6513 - Senior Validation Engineer / Senior CQV Engineer

Verista, Inc.; North Carolina; On-site; USD 79,000 - 129,000; Full time

Benefits offered by this job

Life/Disability Insurance

Medical/Dental/Vision Insurance

401(k) Matching

Paid Time Off

Tuition Reimbursement

Parental Leave

Job summary

Verista, Inc. is seeking a Senior Validation / CQV Engineer in the United States to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment, systems, software, and processes as part of a project team.

You will run test scripts, maintain detailed records, and ensure adherence to schedules while collaborating with peers in regulated packaging environments. A Bachelor’s degree and 5+ years of CQV experience, GMP training, and proficiency with

Qualifications

• Bachelor’s Degree or equivalent required.
• 5+ years authoring, editing, and executing validation docs.
• Experience with packaging equipment/lines preferred.
• Experience in pharmaceutical, medical device, or regulated packaging is a plus.
• Proficiency with PC and Microsoft Office tools.
• Outgoing personality with clear, concise communication.
• Strong teamwork and problem-solving abilities.
• GMP and Good Documentation Practice training (may be completed at onboarding).
• Intermediate Word and basic Excel/PowerPoint skills.

Responsibilities

• Author, edit, and execute technical commissioning, qualification, and validation documentation for standard equipment/systems/software and processes as part of the project team.
• Run test scripts and document results.
• Adhere to project schedules for all assigned activities.
• Maintain clear, detailed qualification and validation records.
• Read schematics to identify, locate, and test sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment.

Skills

Communication

Teamwork

Detail-oriented

Problem solving

Time management

Education

Bachelor's degree or equivalent

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job 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

Senior Validation / Senior 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


• Reading technical schematics to identify, locate, and test photo sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment

Requirements:

• Bachelor’s Degree or equivalent required


• 5+ years of experience authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software,


• Prior experience supporting validation, qualification, or testing activities for packaging equipment or packaging lines preferred


• Experience working in or supporting pharmaceutical, medical device, combination product, or regulated packaging operations is a plus


• 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 training (may be completed at onboarding)


• 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

*Verista is an equal opportunity employer.

National (US) Range

$78,925—$128,960 USD

Benefits

• 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