Veritas Search Group
Join to apply for the
Validation Engineer
role at
Veritas Search Group Join to apply for the
Validation Engineer
role at
Veritas Search Group Get AI-powered advice on this job and more exclusive features. This range is provided by Veritas Search Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$65.00/hr - $73.00/hr Direct message the job poster from Veritas Search Group This role requires candidates who are currently authorized to work in the U.S. without sponsorship, and C2C arrangements are not accepted. This role is fully on-site in Boston. Position Summary: The
Validation Engineer
will be responsible for executing Commissioning, Qualification, and Validation (CQV) activities in support of a Cell and Gene Therapy manufacturing environment. This role involves collaboration across departments and flexibility to support multiple validation initiatives in a dynamic setting. Key Responsibilities: Develop and implement Quality System documentation to establish robust validation practices. Author and execute URS, IQ, OQ, and PQ protocols in alignment with GDP guidelines and internal quality standards. Support qualification efforts for analytical instruments, automated manufacturing equipment, and facility systems. Perform analytical instrumentation qualifications in accordance with USP
and internal procedures. Conduct automation and computer system validation (CSV) assessments to ensure compliance with 21 CFR Part 11 and relevant regulatory standards. Coordinate with vendors to schedule and execute validation and test plans. Work collaboratively with internal teams to ensure safe and efficient execution of CQV activities. Provide validation support for process changes and ongoing improvement initiatives. Contribute to process validation activities including aseptic process simulations (APS), process performance qualifications, and material qualifications. Develop and validate sterilization cycles as applicable. Support Environmental Monitoring Performance Qualification (EMPQ) activities as needed. Maintain compliance with training requirements and ensure all validation activities meet SOPs, global standards, and cGMP guidelines. Uphold a “right-the-first-time” documentation approach and promote strong cross-functional partnerships. Ideal Candidates Will Have: 2+ years of relevant validation experience in GMP manufacturing or analytical laboratory settings; early-career professionals with strong foundational knowledge are encouraged to apply. Solid understanding of Computer System Validation (CSV) principles and regulatory requirements. Experience or familiarity with Environmental Monitoring Performance Qualification (EMPQ) is a plus. Exposure to equipment and process validation is preferred. Ability to manage multiple priorities and shift between projects based on evolving needs. Adaptability, attention to detail, and a proactive mindset in a fast-paced, regulated environment. Bachelor’s degree in Engineering, Life Sciences, or a related field, or equivalent practical experience. Working knowledge of GMP, ISO, GAMP, and ANSI standards. Please submit your resume and send to recruiters@vsearchgroup.com if you are interested. Thank you! Seniority level
Seniority level Mid-Senior level Employment type
Employment type Contract Job function
Industries Hospitals and Health Care Referrals increase your chances of interviewing at Veritas Search Group by 2x Get notified about new Validation Engineer jobs in
Boston, MA . Equipment Validation Engineer(Contract) 22222
Waltham, MA $72,800.00-$80,100.00 3 days ago Cambridge, MA $97,440.00-$155,904.00 2 weeks ago Acton, MA $89,000.00-$100,000.00 6 days ago Brockton, MA $95,000.00-$120,000.00 5 days ago Boston, MA $102,100.00-$111,700.00 3 days ago Marlborough, MA $94,000.00-$118,000.00 2 weeks ago Boston, MA $90,000.00-$107,000.00 3 days ago Boston, MA $72,800.00-$80,100.00 3 days ago Lexington, MA $132,000.00-$193,300.00 1 month ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Validation Engineer
role at
Veritas Search Group Join to apply for the
Validation Engineer
role at
Veritas Search Group Get AI-powered advice on this job and more exclusive features. This range is provided by Veritas Search Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$65.00/hr - $73.00/hr Direct message the job poster from Veritas Search Group This role requires candidates who are currently authorized to work in the U.S. without sponsorship, and C2C arrangements are not accepted. This role is fully on-site in Boston. Position Summary: The
Validation Engineer
will be responsible for executing Commissioning, Qualification, and Validation (CQV) activities in support of a Cell and Gene Therapy manufacturing environment. This role involves collaboration across departments and flexibility to support multiple validation initiatives in a dynamic setting. Key Responsibilities: Develop and implement Quality System documentation to establish robust validation practices. Author and execute URS, IQ, OQ, and PQ protocols in alignment with GDP guidelines and internal quality standards. Support qualification efforts for analytical instruments, automated manufacturing equipment, and facility systems. Perform analytical instrumentation qualifications in accordance with USP
and internal procedures. Conduct automation and computer system validation (CSV) assessments to ensure compliance with 21 CFR Part 11 and relevant regulatory standards. Coordinate with vendors to schedule and execute validation and test plans. Work collaboratively with internal teams to ensure safe and efficient execution of CQV activities. Provide validation support for process changes and ongoing improvement initiatives. Contribute to process validation activities including aseptic process simulations (APS), process performance qualifications, and material qualifications. Develop and validate sterilization cycles as applicable. Support Environmental Monitoring Performance Qualification (EMPQ) activities as needed. Maintain compliance with training requirements and ensure all validation activities meet SOPs, global standards, and cGMP guidelines. Uphold a “right-the-first-time” documentation approach and promote strong cross-functional partnerships. Ideal Candidates Will Have: 2+ years of relevant validation experience in GMP manufacturing or analytical laboratory settings; early-career professionals with strong foundational knowledge are encouraged to apply. Solid understanding of Computer System Validation (CSV) principles and regulatory requirements. Experience or familiarity with Environmental Monitoring Performance Qualification (EMPQ) is a plus. Exposure to equipment and process validation is preferred. Ability to manage multiple priorities and shift between projects based on evolving needs. Adaptability, attention to detail, and a proactive mindset in a fast-paced, regulated environment. Bachelor’s degree in Engineering, Life Sciences, or a related field, or equivalent practical experience. Working knowledge of GMP, ISO, GAMP, and ANSI standards. Please submit your resume and send to recruiters@vsearchgroup.com if you are interested. Thank you! Seniority level
Seniority level Mid-Senior level Employment type
Employment type Contract Job function
Industries Hospitals and Health Care Referrals increase your chances of interviewing at Veritas Search Group by 2x Get notified about new Validation Engineer jobs in
Boston, MA . Equipment Validation Engineer(Contract) 22222
Waltham, MA $72,800.00-$80,100.00 3 days ago Cambridge, MA $97,440.00-$155,904.00 2 weeks ago Acton, MA $89,000.00-$100,000.00 6 days ago Brockton, MA $95,000.00-$120,000.00 5 days ago Boston, MA $102,100.00-$111,700.00 3 days ago Marlborough, MA $94,000.00-$118,000.00 2 weeks ago Boston, MA $90,000.00-$107,000.00 3 days ago Boston, MA $72,800.00-$80,100.00 3 days ago Lexington, MA $132,000.00-$193,300.00 1 month ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr