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Lead QA Tech Technician (8hr days, Monday-Friday)

Greenville, North Carolina, USA💼 Full-time🗓 2026-09-11 → 2026-09-26

Core

Lead quality oversight of GMP manufacturing operations, including aseptic processing, for sterile injectable and oral solid dose drug products.

Role type

Lead QA Technician (Pharmaceutical Manufacturing)

Builds

Sterile injectable and oral solid dose drug products

Domain

Pharmaceutical manufacturing / GMP compliance

Deliverable

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

Required skills

Batch record review, deviation investigations, CAPA management, aseptic manufacturing controls, cleanroom operations, gowning practices, regulatory inspection support, data integrity standards

Preferred skills

Chemistry/Pharmacy/Biology/Biotechnology background, project management, continuous improvement initiatives

Technologies

TrackWise, Documentum, Microsoft Office

Responsibilities

Provide independent quality oversight of GMP manufacturing operations, lead batch record review, lead deviation investigations and root cause analysis, support regulatory inspections and audits, mentor QA Technicians, ensure compliance with site procedures and data integrity standards

Seniority

Senior, hands-on IC with team guidance

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