Validation Engineer / CQV
Arthur Lawrence
Job Description
Job Description
**ONSITE**
Job SummaryWe are seeking a Validation Engineer to support validation, qualification, and calibration activities within a pharmaceutical manufacturing environment. This is an excellent opportunity for candidates with 3-5 years of experience in validation, CQV, or regulated industries who are looking to grow their career in pharmaceutical manufacturing and compliance.
Responsibilities
- Support equipment validation, qualification, and calibration activities
- Assist with execution of IQ/OQ/PQ protocols and validation documentation
- Ensure compliance with GMP and 21 CFR Part 11 requirements
- Support Computerized System Validation (CSV) activities
- Assist in validation of autoclaves, CIP skids, isolators, parts washers, and other manufacturing equipment
- Collaborate with Quality, Manufacturing, and Engineering teams to resolve validation issues
- Maintain accurate documentation and support audit readiness
Qualifications
- 3-5 years of experience in Validation, CQV, Calibration, or CSV
- Basic understanding of GMP and pharmaceutical compliance requirements
- Familiarity with IQ/OQ/PQ documentation and validation lifecycle
- Pharmaceutical, biotech, or regulated industry experience preferred
- Strong communication and problem-solving skills
- Bachelor’s degree in Engineering, Life Sciences, or related field preferred
Location: Boston, MA
Company DescriptionArthur Lawrence is a US-focused management consulting and staffing firm placing talent across IT, finance, light industries, and pharmaceuticals. We work with Fortune 500 clients and operate with a delivery-first mindset backed by a strong internal training culture.
Company Description
Arthur Lawrence is a US-focused management consulting and staffing firm placing talent across IT, finance, light industries, and pharmaceuticals. We work with Fortune 500 clients and operate with a delivery-first mindset backed by a strong internal training culture.
Vacancy posted 1 day ago
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