CQV Engineer (New Grad)
Verista, Inc.
Salary undisclosed
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Description
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
CQV Engineer Responsibilities:
- Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader
- Running test scripts and documenting results
- Adherence with project schedule for all assigned activities
- Maintaining clear, detailed records qualification and validation
- Documenting impact and risk assessments as part of a team
- 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 when executing test scripts
- General understanding of capital equipment implementation and process knowledge
- Understanding validation documents, URS, IQ, OQ, PQ
Requirements
- Must be willing to work onsite in Columbus, OH
- Bachelor’s Degree or equivalent required (STEM degree highly preferred)
- Demonstrated experience in leading CQV activities specific to Process Equipment
- Proficiency using PC and Microsoft Office tools
- Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
- Ability to work as part of a team
- 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 (authoring/editing large technical documents with styles, tables, TOCs, track changes)
- Basic skills with EXCEL and PowerPoint
- Strong interpersonal skills and clear communication capabilities
- Experience with and tolerance for high levels of challenge and change
- Experience in GMP regulated environment
- Proven attention to detail and organization in project work
- Capable of working on assigned tasks without mentorship
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
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com
About this role
Verista is looking for a new graduate to join its Columbus office as a CQV Engineer, supporting the company's work with major life sciences clients on equipment validation and process qualification. In this role, you'll author and execute technical documentation for commissioning, qualification, and validation activities—running test scripts, documenting results, and conducting user interface and software verification testing on automated systems. You'll work as part of a project team, maintaining detailed records, assessing risks and impacts, and making recommendations for design or process improvements based on your findings.
The position calls for a STEM degree holder with a solid grasp of GMP and good documentation practices, intermediate proficiency in Word for large technical documents, and basic Excel and PowerPoint skills. You'll need strong communication and problem-solving abilities, meticulous attention to detail, and the capacity to work independently on assigned tasks. Prior experience in a GMP-regulated environment and familiarity with capital equipment implementation are expected; this is not an entry-level mentorship role.
Verista offers competitive pay with performance incentives, comprehensive health and retirement benefits, tuition reimbursement, paid parental leave, and a collaborative, fast-paced culture. The role is in-office only in Columbus, Ohio.
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