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QC Lab Supervisor - Days

Sligo, SO, ie💼 Full-time🗓 2026-08-31 → 2026-09-25

Core

Lead a team of laboratory analysts to ensure raw materials, in-process samples, and finished products are tested to the highest quality standards, on schedule, and in compliance with GMP and regulatory requirements.

Role type

Senior IC QC Lab Supervisor

Builds

Production quality data and compliant finished products

Domain

Pharmaceutical manufacturing / Quality Control

Deliverable

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

Required skills

HPLC, GC, LCMS, GCMS, titration, identification methods, GMP compliance, data integrity, root cause analysis, CAPA, team leadership, analytical investigations

Preferred skills

Product or method transfer experience

Technologies

HPLC, GC, LCMS, GCMS

Responsibilities

Lead, coach, and develop a team of QC analysts; Ensure compliance with GMP, Data Integrity, HPRA/FDA, and internal quality requirements; Oversee laboratory testing activities and ensure adherence to testing schedules; Drive continuous improvement, Right First Time (RFT), and operational excellence initiatives; Lead analytical investigations, OOS/OOT events, root cause analysis, and CAPA activities; Support laboratory inspections, audits, product transfers, and project work; Maintain laboratory documentation, procedures, training records, and equipment compliance.

Seniority

Senior, hands-on IC

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