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QA Specialist Record Review

Limerick💼 Full-time💰 $46,200–$46,200🗓 2026-07-15 → 2026-07-30

Core

Reviewing and approving manufacturing records, batch sheets, electronic batch records, and product changeover documentation to ensure quality compliance.

Role type

QA Specialist Record Review

Builds

Manufacturing records and batch documentation

Domain

Pharmaceutical manufacturing

Deliverable

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

Required skills

attention to detail, organizational skills, ability to learn computerized systems, ability to prioritize multiple tasks

Preferred skills

training and mentorship capabilities, cross-functional communication

Technologies

computerised systems

Responsibilities

Reviewing and approving manufacturing records and batch sheets, participating in shift huddles to provide QA observations, representing QA in support of deviations and change controls, participating in internal and regulatory audits

Seniority

Mid-level, hands-on IC

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