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QA and QC Specialist

Sanford, NC, us💼 Full-time🗓 2026-09-24 → 2026-09-26

Core

Provide Quality Assurance oversight of Quality Control activities, including method validation, equipment qualification, and deviation investigations.

Role type

QA/QC Specialist

Builds

Validated QC methods, qualified equipment, and compliant process control documents for biotech/pharmaceutical clients.

Domain

Biotechnology / Pharmaceutical Manufacturing

Deliverable

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

Required skills

GMP compliance, Method Transfer Validation, Investigation management, Change Control authoring, Equipment Qualification, HPLC testing, GC testing, raw materials testing

Preferred skills

Pharmacopoeia experience

Responsibilities

Review and approve QC method validation and equipment qualification protocols; Support evaluation and resolution of QC deviations; Contribute to process improvement initiatives.

Seniority

Mid-level, hands-on IC

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