QC Specialist, Microbiology
Branchburg, New Jersey
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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