6348 - Validation Engineer / CQV Engineer

Veristainc; Columbus (OH); On-site; USD 70,000 - 118,000; Full time

Benefits offered by this job

Competitive pay & incentives

Health & life insurance

Tuition reimbursement

401(k) with match

Paid time off & holidays

Job summary

Verista is seeking a Validation/CQV Engineer to join our team in the United States. The role involves authoring and executing validation documentation for equipment, systems, and software, while adhering to project schedules and maintaining meticulous records.

Strong communication and teamwork are essential, with a focus on GMP practices and Good Documentation. The ideal candidate holds a Bachelor’s degree or equivalent and has experience in pharmaceutical, medical device, or regulated packaging

Qualifications

• Bachelor’s Degree or equivalent required.
• Experience supporting validation, qualification, or testing activities for packaging equipment or packaging lines preferred.
• Experience in pharmaceutical, medical device, or regulated packaging operations is a plus.
• Proficiency with PC and Microsoft Office tools.
• Strong communication and teamwork abilities; detail-oriented and organized.

Responsibilities

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

Skills

Communication

Teamwork

Problem solving

Time management

Detail oriented

GMP training

Education

Bachelor's Degree

Tools

Word

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

Validation/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


• 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

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job‑related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

Verista is an equal opportunity employer.

National (US) Range

$70,491 — $118,062 USD

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