CQV Specialist / Senior Validation Engineer
Description For CQV Specialist / Senior Validation Engineer
Verista, a leading life sciences solutions provider with 600 experts, is seeking a Senior CQV Engineer to join their team in Warren, NJ. This role focuses on commissioning and qualification activities for gas distribution systems supporting QC Environmental Monitoring. The position offers a competitive salary range of $80,465-$116,843 and comprehensive benefits.
The ideal candidate will have 5+ years of experience in CQV activities, with expertise in gas system validation and documentation. You'll be responsible for preparing and executing qualification protocols, coordinating sampling activities, and ensuring compliance with cGMP standards. Strong technical writing and organizational skills are essential.
Verista's culture emphasizes empowerment, client success, and continuous learning. They provide innovative solutions to help solve some of the world's most pressing healthcare challenges. The company offers excellent growth opportunities in a fast-paced, people-focused environment.
Benefits include comprehensive medical coverage, 401(k) with employer matching, paid time off, tuition reimbursement, and various insurance options. The position requires onsite work in Warren, NJ, where you'll collaborate with cross-functional teams and contribute to critical validation projects.
Join a company that values expertise, innovation, and making a difference in the life sciences industry. Your work will directly impact the quality and compliance of essential healthcare systems while working alongside dedicated professionals committed to excellence.
Responsibilities For CQV Specialist / Senior Validation Engineer
- Prepare and execute commissioning and qualification documentation
- Develop and execute protocols (IQ, OQ, PQ)
- Coordinate gas sampling activities
- Collaborate with QC and Quality Assurance teams
- Maintain documentation quality and accuracy
- Author and execute technical validation documentation
- Run test scripts and document results
- Make recommendations for design modifications
- Mentor less experienced team members
- Communicate effectively with clients
Requirements For CQV Specialist / Senior Validation Engineer
- Bachelor's degree in Engineering, Life Sciences, or related field
- 5+ years of experience in CQV activities
- Knowledge of QC EM processes, gas distribution systems, and sampling validation
- Strong skills in document authorship
- Experience in cGMP-regulated environments
- Excellent writing and organizational skills
- Proficiency in Microsoft Office tools
- Strong problem-solving and critical thinking skills
- GMP and Good Documentation Practice
- Strong interpersonal skills
- Must work onsite in Warren, NJ
Benefits For CQV Specialist / Senior Validation Engineer
- Competitive pay plus performance-based incentives
- Company-paid Life Insurance
- Short-Term and Long-Term Disability Insurance
- Medical, Dental & Vision insurances
- FSA, DCARE, Commuter Benefits
- Health Savings Account
- 401(k) Retirement Plan with Employer Matching
- Paid Time Off with Rollover Option
- Paid Holidays
- Sick Time
- Tuition Reimbursement
- Team Social Activities
- Employee Recognition
- Employee Referral Program
- Paid Parental Leave
- Paid Bereavement Leave
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