Quality Assurance Engineer - County Roscommon, Ireland - Cpl

Description

My client is a leading medical device contract manufacturer, specialising in innovative solutions for various medical devices. An exciting opportunity has arisen for a Quality Assurance Engineer to ensure compliance with regulatory requirements and industry standards in all manufacturing processes.

Responsibilities:

· Develop and maintain quality assurance policies and procedures.

· Conduct audits and inspections to ensure compliance with regulatory requirements (e.g., FDA QSR, ISO

· Review and approve documentation related to manufacturing processes, including SOPs, batch records, and validation protocols.

· Investigate and resolve quality issues, implementing corrective and preventive actions as needed.

· Provide training and support to manufacturing teams on quality-related processes and procedures.

Requirements:

· Bachelor's degree in in Quality Assurance or similar discipline.

· 3+ years of experience in quality assurance, preferably in medical device manufacturing.

· Proficient with Syspro, Minitab & Lotus Notes, is desirable.

· Strong understanding of regulatory requirements and quality management systems.

· Experience with auditing, documentation review, and CAPA processes.

· Excellent communication and problem-solving skills.

If you are looking for a role where you'll have the opportunity to work with products at the forefront of medical device technology, and opportunities for professional growth, please send on your CV to today

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