QC Microbiology Co-op Job at WuXi Biologics, Cranbury NJ – Apply Now!
Looking for a hands-on learning opportunity in biotech? WuXi Biologics is offering a QC Associate Co-op position in Microbiology Testing at its Cranbury, NJ facility. This role is ideal for undergraduate or graduate students in Biology, Chemistry, Pharmacy, or Chemical Engineering. Gain real-world experience in microbiological testing, GMP compliance, and quality control practices while working with a global leader in biologics development and manufacturing.
About WuXi Biologics
WuXi Biologics is a global Contract Research, Development, and Manufacturing Organization (CRDMO) offering end-to-end solutions to help companies discover, develop, and manufacture biologics. With cutting-edge facilities and a global footprint, WuXi empowers the pharmaceutical and biotech industries to accelerate their innovation pipeline. Known for its commitment to quality, compliance, and scientific excellence, WuXi Biologics is an ideal workplace for early-career professionals looking to learn and grow.
Job Details:ย
Job Title: QC Associate (Co-op) – Microbiology Testing (4888)
Requisition ID: 4888
Location: Cranbury, NJ – United States
Job Description
Job Summary
The QC Micro Associate (Co-op) is responsible for the quality and on-time completion of micro tests, microbiology laboratory inventory management to the various testing sections. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates good oral and written communication skills and actively contributes to timely training, report generation and good GMP documentation and archival.
Responsibilities
- Understand GMP and follow the instructions on the documents.
- Perform micro-related testing, including but not limited to bioburden, pH, growth promotion, endotoxin, conductivity, TOC, nitrate, CCIT, etc.
- Support reagents/consumables inventory management to ensure consistent QC Microbiology operation needs.
- Record and organize experimental data in accordance with “Good Document Management Practices” to ensure data integrity.
- Ensure compliance with training, preparation, documentation, and general lab maintenance requirements for Industry Standards and/or Regulations.
- Maintains laboratory logbooks and worksheets for QC tasks as required.
- Able to work on weekends when needed.
- Support shift work when needed.
- Any other duties assigned by the supervisor (when applicable).
Qualifications
Technical Skills / Knowledge:
- The candidate must possess a willingness to learn about analytical and QC operations in the pharmaceutical industry, understand current regulations and industry trends related to biologics product development, characterization, and manufacturing testing requirements, including cGMP, ICH, EMA, FDA, and other global compendia regulations and guidance.
- Basic familiarity with analytical instruments and methodologies, such as a TOC and a conductivity meter, is preferred but not mandatory.
- Familiar with Office software such as Word, Excel, and PowerPoint.
- Ability to understand technical data.
Problem Solving:
Be able to raise issues immediately to the supervisor and work with the supervisor when in doubt.
Communication Skills:
Proficiency in English is required. Good communication skills (verbal, written, and presentation skills). Effectively exchange information or discuss clearly framed issues or ideas with colleagues.
Education and Experience:
Undergraduate or graduate students majoring in biology or related majors.
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