical/Life Sciences industry.
Essential experience in a GMP (Good Manufacturing Practice) environment.
Willingness and flexibility to travel throughout the U.S. and potentially internationally.
Responsibilities
Perform Commissioning, Qualification, and Validation (CQV) activities.
Support the generation and review of C&Q procedures.
Support planning of commissioning spares and consumables.
Skills
GMP experience
Outstanding communication skills
Problem-solving abilities
Customer-focused mindset
Flexibility to travel
Education
Bachelor’s degree in Engineering, Chemistry, or Life Sciences
Job description
A leading life sciences firm is seeking a professional focused on Commissioning, Qualification, and Validation (CQV) execution with a strong safety emphasis. Candidates should possess a Bachelor's degree in Engineering, Chemistry, or Life Sciences and have over three years of relevant experience in the Pharmaceutical/Life Sciences industry. Key responsibilities include project planning, documentation compliance, and vendor management. The role requires excellent communication skills and the ability to travel across the U.S. and possibly internationally. Benefits include comprehensive health coverage and a generous PTO policy.