CQV Engineer – Medical Device (6-Month Contract)

PSC Biotech; Columbia Township (MO); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical and Sick Time benefits

Job summary

PSC Biotech is seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to support capital projects at a medical device manufacturing facility in Columbia, MO. The ideal candidate will have at least five years of dedicated CQV experience in a regulated manufacturing environment and hands-on CQV activity.

The role involves developing and executing CQV protocols, coordinating with Engineering, Quality, and Manufacturing, and managing multiple projects with rigorous

Qualifications

• > 5 years of professional CQV experience in a regulated manufacturing environment.
• > Hands-on experience with commissioning, qualification, and validation activities.
• > Strong technical writing, documentation, and organizational skills.
• > Ability to manage CQV deliverables independently and work within cross-functional teams.

Responsibilities

• Plan, coordinate, and execute CQV activities for capital projects.
• Develop, review, and execute CQV protocols and documentation.
• Support qualification activities across project lifecycle (IQ/OQ/PQ).
• Review project documentation to ensure systems meet specs and validation requirements.
• Collaborate with Engineering, Quality, Manufacturing, and other stakeholders.
• Maintain CQV documentation in line with quality requirements.

Skills

CQV experience

Technical writing

Cross-functional collaboration

Education

Bachelor’s degree in Engineering or Life Sciences

Job description

PSC Biotech is seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to support capital projects at a medical device manufacturing facility in Columbia, MO. The ideal candidate will have at least five years of dedicated CQV experience in a regulated manufacturing environment and hands-on CQV activity.

The role involves developing and executing CQV protocols, coordinating with Engineering, Quality, and Manufacturing, and managing multiple projects with rigorous