QC Analyst - Ireland - CPL Healthcare

Description

QC Analyst- Evening Shift

My client, a global pharmaceutical company, who specialises in developing, registering and manufacturing of both human generic and veterinary pharmaceutical products, seeks to hire a new QC Analyst.

This role will suit someone with a 3 rd level education in chemistry and as a Quality Control Analyst, who wishes to grow their career in a world-renowned organisation.

This is a permanent position, based on site at their headquarters in East Co. Galway.

Responsibilities

• Understand how to demonstrate technical proficiency in the following areas: HPLC, IR, UV, dissolution & physical testing.
• Ensuring that laboratory always meets GLP/GMP standards.
• To maintain all laboratory logbooks and document all records relating to Quality Control and store accordingly.
• Maintain and follow all relevant Standard Operating Procedures (SOP's).
• Provide a full analysis of contract manufactured products in accordance with customer specifications.
• Full analysis of finished products, including tablets, boluses and veterinary drenches. This to be completed using appropriate analytical techniques.
• Provide samples for external analysis when requested.
• Participating in internal/External Audits.
• Support the laboratory testing schedule to achieve an efficient QC system and Customer Service level of >95%.
• Follow up on Corrective Actions.
• Responsible for communication with external suppliers and vendors, in relation to QC consumables.

Requirements

• 3rd level Qualification in a chemistry-based discipline.
• 4+ years' experience as a QC Analyst.
• Knowledge of US FDA guidelines.
• Experience working in a pharmaceutical cGLP environment.

For more information, please contact

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