Onsite Downstream CQV Engineer – Greenfield Biologics

Zachary Piper Solutions

Holly Springs (NC)

On-site

USD 110,000 - 130,000

Full time

4 days ago
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Benefits offered by this job

Health insurance
Vision and Dental
Paid time off

Job summary

Piper Companies in Holly Springs, NC, is seeking a Downstream CQV Engineer to support a greenfield biologics manufacturing facility. This onsite, full-time role targets professionals with 2–5 years of CQV experience, focusing on IQ/OQ/PQ execution and field activity on the manufacturing floor during startup and qualification.

The ideal candidate will work closely with engineering, manufacturing, and quality teams to ensure smooth handover from construction to qualification, while maintaining GMP

Qualifications

  • 2-5 years of CQV experience in pharma/biotech
  • Hands-on execution of IQ/OQ/PQ protocols
  • Strong field execution on manufacturing floor

Responsibilities

  • Execute commissioning, qualification, and validation activities for downstream process equipment and supporting systems in a biologics manufacturing environment.
  • Perform IQ, OQ, and PQ protocol execution, documentation, and troubleshooting.
  • Collaborate with engineering, manufacturing, quality, and project teams to transition systems from construction to qualification.
  • Support field verification, walkdowns, punch list resolution, and turnover package reviews during startup and commissioning.
  • Ensure CQV activities comply with GMP requirements, site procedures, and regulatory expectations.

Job description

Piper Companies in Holly Springs, NC, is seeking a Downstream CQV Engineer to support a greenfield biologics manufacturing facility. This onsite, full-time role targets professionals with 2–5 years of CQV experience, focusing on IQ/OQ/PQ execution and field activity on the manufacturing floor during startup and qualification.

The ideal candidate will work closely with engineering, manufacturing, and quality teams to ensure smooth handover from construction to qualification, while maintaining GMP

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