2nd Shift QC Microbiology Supervisor

Regulatory Jobs; City of Rensselaer (NY); Sur place; USD 79 000 - 129 000; Plein temps

Résumé du poste

Regeneron is seeking a 2nd shift Quality Control Supervisor focused on Microbiology in Rensselaer, NY. The role ensures daily QC operations support pharmaceutical microbiology testing, environmental monitoring, and product release readiness to help keep medicines safe and effective.

You will coordinate testing in the QC lab, review results, lead investigations, support audits, and manage a small team, while ensuring adherence to cGMP and safety standards on a Tuesday–Saturday schedule.

Qualifications

• BS/BA in Life Sciences or related field with 5+ years of relevant experience preferred in pharmaceutical microbiology
• Must be able to work 2nd shift Tuesday- Saturday, 2 PM - 10:30 PM
• Supervisory/leadership experience required

Responsabilités

• Coordinate testing and monitoring within the QC lab and manufacturing facility.
• Review test results, procedures, protocols, and quality system records.
• Attend cross-functional meetings to stay informed of business needs.
• Organize lab investigations and assay troubleshooting as needed.
• Support internal and regulatory audits.
• Ensure safety and current Good Manufacturing Practice standards are maintained.
• Execute personnel management functions including performance evaluations and scheduling time off.
• Communicate effectively with management on complex matters; support laboratory management in mid to long range team goals.
• Drive and manage projects within the group.
• Coach team members in troubleshooting microbiology methods, Environmental Monitoring, aseptic techniques and equipment.

Connaissances

Quality Control

Microbiology

Leadership

Shift Work

Formation

BS/BA Life Sciences or related field

Description du poste

Regeneron is seeking a 2nd shift Quality Control Supervisor focused on Microbiology in Rensselaer, NY. The role ensures daily QC operations support pharmaceutical microbiology testing, environmental monitoring, and product release readiness to help keep medicines safe and effective.

You will coordinate testing in the QC lab, review results, lead investigations, support audits, and manage a small team, while ensuring adherence to cGMP and safety standards on a Tuesday–Saturday schedule.