Job Description
The Regulatory Affairs Specialist will be responsible for supporting regulatory activities across various Abbott and Third Party Manufacturer sites.
Major Responsibilities
* Education: Bachelor's degree in a science field (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology).
* Experience: 2+ years in a GMP/Biotech/Pharma/Medical Device/IVD regulated industry, with a focus on Regulatory Affairs.
* Regulatory Knowledge: EU and international medical device regulations and submissions expertise.
Key Skills
* Matrixed team collaboration.
* Fast-paced environment adaptability.
* Documentation review and analysis.
* Quality documentation generation.
* Strong written and oral communication.
* Organisational skills and attention to detail.
About the Role
This position requires the ability to work independently and as part of a team in a dynamic business environment. The successful candidate will possess excellent interpersonal skills and be able to identify and resolve obstacles effectively.
What We Offer
A challenging role within a global organisation that values innovation and excellence. The opportunity to develop your skills and expertise in Regulatory Affairs and contribute to the success of our business.