22683-QC Technician-Carlow Contractor

This is an 11-month contract and is a 2 shift cycle. It is an onsite role.

Purpose 

• Performs QC assignments for Carlow quality systems, processes and controls.
• Accountable for contribution to ensure that objectives are effectively achieved, consistent with Company requirements to ensure compliance, safety & reliable customer supply.
• Responds to Operational and business area’s, ensuring compliance with cGMP and corporate regulations.
• Support the performance of the site cGMP activities.

Responsibilities 

• 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.
• Attend and successfully complete applicable CGMP training.
• Escalate any potential violation of CGMP and/or other concerns which may affect the safety, efficacy, quality, or purity of MMD human health products.
• Work collaboratively to ensure a safe and compliant culture in Carlow.
• Participate in driving a high performing & inclusive culture, stimulating personal growth & development.
• May be required to perform other duties as assigned.
• 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.
• Where required work shift patterns in line with manufacturing operations to ensure Quality operations (including testing, delivery and or oversight) as required as per business needs & if needed.
• 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).
• Develop and maintain effective cross-functional relationships with other departments and support functions to ensure that the process for the manufacturing, testing and release of vaccine and biologic products are in compliance with cGMP and the associated regulatory requirements.
• 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.
• Responds to standard requests and communication processes to allow the flow of appropriate information between departments.
• 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..
• Support in resolving routine potential quality issues.
• 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.

Qualifications

• Leaving Certificate or other relevant experience.