Operations Quality Shift Lead

As an Operations Quality Shift Lead, you will be responsible for general supervision of the manufacturing inspection and test functions at every stage of the manufacturing process. May supervise inspection and test activities of operators. Performs function failure testing as well as physical defects. This is a shift role on 4 cycles.

Please note any offer of employment for this position isconditional upon the successful completionof a pre-employment medical examination, including drug and alcohol screening, conducted by a medical practitioner designated by the Company

Diabetes Care Kilkenny Key Responsibilities

• Oversees operational implementation of quality assurance strategies and regulations.
• Completes the assessment of potential risks, ensures compliance, and gives recommendations to management.
• Supervises team to ensure quality control aspects of the process are met (laboratories studies, clinical research, testing, operations, raw materials, production, finished product or services).
• Facilitates audits and regulatory inspections.
• Liaises with external vendors, contractors, or suppliers to ensure that their products or services meet the organisation's quality standards.
• Lead a team of Operations Quality engineers.
• Manage functional area's compliance to site and divisional policies and procedures.
• Lead the continuous improvement and effective maintenance of the QMS.
• Subject Matter Expert in use of risk management tools to prioritise activities and justify the effort required.
• Accountable for building and maintaining successful cross functional relationships with departments such as R&D, Technical, Engineering, Operations and Regulatory Affairs in order to achieve all project goals.
• Manage teams Health and Safety within the working environment; highlight opportunities for improvement to EHS performance.
• Act as Lead for the monitoring and compliance of the Quality Management System as it applies to site Operations:
• Lead team in making Quality / Compliance decisions on product during processing, manufacturing, testing, monitoring, and packaging.
• Lead audit readiness in functional area
• Identify and lead projects to enhance and promote the effectiveness and efficiency of the quality system and product quality.
• Champion a "right first time" approach to Quality Records by ensuring accountability for functional responsibilities.

Education and Experience

• A minimum of a NFQ Level 7 Qualification in Science / Engineering or Manufacturing qualification
• Minimum of 4 years' experience in Manufacturing
• Minimum 2 years' experience people management
• Yellow belt qualified desired
• Strong communication and organisation skills
• Strong problem solving
• Experience with GMP/GDP
• ISO13485 experience

What we Offer

• Family health insurance
• Excellent pension scheme
• Life assurance
• Career Development
• Fantastic new facility
• Growing business plus access to many more benefits.

Abbott is an equal opportunities employer.