CQV Engineer - Validation Engineer
Description For CQV Engineer - Validation Engineer
Verista, a leading life sciences solutions provider with 600 experts, is seeking a CQV Engineer - Validation Engineer to join their team in Indianapolis. This role is crucial in ensuring quality and compliance in life science processes through technical commissioning, qualification, and validation activities. The position offers a competitive salary range of $59,951-$80,000 and comprehensive benefits.
The ideal candidate will be responsible for executing validation documentation, running test scripts, and maintaining detailed records in a GMP-regulated environment. They will work on user interface testing, software verification, and alarm testing on automated systems. The role requires strong technical expertise combined with excellent communication and teamwork skills.
Verista's culture emphasizes empowerment, client success, and continuous learning. They offer extensive benefits including healthcare coverage, 401(k) matching, paid time off, and professional development opportunities. The company's mission focuses on enabling life sciences clients to improve lives through innovative solutions.
This hybrid position provides an opportunity to work with recognized brands in the life science industry while contributing to solving pressing healthcare challenges. The role offers growth potential in a fast-paced, people-focused organization that values work-life balance and professional development.
Responsibilities For CQV Engineer - Validation Engineer
- Authoring, editing, and executing technical commissioning, qualification and validation documentation
- Running test scripts and documenting results
- Maintaining clear, detailed records qualification and validation
- Documenting impact and risk assessments
- Completing user interface testing, software verification, and alarm testing on automated systems
- Developing, reviewing, and executing testing documentation
- Making recommendations for design or process modification based on test results
- Understanding validation documents, URS, IQ, OQ, PQ
Requirements For CQV Engineer - Validation Engineer
- Bachelor's Degree or equivalent required
- Demonstrated experience in leading CQV activities specific to Process Equipment
- Proficiency using PC and Microsoft Office tools
- Strong communication and interpersonal skills
- Ability to work as part of a team
- Strong problem-solving and critical thinking skills
- Excellent organizational and time management skills
- GMP and Good Documentation Practice experience
- Experience in GMP regulated environment
- Must be willing to work onsite in Indianapolis, IN
Benefits For CQV Engineer - 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
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