Downstream CQV Engineer - 175521

Responsibilities: of the Downstream CQV Engineer include: • Execute commissioning, qualification, and validation activities for downstream process equipment and supporting systems within a biologics manufacturing environment. • Perform Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocol execution, documentation, and troubleshooting. • Partner closely with engineering, manufacturing, quality, and project teams to ensure systems are transitioned effectively from construction through qualification. • Support field verification activities, walkdowns, punch list resolution, and turnover package reviews during startup and commissioning phases. • Ensure all CQV activities are conducted in compliance with GMP requirements, site procedures, and regulatory expectations. Requirements of the Downstream CQV Engineer include: • 2-5 years of experience supporting CQV activities within pharmaceutical, biotech, or life sciences manufacturing environments. • Hands-on experience executing IQ, OQ, and PQ protocols for process equipment, utilities, or manufacturing systems. • Strong field execution background with the ability to work directly on the manufacturing floor during startup and qualification activities. • Familiarity with GMP regulations, validation lifecycle principles, and commissioning best practices. • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline. Compensation: for the Downstream CQV Engineer include: • $110,000 - $130,000 annually • Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law. • Opportunity to support a large-scale greenfield biologics manufacturing startup project. • This job opens for applications on 10/2/2026. Applications for this job will be accepted for at least 30 days from the posting date.