CareerPlan

QA Specialist II-Raw Materials Compliance

US - Portsmouth, NHFull-time2026-10-15 → 2026-11-10
On-site · United States

Core

Ensuring quality, compliance, and availability of raw materials for life-changing therapies by reviewing documentation, specifications, and test results.

Role type

Senior IC quality assurance specialist (raw materials compliance)

Builds

Quality release activities and compliance documentation for raw materials

Domain

Life sciences / Pharma manufacturing

Required skills

cGMP knowledge, GDP compliance, technical documentation review, quality system requirements, risk identification, process improvement

Preferred skills

Science or engineering background, cross-functional collaboration, training delivery

Technologies

None stated

Responsibilities

Perform quality release activities for raw materials, review supplier and manufacturer documentation, provide guidance on GDP compliance and inventory controls, partner with cross-functional teams to resolve material issues, support investigations and deviations, identify quality risks and process improvements, develop and deliver training on quality requirements

Seniority

Mid-Senior, hands-on IC