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QC Associate

US - Rhode Island - West Greenwich💼 Full-time💰 $62,572–$84,656🗓 2026-09-29

Core

Perform microbiology and analytical testing, sample handling, and equipment operation in a GMP manufacturing environment to support patient care.

Role type

Associate Quality Control (QC) for Manufacturing

Builds

Biologics and small molecule medicines for oncology, inflammation, general medicine, and rare diseases

Domain

Biotechnology / Pharmaceutical Manufacturing

Required skills

Microbiology testing, Analytical testing, GMP compliance, Sample handling, Equipment operation, Data review, Laboratory documentation, Clean room procedures

Preferred skills

Bioburden testing, Endotoxin testing, LIMS proficiency, Lean Manufacturing, 5S, Project management

Technologies

LIMS, LMES, CIMS, Trackwise

Responsibilities

Perform sample collection and handling for GMP operations; Execute microbiological and analytical tests (bioburden, endotoxin, TOC, conductivity); Operate automated sampling systems and specialized lab equipment; Generate accurate laboratory documentation; Participate in lab investigations and audits; Maintain training compliance and safety guidelines

Seniority

Entry-level to Mid-level, hands-on IC

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