Downstream CQV Engineer - 175487

ZP Group

Holly Springs (NC)

On-site

USD 103,000 - 117,000

Part time

4 days ago
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Benefits offered by this job

Medical Benefits
Dental Benefits
Vision Benefits
401K Matching

Job summary

Piper Companies is seeking a Downstream CQV Engineer to join a growing life sciences manufacturing organization for a 6-month contract onsite in Holly Springs, NC. The role focuses on commissioning, qualification, and verification across multiple new and existing facilities in a greenfield-style biopharmaceutical setting.

You will perform IQ/OQ/PQ activities for downstream equipment, support DeltaV-based automation, and author qualification documentation while balancing hands-on field execution.

Qualifications

  • Experience across IV/OV/PQ in downstream manufacturing
  • Background in downstream processes such as chromatography, UF, or fill/dispense
  • 2–5 years' experience qualifying large-scale equipment in regulated environments
  • Exposure to DeltaV systems or startup projects is desirable

Responsibilities

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

Skills

IV
OV
PQ

Tools

DeltaV

Job description

Piper Companies is seeking a Downstream CQV Engineer to join a growing life sciences manufacturing organization for a 6-month contract onsite role supporting large-scale downstream operations based out of Holly Springs, NC. The Downstream CQV Engineer will play a key role in commissioning, qualification, and verification activities across multiple new and existing manufacturing buildings within a greenfield-style environment in the biopharmaceutical industry.

Responsibilities of the Downstream CQV Engineer include:
  • 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.
Qualifications for the Downstream CQV Engineer include:
  • Hands-on experience across at least two of the following: IV, OV, and PQ (IV and OV strongly preferred).
  • Background supporting downstream manufacturing operations such as buffer preparation, chromatography, UF, or bulk fill and dispense.
  • 2–5 years of experience qualifying large-scale manufacturing or utility equipment in a regulated environment.
  • Strong field execution experience with the ability to learn and apply documentation standards and best practices.
  • Exposure to DeltaV systems, troubleshooting activities, or greenfield/start-up projects is highly desirable.
Compensation for the Downstream CQV Engineer:

Salary Range: $75-$85/hr (USD)

Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

This job opens for applications on 9/30/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: CQV, commissioning, qualification, validation, IV, OV, PQ, downstream manufacturing, buffer preparation, chromatography, ultrafiltration, UF, DeltaV, automation, P&ID walkdowns, field verification, large-scale equipment, utilities, greenfield projects, biopharmaceutical manufacturing, GMP, Kneat, documentation, troubleshooting, startup support, process engineering, regulated manufacturing.

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