QC Microbiology Jobs at Minaris Advanced Therapies | BS Life Science Graduates Apply Now
Start your career in cutting-edge science with Minaris Advanced Therapies, a global leader in cell and gene therapy development and manufacturing. As a QC Microbiology Analyst I in Allendale, NJ, you’ll play a key role in environmental monitoring and quality control, ensuring life-saving therapies meet the highest standards. This is your opportunity to contribute directly to transformative treatments that change lives.
- Job Position: QC Microbiology Analyst I
- Location: Allendale, NJ
About the Company:
Minaris Advanced Therapies is a leading global contract development and manufacturing organization specializing in cell and gene therapies. With over 1,000 experts across North America, Europe, and Asia, Minaris partners with innovators to bring advanced treatments from concept to market. Their mission is to create hope for patients by turning breakthrough science into real-world solutions, backed by a culture of innovation, collaboration, and patient impact.
Job Description:
The QC Microbiology Analyst I supports clinical and commercial production by conducting environmental monitoring and quality control activities to ensure product quality. This role ensures controlled environments meet strict regulatory and quality standards through monitoring, testing, and maintaining lab compliance under cGMP and GDP guidelines.
Key Responsibilities:
- Conduct environmental monitoring in controlled rooms, encompassing both viable and non-viable monitoring, air and surface sampling, personnel monitoring, and equipment monitoring.
- Conduct plate reads, incubations, and EM data review/trending.
- Maintain and calibrate equipment; monitor systems in Vaisala.
- Initiate quality events in Veeva and collaborate with other departments.
- Support routine laboratory testing and inventory management.
- Ship test samples/equipment to contract labs.
- Ensure audit readiness and follow Good Laboratory Practices.
- Complete documentation per SOPs in compliance with cGMP and GDP.
Qualifications:
- BA/BS in a science or relevant field, or equivalent experience.
- 0–2 years of experience; experience in environmental monitoring or biopharma preferred.
- Proficient in Microsoft Office, MODA/LIMS.
- Strong attention to detail, communication skills, and adaptability to changing schedules.
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