Pharma CQV Validation Engineer | GMP

CAI; Sacramento (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading engineering firm in Sacramento, California, is seeking a candidate with a Bachelor's degree in Engineering, Chemistry, or Life Sciences. The role involves performing Commissioning, Qualification, and Validation (CQV) activities, supporting project planning, and coordinating with vendors. Ideal candidates will have 2+ years of experience in the Pharmaceutical industry and strong problem-solving skills. Flexibility to travel is required. The company promotes diversity and is an equal opportunity employer.

Qualifications

• 2+ years of experience in the Pharmaceutical/Life Sciences industry.
• Experience in a GMP (Good Manufacturing Practice) environment.
• Strong written and oral communication skills.

Responsibilities

• Perform Commissioning, Qualification, and Validation (CQV) activities with a focus on safety.
• Support planning of commissioning spares and consumables.
• Coordinate with project contractors and equipment vendors to execute required testing.

Skills

Communication skills

Problem-solving abilities

Customer-focused mindset

Ability to travel

Education

Bachelor’s degree in Engineering, Chemistry, or Life Sciences

Job description

A leading engineering firm in Sacramento, California, is seeking a candidate with a Bachelor's degree in Engineering, Chemistry, or Life Sciences. The role involves performing Commissioning, Qualification, and Validation (CQV) activities, supporting project planning, and coordinating with vendors. Ideal candidates will have 2+ years of experience in the Pharmaceutical industry and strong problem-solving skills. Flexibility to travel is required. The company promotes diversity and is an equal opportunity employer.