Senior CQV Engineer: Field Startup & Qualification Expert

Verista; Bloomington (IN); On-site; USD 79,000 - 123,000; Full time

Benefits offered by this job

Life Insurance

Short-Term Disability

Long-Term Disability

Health Savings Account (HSA)

Paid Time Off

Tuition Reimbursement

Parental Leave

Employee Referral Program

Job summary

Verista, located in Bloomington, IN, seeks a CQV Engineer to support equipment commissioning and qualification within regulated life sciences environments. The role requires strong CQV lifecycle experience and hands-on field support to ensure successful startup, validation, and documentation.

You will collaborate with vendors and cross-functional teams to review drawings, write URS/IQ/OQ/PQ protocols, and maintain cGMP-compliant records.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or related field.
• 5+ years in engineering, commissioning, qualification, or equipment implementation in regulated environments.
• Experience with CQV lifecycle including FAT, SAT, IQ/OQ/PQ.
• Ability to read engineering drawings and process documentation.
• Strong communication and project coordination skills.
• Ability to work with vendors and cross-functional teams.

Responsibilities

• Provide engineering and CQV support for equipment and systems.
• Review drawings, specifications, datasheets, electrical drawings, and vendor docs.
• Coordinate with vendors, Engineering, Manufacturing, Automation, Quality and other stakeholders.
• Support and execute commissioning, startup, testing, and qualification activities.
• Author and revise CQV documents (URS, protocols, IQ/OQ/PQ, deviations).
• Manage assigned CQV activities to project schedules and report risks.
• Hands-on field support during installation, startup, qualification.
• Investigate and resolve technical issues during commissioning.

Skills

CQV Engineering

P&ID Reading

Documentation

Project Coordination

Vendor Interaction

CQV Lifecycle

cGMP Knowledge

Education

Bachelor’s degree in Engineering or Life Sciences

Tools

Excel

CAD/P&ID Tools

Document Management Systems

Job description

Verista, located in Bloomington, IN, seeks a CQV Engineer to support equipment commissioning and qualification within regulated life sciences environments. The role requires strong CQV lifecycle experience and hands-on field support to ensure successful startup, validation, and documentation.

You will collaborate with vendors and cross-functional teams to review drawings, write URS/IQ/OQ/PQ protocols, and maintain cGMP-compliant records.