Quality Control Technician

AS22683

Contract – 11 months

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Reporting into the Quality Control Manager/ Associate Director Quality Control, the Quality Control Technician will be responsible for performing QC assignments for the site’s quality systems, processes and controls. They will be accountable for contributing to ensure that objectives are effectively achieved, consistent with the company’s requirements to ensure compliance, safety & reliable customer supply. They will also respond to operational and business areas, ensuring compliance with cGMP & corporate regulations and support the performance of the site cGMP activities.

Duties:

• Comply with and execute CGMP/GDP in the performance of day-to-day business activities.
• Ensure data integrity principles: Attributable, Legible, Contemporaneous, Original, and Accurate (ALCOA) are adhered to for records and data in day-to-day business activities.
• Liaise with the QC Leads to resolve quality related queries where required
• Ensure that adequate processes and procedures are in place and followed for all Quality activities.
• Provide support to the relevant support functions to ensure manufacturing and release activities, in compliance with applicable procedures, our Company’s Global Policies and Guidelines, regulatory requirements and current Good Manufacturing Practices (cGMP).
• Identify and support compliance initiatives to improve compliance status and overall operational efficiency for batch release at the site.
• Support business critical projects related to the Quality Department.
• Use MPS principles and tools to identify and support continuous improvement by active participation to ensure quality systems and work practices are effective, efficient and ensure compliance and overall operational efficiency for batch and material release at the site where required.
• Provide quality support of controls and procedures for the end to end material and product lifecycle where applicable.
• Assist team members to support the qualification/validation, technical transfers, and commercial operations at the facility where required.
• Supports the Laboratory and team members with day to day activities, as applicable.
• Ensure compliance to regulatory requirements.
• Assist team members with tasks relating to SOP's, deviations, cleaning verification/validation data and other documents as necessary for the Quality and Manufacturing departments where required.
• Contribute to effective writing/revising/rolling out of accurate operational procedures, training materials and maintenance procedures for various Quality related systems