Senior CQV Engineer / Lead Validation Engineer
Description For Senior CQV Engineer / Lead Validation Engineer
Verista, a leading life sciences solutions provider with 600 experts, is seeking a Senior CQV Engineer / Lead Validation Engineer to join their team in Athens, GA. This role offers an opportunity to work with renowned brands in the life science industry, focusing on solving critical healthcare challenges. The position requires extensive experience in GMP regulated environments, with responsibilities including validation protocol execution, project management, and technical documentation. The ideal candidate will have 6-10+ years of CQV experience, strong communication skills, and expertise in validation processes. Verista offers a comprehensive benefits package, competitive salary range of $87,780-$134,153, and a culture focused on empowerment, client success, and continuous learning. The role combines technical expertise with leadership responsibilities, making it ideal for professionals looking to make a significant impact in the healthcare and biotech sectors. The company's commitment to innovation, professional development, and work-life balance makes this an excellent opportunity for experienced validation engineers seeking career growth.
Responsibilities For Senior CQV Engineer / Lead Validation Engineer
- Coordinate scheduling and execute OPQ Validation Protocol
- Manage responsibilities on multiple simultaneous projects and clients
- Drive activities as client facing leader
- Design validation plans
- Work with equipment OEMs and installation vendors
- Maintain detailed records of qualification and validation
- Author and execute technical commissioning and validation documentation
- Run test scripts and document results
- Develop, review, and execute testing documentation
- Make recommendations for design or process modification
Requirements For Senior CQV Engineer / Lead Validation Engineer
- 6-10+ years of demonstrated CQV experience in GMP regulated environments
- Experience in Commissioning & Validation activities covering URS (GMP equipment)
- Experience authoring and executing FAT, SAT, IOQ, CSV Protocols
- Must be willing to work onsite in Athens, GA
- Strong interpersonal skills and clear communication capabilities
- Intermediate skills with WORD
- Basic skills with EXCEL and PowerPoint
- GMP and Good Documentation Practice training
- Proven attention to detail and organization
Benefits For Senior CQV Engineer / Lead Validation Engineer
- Competitive pay plus performance-based incentives
- Company-paid Life, 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
- Tuition Reimbursement
- Paid Parental Leave
- Employee Recognition Program
- Employee Referral Program
