This position offers an excellent opportunity to gain valuable experience in the field of Regulatory Affairs (RA). Whether you are a recent graduate, career mover or have some experience within RA already, we want to hear from you!
About the Role
Our RA Coordinator works closely with the QARA team and wider departments to ensure Perspectum adheres to applicable regulations and standards, facilitate the preparation of regulatory submissions, and maintain accurate regulatory documentation.
Duties include:
- Preparing and submitting regulatory filings, reports and registrations
- Ensuring alignment between regulatory compliance and quality management systems
- Regulatory research for new target jurisdictions
- Representing the department at internal and external audits
For full details about the role and what we are looking for, please download the full job specification under ‘Information’ on the right hand side of this screen.
About You
To be considered for this role, you will have a Life Science or Regulatory based degree (or equivalent experience) to provide a good foundation of knowledge in which to build upon. Any experience working in a regulated environment, especially the medical device industry, would be highly beneficial but is not essential.
Most importantly, we are looking for an individual with a strong willingness to learn, excellent communication skills and a collaborative and proactive mindset.
About Us
All our benefits information can be found in the downloadable Benefits document under 'Information' on the right hand side of this screen.
At Perspectum, we are committed to fostering diversity, equity, and inclusion. We prioritise hiring based on merit, skills, and qualifications, valuing individuals for their unique contributions while ensuring a culture that respects and celebrates differences. If you require any reasonable adjustments as part of your application process, please let our Talent Team know.
