6366 - CQV Engineer / Validation Engineer

Description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Validation Engineer Responsibilities:

• Execute IQ/OQ protocols and support commissioning and qualification activities for equipment, utilities, and process systems
• Perform drawing walkdowns, P&ID verification, equipment/component verification, and weld verification activities
• Support MOC activities, system turnover, and field verification to ensure alignment with approved engineering documentation
• Assist with temperature mapping studies, SIP/CIP execution, and cycle development activities using validation tools and data loggers
• Identify, document, and support investigation and resolution of deviations, discrepancies, and non-conformances
• Maintain accurate GMP/GDP-compliant documentation and collaborate cross-functionally with Engineering, QA, Validation, and Operations teams to support project execution and operational readiness

Job Requirements:

• Bachelor’s Degree or equivalent required (STEM degree, Biomedical Engineering, Chemical Engineering preferred)
• 1-3 years of CQV, validation, commissioning, or related experience within pharmaceutical, biotech, or regulated manufacturing environments
• Experience executing IQ/OQ protocols and supporting commissioning/qualification activities
• Familiarity with GMP/GDP documentation practices and regulated industry requirements
• Ability to read and interpret P&IDs, engineering drawings, and technical documentation
• Experience supporting temperature mapping, CIP/SIP systems, and field verification activities preferred
• Strong organizational, communication, and problem-solving skills
• Ability to work independently in fast-paced project environments while managing multiple priorities simultaneously

This role requires the ability to be on-site, full-time in Devens, MA.

Benefits

Why Choose Verista?

• High growth potential and fast-paced organization with a people-focused culture
• Competitive pay plus performance-based incentive programs
• Company-paid Life, Short-Term, and Long-Term Disability Insurance.
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities (We have fun!)
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

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For more information about our company, please visit us at Verista.com