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We are looking for a highly organised and proactive Quality Assurance Regulatory Affairs (QARA) Coordinator to join our team at Perspectum. This is an exciting opportunity to play a key role in supporting the administration of quality and regulatory activities that ensure our continued compliance within a medical device environment.
Job Responsibility:
Develop and deliver QARA training and inductions on core QMS processes, procedures, and requirements
Create and maintain training materials, ensuring accurate and up-to-date training records across the business
Provide administrative support to ensure regulatory affairs (RA) activities and timelines are effectively managed
Support the development, implementation, and continuous improvement of QARA strategies and the QMS
Ensure compliance with local, national, and international regulations, monitoring regulatory changes and assessing their impact
Requirements:
Proactive and able to manage multiple priorities effectively
Comfortable working in a fast-paced, regulated environment
Excellent IT skills, ability to use MS Office and pick up bespoke systems with ease