Mid Level CQV Engineer Jobs
Mid level cqv engineer jobs go to professionals ready to own qualification protocols end to end, guide junior engineers through execution, and make technical decisions without constant oversight. Openings run predominantly on-site across Consulting & Professional Services, Manufacturing, and Biotechnology & Pharmaceuticals, with employers like Katalyst Healthcares & Life Sciences, Hovione, and Verista hiring at this level now.
Find Mid Level CQV Engineer JobsOverview
Showing 5 of 8+ Mid Level CQV Engineer jobs
We are seeking an experienced Equipment CQV Engineer to support an GMP equipment commissioning and qualification program at a biopharmaceutical manufacturing facility in Massachusetts. The engineer will be responsible for hands-on execution of equipment commissioning, qualification, and validation activities across manufacturing, laboratory, and facility support equipment.
Roles and Responsibilities
- Execute equipment commissioning and qualification activities in accordance with approved GMP procedures and qualification protocols.
- Review and execute IQ, OQ, and other equipment qualification protocols.
- Perform hands-on testing and verification of manufacturing, laboratory, and support equipment.
- Document test results, observations, and qualification activities accurately and in compliance with Good Documentation Practices (GDP).
- Identify, investigate, and support resolution of discrepancies, deviations, and protocol execution issues.
- Prepare and review qualification documentation, including test records, equipment documentation, and supporting evidence.
- Work closely with Engineering, Validation, Manufacturing, Quality Assurance, and equipment vendors to ensure equipment readiness.
- Support equipment turnover and readiness activities for manufacturing and engineering operations.
- Ensure qualification activities are performed in accordance with applicable GMP, SOP, and site validation requirements.
- Manage multiple equipment qualification packages and complete assigned activities within project timelines.
- Participate in troubleshooting and resolution of equipment-related qualification issues.
- Support change controls, deviations, CAPAs, and other quality-system activities as required.
- Maintain clear and complete qualification records and ensure documentation is audit-ready.
- Communicate qualification status, execution issues, and project risks to relevant stakeholders.
- Bachelor's degree in engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related technical discipline.
- Equivalent combination of education and relevant industry experience may be considered.
- Approximately 5 10 years of experience in CQV, equipment validation, equipment qualification, commissioning, or a related field.
- Strong hands-on experience executing IQ/OQ and other equipment qualification protocols.
- Experience working in GMP-regulated pharmaceutical, biotechnology, biopharmaceutical, cell therapy, or life sciences manufacturing environment.
- Experience qualifying manufacturing, laboratory, utility, or other GMP equipment.
- Demonstrated ability to review protocols, execute testing, document results, and resolve discrepancies or deviations.
We are seeking an experienced Equipment CQV Engineer to support an GMP equipment commissioning and qualification program at a biopharmaceutical manufacturing facility in Massachusetts. The engineer will be responsible for hands-on execution of equipment commissioning, qualification, and validation activities across manufacturing, laboratory, and facility support equipment.
Roles and Responsibilities
- Execute equipment commissioning and qualification activities in accordance with approved GMP procedures and qualification protocols.
- Review and execute IQ, OQ, and other equipment qualification protocols.
- Perform hands-on testing and verification of manufacturing, laboratory, and support equipment.
- Document test results, observations, and qualification activities accurately and in compliance with Good Documentation Practices (GDP).
- Identify, investigate, and support resolution of discrepancies, deviations, and protocol execution issues.
- Prepare and review qualification documentation, including test records, equipment documentation, and supporting evidence.
- Work closely with Engineering, Validation, Manufacturing, Quality Assurance, and equipment vendors to ensure equipment readiness.
- Support equipment turnover and readiness activities for manufacturing and engineering operations.
- Ensure qualification activities are performed in accordance with applicable GMP, SOP, and site validation requirements.
- Manage multiple equipment qualification packages and complete assigned activities within project timelines.
- Participate in troubleshooting and resolution of equipment-related qualification issues.
- Support change controls, deviations, CAPAs, and other quality-system activities as required.
- Maintain clear and complete qualification records and ensure documentation is audit-ready.
- Communicate qualification status, execution issues, and project risks to relevant stakeholders.
- Bachelor's degree in engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related technical discipline.
- Equivalent combination of education and relevant industry experience may be considered.
- Approximately 5 10 years of experience in CQV, equipment validation, equipment qualification, commissioning, or a related field.
- Strong hands-on experience executing IQ/OQ and other equipment qualification protocols.
- Experience working in GMP-regulated pharmaceutical, biotechnology, biopharmaceutical, cell therapy, or life sciences manufacturing environment.
- Experience qualifying manufacturing, laboratory, utility, or other GMP equipment.
- Demonstrated ability to review protocols, execute testing, document results, and resolve discrepancies or deviations.
See All 8 Mid Level CQV Engineer Jobs
Find roles that match your experience and apply in just a few clicks.
Find Mid Level CQV Engineer JobsMid Level CQV Engineer Job Market
Who's Hiring
Top Industries Hiring
- Consulting & Professional Services
- Manufacturing
- Biotechnology & Pharmaceuticals
Mid Level CQV Engineer Jobs: Frequently Asked Questions
How do I get a mid level cqv engineer job?
Position yourself around ownership, not just participation. Highlight protocols you led from IQ through PQ, any deviation investigations you resolved independently, and GMP documentation you authored rather than assisted with. Employers at this level want engineers who can run a qualification campaign with minimal direction, so your application and interviews should center on specific systems you qualified and the decisions you drove.
Which companies hire mid level cqv engineers?
Companies hiring mid level cqv engineers right now include Katalyst Healthcares & Life Sciences, Hovione, and Verista, based on current listings on Migrate Mate as of November 2026. Hiring at this level is concentrated among pharmaceutical manufacturers, biologics CDMOs, and medical device firms that run active validation programs across cleanroom and manufacturing environments.
Are there remote mid level cqv engineer jobs?
Yes, though most cqv work remains tied to physical facilities. About 0% of mid level cqv engineer openings are remote or hybrid as of November 2026, and those roles typically involve documentation, protocol writing, or regulatory support rather than hands-on equipment qualification. If flexibility matters to you, filter for hybrid openings where on-site days are defined upfront.
How do I move up to a mid level cqv engineer role?
Moving from entry level into a mid level cqv engineer role comes down to deepening your hands-on qualification experience and taking ownership of outcomes. Build a record of running IQ, OQ, and PQ phases from start to finish, writing and defending protocols under audit conditions, and resolving non-conformances independently. Demonstrating measurable impact, such as reducing cycle time on a qualification or catching a critical deviation, signals readiness for mid level responsibilities.
Which industries hire the most mid level cqv engineers?
Mid Level cqv engineer roles concentrate in Consulting & Professional Services, Manufacturing, and Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of November 2026. These sectors drive consistent demand because their regulated manufacturing environments require ongoing qualification, revalidation, and process change control work that mid level engineers are well positioned to lead independently.