CQV Engineer / Validation Engineer
Description For CQV Engineer / Validation Engineer
Verista, a leading company in the life sciences industry with 600 experts, is seeking a CQV Engineer / Validation Engineer for their Tipp City, Ohio location. This role is integral to their mission of empowering growth and innovation within the scientific community. The position involves technical commissioning, qualification, and validation documentation for equipment, systems, and processes.
The ideal candidate will join a culture that values empowerment, client success, and continuous learning. You'll be responsible for conducting periodic reviews, assisting with VRB, managing change control duties, and performing root cause investigations. The role requires strong attention to detail, excellent documentation skills, and the ability to work independently.
Verista offers a comprehensive benefits package including competitive pay, medical/dental/vision insurance, 401(k) with employer matching, paid time off, and professional development opportunities. The company's commitment to improving lives through innovative solutions makes it an excellent choice for professionals seeking to make an impact in the life sciences industry.
The position offers growth potential in a fast-paced, people-focused organization. You'll work alongside dedicated professionals in a GMP-regulated environment, contributing to projects that help solve some of the world's most pressing healthcare challenges. The salary range of $59,951-$90,000 reflects the company's investment in top talent.
Responsibilities For CQV Engineer / Validation Engineer
- Authoring, editing, and executing technical commissioning, qualification and validation documentation
- Conduct Periodic Reviews
- VRB Assistance
- Administer Change control duties
- Conduct Root Cause Investigations
- Adherence with project schedule for all assigned activities
- Maintaining clear, detailed records qualification and validation
- Documenting impact and risk assessments as part of a team
- Making recommendations for design or process modification based on test results
Requirements For CQV Engineer / Validation Engineer
- Must be willing to work onsite at the client facility in Tipp City, OH
- Bachelor's Degree or equivalent required
- Demonstrated experience in executing CQV activities specific to Process Equipment
- General understanding of capital equipment implementation and process knowledge
- Proficiency using PC and Microsoft Office tools
- Strong problem-solving and critical thinking skills
- Excellent organizational and time management skills
- GMP and Good Documentation Practice
- Experience in GMP regulated environment
- Proven attention to detail and organization in project work
- Capable of working on assigned tasks without mentorship
Benefits For CQV Engineer / Validation Engineer
- 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
- Health Savings Account
- 401(k) Retirement Plan with Employer Matching
- Paid Time Off with Rollover Option and Holidays
- As Needed Sick Time
- Tuition Reimbursement
- Team Social Activities
- Employee Recognition
- Employee Referral Program
- Paid Parental Leave and Bereavement
