CareerPlanSign in

QA Specialist (Contract)

Hybrid💼 Contract💰 $49–$49🗓 2026-08-04 → 2026-09-26

Core

Perform quality functions including equipment onboarding, record reviews, nonconformance investigations, CAPAs, change controls, deviations, and internal audits for pharmaceutical/biologic manufacturing.

Role type

Quality Assurance Specialist (Contract)

Builds

Ensures compliance with cGMP and regulatory standards in biotech manufacturing processes.

Domain

Biotechnology / Pharmaceutical Manufacturing

Deliverable

client delivery

Required skills

cGMP knowledge, regulatory standards understanding, nonconformance investigation, CAPA management, change control, deviation management, internal auditing, data collection and analysis

Preferred skills

Life Sciences background, Quality Assurance certificate

Technologies

None stated

Responsibilities

Equipment onboarding and logbook management, batch and calibration record review, Nonconformance investigation management, Deviations handling, CAPAs management, Change Control management, Internal audits

Seniority

Mid-level, hands-on IC

Sourced via greenhouse · Listed on CareerPlan, which tracks 70,000+ jobs from 20+ sources.