Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
- We empower and support our colleagues
- We commit to client success at every turn
- We have the courage to do the right thing
- We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
- We constantly acquire new skills and learn from our experiences to enhance our collective expertise
Job Overview: We are seeking CQV Engineers with at least 3 years of direct CQV experience to support execution of GMP equipment qualification deliverables. These roles will focus on protocol execution, documentation, discrepancy support, data capture, and qualification package completion under the direction of senior CQV leads.
Validation Engineer Responsibilities:
- Execute CQV protocols, readiness checklists, IOQ/PQ testing, and related qualification activities
- Document execution results in accordance with GMP expectations
- Support vendor qualification wrapper executions
- Identify, document, and support resolution of discrepancies
- Assist with QSR generation and closeout package assembly
- Coordinate with senior CQV engineers, equipment leads, SMEs, and quality reviewers
- Maintain accurate and complete GMP documentation
- Support both Phase 1 RAMP Readiness and Phase 2 Sustained Readiness execution needs
Job Requirements:
- Bachelor's Degree or equivalent required
- Minimum 3 years direct CQV experience
- Experience executing equipment qualification protocols in GMP environments
- Familiarity with IQ/OQ/PQ, readiness checklists, deviations, and QSR support
- Strong attention to detail and GMP documentation discipline
- Biologics or pharmaceutical manufacturing experience
- Experience with lab equipment, CTUs, process equipment, single-use systems, or analytical instruments
- Experience with ValGenesis or similar systems
This role requires the ability to be on-site, full-time in Devens, MA.
Benefits
Why Choose Verista?
- High growth potential and fast-paced organization with a people-focused culture
- 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
- Supplemental Life, Hospital, Critical Illness and Legal Insurance
- Health Savings Account
- 401(k) Retirement Plan (Employer Matching benefit)
- Paid Time Off (Rollover Option) and Holidays
- As Needed Sick Time
- Tuition Reimbursement
- Team Social Activities (We have fun!)
- Employee Recognition
- Employee Referral Program
- Paid Parental Leave and Bereavement
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For more information about our company, please visit us at Verista.com
