CQV Engineer - Medical Device, 6-Month Contract

PSC Biotech; New York (NY); On-site; USD 76,000 - 103,000; Part time

Benefits offered by this job

Medical benefits

Sick time

Job summary

PSC Biotech in Columbia, MO is seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer for a six-month W2 contract to support capital projects in a regulated medical device environment. The role requires at least five years of CQV experience, strong documentation skills, and the ability to work cross-functionally to advance project timelines and quality compliance.

Local work authorization is required.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline.
• 5+ years of professional CQV experience within a regulated manufacturing environment.
• Demonstrated hands-on experience with commissioning, qualification, and validation activities.
• Experience supporting capital projects involving manufacturing equipment, systems, facilities, or utilities.
• Strong experience developing, reviewing, and executing CQV protocols and associated documentation.
• Ability to independently manage CQV deliverables and work effectively within cross-functional project teams.
• Strong technical writing, documentation, organization, and problem-solving skills.
• Experience within the medical device industry or a similarly regulated environment preferred.
• Must be authorized to work in the U.S.
• No C2C at this time.

Responsibilities

• Plan, coordinate, and execute commissioning, qualification, and validation activities supporting capital projects.
• Develop, review, and execute CQV documentation and protocols for equipment, systems, and facility-related projects.
• Support qualification activities throughout the project lifecycle, including installation, operational, and performance qualification, as applicable.
• Review project documentation to ensure systems and equipment meet defined specifications and validation requirements.
• Identify, document, and support the resolution of discrepancies, deviations, and qualification-related issues.
• Collaborate with Engineering, Quality, Manufacturing, and other cross-functional stakeholders to support successful project execution.
• Maintain accurate and complete CQV documentation in accordance with applicable quality and documentation requirements.
• Support multiple capital projects and adapt CQV activities based on project scope, priorities, and timelines.
• Provide technical CQV expertise and independently manage assigned qualification activities.

Skills

Cross-functional collaboration

Technical writing

Problem-solving

Education

Bachelor’s degree in Engineering, Life Sciences, or related discipline

Job description

PSC Biotech in Columbia, MO is seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer for a six-month W2 contract to support capital projects in a regulated medical device environment. The role requires at least five years of CQV experience, strong documentation skills, and the ability to work cross-functionally to advance project timelines and quality compliance.

Local work authorization is required.