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QC Specialist, Microbiology

Branchburg, New Jersey

Piper Companies Logo

Job Id:
171353

Job Category:

Job Location:
Branchburg, New Jersey

Security Clearance:
No Clearance

Business Unit:
Piper Companies

Division:
Piper Clinical Solutions

Position Owner:
Karen Pallone

QC Microbiology Consultant (Contract)

Location: Branchburg, NJ (Onsite)

Duration: Contract

Industry: Cell & Gene Therapy / Biopharmaceutical Manufacturing


Piper Companies is seeking an experienced QC Microbiology Consultant to support quality control operations for a leading biotechnology organization focused on advanced therapies. This role will support GMP microbiology testing activities, with a strong emphasis on rapid sterility testing and microbiological quality systems.


Key Responsibilities

  • Perform rapid sterility testing using the BacT/ALERT® system.
  • Execute microbiological testing in accordance with cGMP requirements and internal procedures.
  • Support method validation, qualification, and implementation activities.
  • Perform rapid endotoxin testing
  • Conduct environmental monitoring of classified manufacturing areas.
  • Document laboratory activities accurately and in compliance with GMP documentation practices.
  • Assist with investigations, deviations, and CAPA activities as needed.
  • Collaborate with cross-functional teams to support manufacturing operations and product release timelines.

Required Qualifications

  • Bachelor's degree in Microbiology, Biology, Biochemistry, or a related scientific discipline.
  • Experience working in a GMP pharmaceutical, biotechnology, biologics, or cell and gene therapy environment.
  • Hands-on experience performing rapid sterility testing using BacT/ALERT® (required).
  • Strong understanding of aseptic techniques and microbiological testing principles.
  • Familiarity with GMP documentation and regulatory requirements.

Preferred Qualifications

  • Experience with microbiological method validation or method transfers.
  • Hands-on experience with rapid endotoxin testing
  • Environmental monitoring experience in cleanroom manufacturing environments.
  • Experience with bioburden testing and traditional endotoxin testing.
  • Previous experience supporting biologics, cell therapy, gene therapy, or sterile manufacturing operations.

Ideal Candidate

The ideal candidate has direct experience in QC Microbiology within a GMP environment and is comfortable supporting fast-paced manufacturing operations. Candidates with recent hands-on BacT/ALERT experience and additional expertise in rapid endotoxin testing and environmental monitoring will be highly competitive.

  • If you have the required microbiology experience and are interested in supporting cutting-edge biopharmaceutical manufacturing, we'd love to hear from you.

Compensation:

  • Pay Rate: $85,000-$95,000 on a W2 contract rate; depending on experience
  • Benefits Available: Medical, Dental, Vision, Sick Leave as required by law, and PTO


This job opens for applications on 8/6/2026. Applications for this job will be accepted for at least 30 days from the posting date.  


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