Spvr Quality Control

RENSSELAER, USFull-time$79k–$129k2026-10-23 → 2026-11-10

Core

Supervise QC staff and oversee daily operations of Drug Product Packaging and Medical Device Components testing to support testing and release.

Role type

QC Supervisor (Life Sciences)

Builds

Drug Product Packaging and Medical Device Components

Domain

Pharmaceutical / Biotechnology

Required skills

Supervisory/leadership experience, GMP environment experience, cGMP regulations knowledge, SOP writing, lab investigation, personnel management

Preferred skills

MS in Life Sciences, 5+ years progressive experience in pharma/biotech

Technologies

cGMP, SOPs

Responsibilities

Supervises QC staff and distributes workload, Reviews study protocols and reports, Ensures compliance with cGMP regulations and SOPs, Organizes lab investigation and assay troubleshooting, Writes and revises SOPs, methods, protocols, and reports, Supports internal and regulatory audits, Ensures personnel receive proper and prompt training

Seniority

Mid-level Supervisor

About Regeneron

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regu