CQV Engineer / Validation Engineer - 5318
Description For CQV Engineer / Validation Engineer - 5318
Verista, a leading life sciences solutions provider with 600 experts, is seeking a CQV Engineer / Validation Engineer to join their team in Portland, Maine. This role offers an excellent opportunity for new or recent graduates in STEM fields to contribute to critical healthcare innovations. The position involves technical commissioning, qualification, and validation work in a GMP-regulated environment.
The ideal candidate will be responsible for executing validation documentation, running test scripts, and ensuring compliance with industry standards. This role combines technical expertise with practical implementation, requiring strong attention to detail and excellent communication skills. The position offers comprehensive benefits including healthcare coverage, 401(k) matching, and professional development opportunities.
Verista's culture emphasizes empowerment, client success, and continuous learning. The company provides innovative solutions to help solve some of the world's most pressing healthcare challenges. This role offers the opportunity to work in a fast-paced, growth-oriented environment while making a meaningful impact in the life sciences industry.
The position offers competitive compensation ranging from $59,951 to $79,000, along with extensive benefits including medical, dental, and vision insurance, paid time off, and tuition reimbursement. Join a team that values collaboration, professional growth, and work-life balance while contributing to meaningful healthcare solutions.
Responsibilities For CQV Engineer / Validation Engineer - 5318
- Author, edit, and execute technical commissioning, qualification and validation documentation
- Run test scripts and document results
- Maintain clear, detailed records qualification and validation
- Document impact and risk assessments
- Complete user interface testing, software verification, and alarm testing on automated systems
- Develop, review, and execute testing documentation
- Make recommendations for design or process modification based on test results
- Implement capital equipment and maintain process knowledge
Requirements For CQV Engineer / Validation Engineer - 5318
- Bachelor's or equivalent STEM degree (Biomedical Engineer, Chemical Engineer, etc.)
- Experience in leading CQV activities specific to Process Equipment
- Proficiency in Microsoft Office tools
- Strong communication and interpersonal skills
- Problem-solving and critical thinking skills
- Excellent organizational and time management skills
- Experience in GMP regulated environment
- Ability to work independently without mentorship
- Strong attention to detail
- Experience with high levels of challenge and change
Benefits For CQV Engineer / Validation Engineer - 5318
- 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
- Team Social Activities
- Paid Parental Leave and Bereavement
