6513 - Senior Validation Engineer / Senior CQV Engineer

Verista; Columbus (OH); On-site; USD 79,000 - 129,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Matching

Paid Time Off

Tuition Reimbursement

Life Insurance

Disability Insurance

Transit Benefits

Parental Leave

Job summary

Verista seeks a Senior Validation / CQV Engineer to author, edit, and execute validation documentation for standard equipment, systems, software, and processes as directed by project leads. You will run test scripts, maintain detailed records, and ensure compliance with GMP and Good Documentation Practice.

Candidates should have a Bachelor's degree, 5+ years in validation, strong communication, teamwork, and proficiency in Word, Excel, and PowerPoint.

Qualifications

• 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.
• Experience supporting validation, qualification, or testing for packaging equipment/lines is a plus.
• Experience in pharmaceutical, medical device, or regulated packaging ops is beneficial.
• Proficiency with PC and Microsoft Office tools.
• Strong communication, teamwork, problem-solving, and time-management skills.
• GMP and Good Documentation Practice training may be completed at onboarding.
• Intermediate skills with WORD (styles, tables, TOCs, track changes), basic Excel and PowerPoint.
• Strong interpersonal and clear communication capabilities.

Responsibilities

• Authoring, editing, and executing validation documentation for equipment, systems, software, and processes as directed by the project leader.
• Running test scripts and documenting results.
• Adhering to project schedules for all assigned activities.
• Maintaining clear, detailed qualification and validation records.
• Reading schematics to identify, locate, and test sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment.

Skills

GMP knowledge

Good Documentation Practice

Microsoft Office

Communication

Teamwork

Problem solving

Time management

Attention to detail

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job 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

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: $78,925 USD - $128,960 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