Quality Control Manager

Overview

My Client are a global materials science and digital identification solutions company with a presence in 50 countries. They manufacture different types of labelling used in various industries such as pharmaceuticals, food and healthcare. They are expanding their team in Longford and looking to add a Quality Control Manager. This is a full‑time permanent position with hybrid working.

Responsibilities

• You will manage the quality function by providing work direction for quality engineers and inspectors and interacting regularly with engineering, manufacturing, and service functions to establish quality standards for raw materials, work in process, and finished products.
• Formulate a strategy to foster a high‑performance culture with quality right the first time suitable for a world‑class medical device contract and legal manufacturer.
• Coach and develop staff who support the quality function during the manufacturing process and drive a culture of quality awareness.
• Drive improvements to the quality system that ensures its suitability, adequacy, and effectiveness.
• Understand and ensure compliance with cGMP, ISO 13485, and FDA 21 CFR Part 820 regulations.
• Work closely with commercial and operations to build value with top 10 key accounts and engage with customer quality representatives directly to implement short, medium, and long‑term innovation and improvement plans.

Required

• Bachelor’s degree in Engineering or a scientific related field.
• A minimum of 4 years of experience in the medical device or pharmaceutical industry with at least 3 years of experience in regulatory compliance and quality systems.
• At least 4 years of experience in managing a team.
• Thorough knowledge of ISO 13485 and 21 CFR Part 820.
• Strong written and verbal communication skills alongside strong presentation skills, with the ability to effectively work with various functions and levels within the organization.