CareerPlan

Associate II, Quality Control Materials

Research Triangle Park, NC, USFull-time$57k–$74k2026-11-06 → 2026-11-10

Core

Perform raw material sampling, inspections, release testing, cleaning validation, and utility monitoring to support material release decisions in Biogen manufacturing operations.

Role type

Associate II Quality Control Materials (GMP)

Builds

Raw material and utility systems for Biogen manufacturing

Domain

Biotechnology / Pharmaceutical Manufacturing

Required skills

GMP compliance, laboratory techniques, data review, investigation protocols, deviation management, physical mobility, PPE usage

Preferred skills

GMP environment experience, raw materials familiarity, SDS compliance

Technologies

Laboratory equipment, GMP/GLP systems

Responsibilities

Perform raw material sampling, inspections, release testing, cleaning validation, and utility monitoring; Author investigation protocols, change control requests, and validation documentation; Review laboratory data for accuracy and compliance; Support investigations and corrective actions; Maintain laboratory systems for data integrity; Partner with cross-functional teams to support production schedules.

Seniority

Entry Level, hands-on IC