QC Coordinator

Summary:

Role Overview

Expanding Pharmaceutical site in Cork requires a highly motivated QC Coordinator with strong experience in pharmaceutical manufacturing to join their team. The QC Co-ordinator is responsible for the line management supervision and technical support for a team of laboratory analysts. With responsibility for the overall operation of the laboratory in compliance with cGMP, environmental and safety requirements.

Responsibilities

• Manage the day-to-day functioning of the QC team and laboratory to ensure efficient operation in compliance with cGMP standards and close liaison with Production, QA and Supply chain.
• Supervision/completion of necessary out-of-specification/expectation investigations and deviation reports
• Monitor training programs for laboratory personnel in order to maintain a high scientific and technical standard within the laboratory.
• Ensure laboratory equipment is well maintained and calibrations are carried out at the designated frequencies.
• Track team metrics and ensure KQI/KPI meet requirements and lead relevant OpEx projects

Requirements

• Previous people management experience
• Ability to problem solve and implement solutions independently in a fast-paced environment
• Scientific undergraduate Degree with 5+ years' experience within a GMP environment

Fastnet has a strict confidentiality policy - please be assured that your details will never be forwarded to any third party without your consent.

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