QA Coordinator - Cleanroom Division Location: Birr, Co.
Offaly Company: Elis Department: Cleanroom Days: Monday to Friday About Elis Elis is a leading international provider of cleanroom, textile, hygiene and facility services.
Our Cleanroom Division supports highly regulated industries, including pharmaceutical and biotechnology sectors, delivering high-quality, compliant solutions every day.
Our culture is built on Respect, Integrity, Exemplarity and Responsibility, creating a collaborative environment where employees can grow and succeed.
Benefits We offer a competitive package designed to support our employees' wellbeing and career development: Competitive salary Employee Assistance Programme Full onboarding and structured training Ongoing career development opportunities Access to national and international progression pathways within Elis The Role We are seeking a QA Coordinator to support the Quality Management System (QMS) at our Cleanroom site in Birr.
Working closely with the General Manager and site teams, you will help ensure compliance with regulatory requirements, particularly ISO **** and EN *****.
This role is ideal for someone with experience in cleanroom or pharmaceutical environments who enjoys working in structured, quality-driven operations.
Key Responsibilities Support the implementation, maintenance and continuous improvement of the site Quality Management System.
Ensure compliance across key cleanroom quality processes, including: Gowning procedures Cleaning and contamination control Environmental monitoring Internal auditing CAPA management Deviations and process controls Regulatory and customer inspections Plan and conduct internal audits and support customer and regulatory audits, including closure of non-conformances.
Manage change control activities, validation plans and improvement projects.
Maintain the approved supplier list and ensure suppliers meet required specifications.
Coordinate staff training programmes and maintain accurate training records.
Support quality reporting and management review processes.
About You You will ideally have experience in cleanroom, pharmaceutical, medical device or regulated manufacturing environments, with strong knowledge of: ISO **** and/or EN ***** CAPA, deviation management, change control and validation Internal auditing and regulatory compliance Risk-based quality systems and continuous improvement methodologies You are also: A strong communicator who can work across teams Detail-oriented with excellent organisational skills Proactive in identifying improvements and solving problems Comfortable working in a regulated environment Apply Now If you are motivated by quality, enjoy structured processes, and want to contribute to a high-performing cleanroom operation, we would love to hear from you.
Apply today to join the Elis Cleanroom Division in Birr.