Senior CQV Engineer - Life Sciences Validation

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

Benefits offered by this job

Competitive pay

Health insurance

401(k) with matching

Tuition Reimbursement

Paid time off

Holidays

Parental leave

Disability insurance

Life insurance

Career growth opportunities

Job summary

Verista in Bloomington, IN is seeking a Senior CQV Engineer to support commissioning, qualification, and validation of manufacturing equipment and systems in a regulated life sciences setting. You will review drawings, documents, and participate with vendors and cross-functional teams.

The role requires 5+ years of experience, CQV lifecycle knowledge (FAT/SAT/IQ/OQ/PQ), strong problem-solving and communication, and on-site work in Bloomington.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or related field or equivalent industry experience.
• 5+ years in engineering, commissioning, qualification, validation, or equipment implementation in regulated manufacturing.
• Ability to read engineering drawings, P&IDs, and equipment specs.
• Experience with FAT/SAT/IQ/OQ/PQ and CQV lifecycle activities.
• Strong communication, organizational, and collaboration skills.

Responsibilities

• Provide CQV support for commissioning, qualification, and validation of manufacturing equipment and systems.
• Review drawings, specifications, datasheets, P&IDs, and vendor documentation.
• Coordinate with vendors, Engineering, Manufacturing, Automation, and Quality teams.
• Lead or support startup, commissioning, troubleshooting, and qualification activities.
• Document URS, commissioning protocols, IQ/OQ/PQ reports, risk assessments, and turnover documentation.
• Ensure activities align with project requirements, site procedures, and cGMP expectations.
• Support field installation, startup, testing, and issue resolution.

Skills

CQV lifecycle

Vendor coordination

Documentation drafting

Field support

Problem solving

Education

Bachelor’s degree in Engineering/Life Sciences

Job description

Verista in Bloomington, IN is seeking a Senior CQV Engineer to support commissioning, qualification, and validation of manufacturing equipment and systems in a regulated life sciences setting. You will review drawings, documents, and participate with vendors and cross-functional teams.

The role requires 5+ years of experience, CQV lifecycle knowledge (FAT/SAT/IQ/OQ/PQ), strong problem-solving and communication, and on-site work in Bloomington.