CareerPlan

Quality Control Associate

US - Vacaville, CAFull-time$78k2026-11-11 → 2026-11-12
On-site · United States

Core

Perform specialized technical tasks in laboratory testing and deviation management to manufacture medicines to the highest quality and safety standards.

Role type

Quality Control Associate (Laboratory/Deviation Management)

Builds

Medicines manufactured to cGMP standards

Domain

Life Sciences / Pharmaceutical Manufacturing

Required skills

Laboratory testing, Deviation management, cGMP compliance, Cell based assays, ELISA, Potency methods

Preferred skills

Effective communication, Information analysis, Adaptability, Prioritization

Technologies

cGMP, EHS, Lonza standards

Responsibilities

Perform operational roles such as laboratory testing; Execute duties in alignment with Quality Control policies and cGMP requirements; Conduct work to meet customer commitments.

Seniority

Mid-Senior level (5-10 years experience)