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In-Process Quality Assurance (IPQA) Specialist

US - Bend, OR💼 Full-time🗓 2026-07-29 → 2026-09-26

Core

Provide real-time quality oversight of manufacturing operations to ensure product quality, safety, and regulatory compliance for life-changing medicines.

Role type

In-Process Quality Assurance (IPQA) Specialist

Builds

Pharmaceutical and biotechnology manufacturing operations

Domain

Life sciences / Pharmaceutical manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

cGMP knowledge, batch record review, quality event investigation, line clearance verification, material handling oversight, regulatory compliance monitoring

Preferred skills

SAP or similar manufacturing systems familiarity, scientific or engineering degree background

Responsibilities

Monitor manufacturing and packaging activities for compliance, review batch records and production documentation, identify quality events and support investigations, perform line clearances, support material receipt and dispensing activities, partner with production teams to resolve issues, maintain compliant and safe manufacturing environment

Seniority

Mid-level, hands-on IC

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