Senior CQV Engineer - Senior Validation Engineer
Description For Senior CQV Engineer - Senior Validation Engineer
Verista is seeking a Senior CQV Engineer to join their team in Columbus, Ohio. This role involves designing validation plans, conducting impact and risk assessments, and maintaining detailed records of qualification and validation activities. The ideal candidate will have 4-6 years of relevant experience, a Bachelor's degree, and strong skills in communication, problem-solving, and GMP practices.
Key responsibilities include:
- Designing and executing engineering studies for critical process parameter definition
- Authoring and executing technical commissioning, qualification, and validation documentation
- Running test scripts and documenting results
- Completing user interface testing and software verification
- Developing and reviewing testing documentation
The company offers a competitive benefits package including medical, dental, and vision insurance, 401(k) with employer matching, paid time off, and tuition reimbursement. Verista values empowerment, client success, and continuous learning, making it an excellent opportunity for growth in the life sciences industry.
Salary range: $59,951 - $103,860
Join Verista to make an impact in solving some of the world's most pressing healthcare challenges while working with a team of dedicated professionals in a fast-paced, people-focused culture.
Responsibilities For Senior CQV Engineer - Senior Validation Engineer
- Designing validation plans
- Conducting and documenting impact and risk assessments
- Maintaining clear, detailed records of qualification and validation activities
- Designing and executing engineering studies for critical process parameter definition
- Authoring, editing, and executing technical commissioning, qualification and validation documentation
- Running test scripts and documenting results
- Completing user interface testing, software verification, and complete alarm testing on automated systems
- Developing, reviewing, and executing testing documentation
- Making recommendations for design or process modification based on test results
Requirements For Senior CQV Engineer - Senior Validation Engineer
- Bachelor's Degree or equivalent
- 4 - 6 years of demonstrated role relevant experience
- Experience in GMP regulated environment
- Proficiency using PC and Microsoft Office tools
- Strong problem-solving and critical thinking skills
- Excellent organizational and time management skills
- Strong attention to detail
- GMP and Good Documentation Practice
- Intermediate skills with WORD
- Basic skills with EXCEL and PowerPoint
- Strong interpersonal skills and clear communication capabilities
- Experience with and tolerance for high levels of challenge and change
Benefits For Senior CQV Engineer - Senior 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 (Employer Matching benefit)
- Paid Time Off (Rollover Option) and Holidays
- As Needed Sick Time
- Tuition Reimbursement
- Paid Parental Leave and Bereavement
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