CQV Engineer

Initial 6-month contract role supporting a large-scale CAPEX project for a global pharmaceutical manufacturing organization in Ohio.

About the role

Contribute to the commissioning, qualification, and startup of a brand-new manufacturing facility on the East Coast of the United States. This opportunity is part of continued organizational growth and significant investment across capital programs.

Responsibilities

• Support commissioning, qualification, and startup activities for chromatography and column packing systems.
• Generate, review, and execute CQV lifecycle documentation including DQ, RTM, QRA, FAT, SAT, IOC, IOQ, and Final Reports.
• Review design deliverables including P&IDs, drawings, specifications, datasheets, and vendor documentation.
• Support vendor package reviews and equipment acceptance activities.

Requirements

• Bachelor's Degree in Engineering, Life Sciences, or related technical discipline (preferred).
• Extensive experience within CQV, Validation, Commissioning, Qualification, or related pharmaceutical engineering functions.
• Demonstrated hands-on experience with chromatography column packing activities.
• Strong understanding of downstream processing systems and equipment.