Compliance and Regulatory Affairs Specialist

2 weeks ago


Sligo, Sligo, Ireland TN Ireland Full time
Responsibilities and Requirements

The successful candidate will be responsible for ensuring compliance with quality standards and regulatory requirements, leading a dedicated team of quality professionals. To be considered for this role, applicants must have a Bachelor's degree in science/engineering and 5 years' experience in the healthcare/pharmaceutical industry. A Master's degree is preferred. Ideal candidates should have 6 years in Manufacturing/QA/R&D in relevant industries and 3 years in quality management.

A strong understanding of statistical quality systems, cGMP, and regulatory requirements is essential. Strong leadership, communication, and interpersonal skills are necessary. High attention to detail, commitment to quality, and integrity are also required.

About the Team

The Medical Device Quality team is responsible for ensuring compliance with quality standards and regulatory requirements. The successful candidate will join a dynamic team that is committed to delivering high-quality products and services.



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