Senior CQV Engineer — Validation & Compliance Lead

Verista; Indianapolis (IN); On-site; USD 70,491 - 109,900; Full time

Benefits offered by this job

Competitive pay

Life Insurance

Medical, Dental, Vision

401(k) matching

Paid Time Off

Tuition Reimbursement

Job summary

Verista is seeking a Senior CQV Engineer to join our Indianapolis team. The role involves designing validation plans, performing risk assessments, and maintaining thorough qualification documentation.

You will lead CQV activities for pharma manufacturing, ensure compliance with GMP and GDp, and collaborate with project teams to meet schedules. The candidate should have 4–6 years of relevant CQV experience, strong communication skills, and the ability to mentor colleagues in a fast-paced, on-site

Qualifications

• Bachelor’s degree required or equivalent in a related field.
• Demonstrated 4–6 years of role-relevant experience.
• Experience leading CQV activities in pharmaceutical manufacturing.
• Proficient in GMP and Good Documentation Practice.

Responsibilities

• Designing validation plans for equipment, systems, and software.
• Maintaining detailed qualification and validation records for audits.
• Executing engineering studies to define and verify critical process parameters.
• Authoring CQV documentation and reviewing test results.
• Performing UI testing, software verification, and alarm testing on automated systems.
• Collaborating with project teams to meet schedules and quality targets.

Skills

CQV Leadership

Client Communication

GMP Knowledge

Attention to Detail

Time Management

Team Collaboration

Mentoring

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Word

Excel

PowerPoint

Job description

Verista is seeking a Senior CQV Engineer to join our Indianapolis team. The role involves designing validation plans, performing risk assessments, and maintaining thorough qualification documentation.

You will lead CQV activities for pharma manufacturing, ensure compliance with GMP and GDp, and collaborate with project teams to meet schedules. The candidate should have 4–6 years of relevant CQV experience, strong communication skills, and the ability to mentor colleagues in a fast-paced, on-site