Onsite Downstream CQV Engineer - 6-Month Contract

Zachary Piper Solutions; Holly Springs (NC); On-site; USD 103,000 - 117,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401K

Job summary

Piper Companies seeks a Downstream CQV Engineer to join a growing biopharmaceutical manufacturing site in Holly Springs, NC for a 6-month onsite contract. The role focuses on commissioning, qualification, and verification of downstream process equipment across multiple buildings in a greenfield-style environment.

Responsibilities include executing IQ/OQ/PQ activities, P&ID walkdowns, DeltaV-related verification, qualification documentation, and on-the-floor problem solving to ensure GMP

Qualifications

• Hands-on experience across IV, OV and PQ; two or more required.
• Experience supporting downstream manufacturing operations such as buffer prep, chromatography, UF, or bulk fill.
• 2–5 years of experience qualifying large-scale manufacturing or utility equipment in a regulated environment.

Responsibilities

• Execute Installation, Operational, and Performance Qualification activities for downstream process equipment and systems.
• Perform field-based verification activities including P&ID walkdowns, system turnover, and equipment checks.
• Support software and automation execution efforts, including Operational Verification tied to DeltaV-controlled systems.
• Author, review, and execute qualification documentation while balancing significant on-the-floor execution.
• Troubleshoot equipment and system issues during qualification and support startup activities across DSM facilities.

Skills

IV

OV

PQ

Tools

DeltaV

Job description

Piper Companies seeks a Downstream CQV Engineer to join a growing biopharmaceutical manufacturing site in Holly Springs, NC for a 6-month onsite contract. The role focuses on commissioning, qualification, and verification of downstream process equipment across multiple buildings in a greenfield-style environment.

Responsibilities include executing IQ/OQ/PQ activities, P&ID walkdowns, DeltaV-related verification, qualification documentation, and on-the-floor problem solving to ensure GMP