Senior CQV Engineer: Pharma Validation Lead (Onsite Indy)

Verista; Columbus (OH); On-site; USD 70,491 - 109,900; Full time

Benefits offered by this job

Company-paid Life, Short-Term, andLong

Disability Insurance

Medical, Dental & Vision insurances

401(k) Retirement Plan

Paid Time Off

Tuition Reimbursement

Employee Referral Program

Paid Parental Leave and Bereavement

Job summary

Verista is seeking a Senior CQV Engineer to design validation plans, conduct risk assessments, and document qualification activities for pharmaceutical manufacturing.You will lead CQV tasks, write and review validation documentation, and ensure compliance with GMP standards while coordinating with project teams.

The role requires on-site work in the Indianapolis area, 10–50% travel, and 4–6 years of CQV experience. A Bachelor's degree is required.

Qualifications

• Bachelor's degree required or equivalent.
• 4–6 years of demonstrated CQV experience in pharmaceutical manufacturing.
• Ability to mentor and guide less experienced team members; strong client communication.

Responsibilities

• Designing validation plans and executing studies for parameter definition and verification.
• Documenting qualification, validation, and change control activities for audits.
• Authoring and executing commissioning, qualification, validation documents as part of a project team.
• Run test scripts and document results; maintain scheduling discipline.

Skills

Communication

Team leadership

Problem solving

Attention to detail

GMP knowledge

Documentation

Client communication

Mentoring

Team collaboration

Education

Bachelor's degree or equivalent

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Verista is seeking a Senior CQV Engineer to design validation plans, conduct risk assessments, and document qualification activities for pharmaceutical manufacturing.You will lead CQV tasks, write and review validation documentation, and ensure compliance with GMP standards while coordinating with project teams.

The role requires on-site work in the Indianapolis area, 10–50% travel, and 4–6 years of CQV experience. A Bachelor's degree is required.