CQV Engineer / Validation Engineer- 5210
Description For CQV Engineer / Validation Engineer- 5210
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 and systems.
The position offers an opportunity to work with recognizable brands in the life science industry, focusing on solving critical healthcare challenges. As a CQV Engineer, you'll be responsible for technical commissioning, qualification, and validation documentation, while working in a GMP-regulated environment.
The ideal candidate will have a Bachelor's degree and experience in CQV activities specific to Process Equipment. Strong technical skills combined with excellent communication abilities are essential, as you'll be working closely with cross-functional teams and documenting complex processes.
Verista offers a culture that values empowerment, client success, and continuous learning. The company provides comprehensive benefits including competitive compensation, healthcare coverage, retirement benefits, and work-life balance programs. This is an excellent opportunity for someone looking to make an impact in the life sciences industry while working with a growing, innovative company.
The role offers significant growth potential in a fast-paced, people-focused organization. You'll be part of a team that's dedicated to improving lives through innovative solutions in the life sciences sector. The position requires working on-site in Indianapolis, allowing for direct collaboration with team members and hands-on involvement in critical projects.
Responsibilities For CQV Engineer / Validation Engineer- 5210
- 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 as part of a team
- 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
Requirements For CQV Engineer / Validation Engineer- 5210
- Bachelor's Degree or equivalent required
- Demonstrated experience in leading CQV activities specific to Process Equipment
- Proficiency using PC and Microsoft Office tools
- Strong problem-solving and critical thinking skills
- GMP and Good Documentation Practice
- Experience in GMP regulated environment
- Must be willing to work onsite in Indianapolis, IN
- Strong interpersonal skills and clear communication capabilities
- Proven attention to detail and organization in project work
- Capable of working on assigned tasks without mentorship
Benefits For CQV Engineer / Validation Engineer- 5210
- 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
Jobs Related To Verista CQV Engineer / Validation Engineer- 5210
