
Director QA/RA
- Dublin
- Permanent
- Full-time
- Develop and lead the company's QA/RA strategy, ensuring alignment with business goals and regulatory requirements.
- Oversee regulatory submissions and communications with global regulatory bodies including the FDA, EMA, and Notified Bodies.
- Ensure compliance with EU MDR, FDA 21 CFR Part 820, and other applicable regulations.
- Lead the implementation and maintenance of ISO 13485 certified Quality Management System.
- Ensure product development processes comply with IEC 62304 (software lifecycle) and IEC 60601 (electrical safety).
- Manage internal and external audits, CAPAs, and risk management activities.
- Collaborate cross-functionally with R&D, Clinical, and Operations to ensure regulatory and quality requirements are met throughout the product lifecycle.
- Monitor changes in global regulations and standards, and proactively update internal processes.
- Mentor and develop the QA/RA team, fostering a culture of compliance and continuous improvement.
- Bachelor's or Master's degree in Engineering, Life Sciences, or related field.
- Proven years of working experience in QA/RA within the medical device industry.
- Proven experience with FDA submissions (510(k), PMA) and EU MDR compliance.
- Strong knowledge of IEC 62304, IEC 60601, and ISO 14971.
- Experience leading audits and managing QMS under ISO 13485.
- Excellent leadership, communication, and project management skills.
- Ability to work in a fast-paced, innovative environment.
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