They are searching for a regulatory affairs professional to join them in tackling important sector challenges, ensuring they stay ahead of industry risks.
This individual will be critical in contributing to major sector reforms and conversations, from product health and safety to the organisation's contribution to climate change.
A great opportunity to work with a leading and trusted organisation.
Key responsibilities for the Regulatory Affairs Officer
Ensure Regulatory compliance with drugs imported overseas.
Lead any changes within the regulations and ensure the QMS is complaint with these.
General
I am currently working with a Parrell Import organisation based in North East London, this is a great opportunity for someone wanting to progress their career and join a friendly team.
The role has become available due to the forthcoming retirement of the current Head of Regulatory Affairs.
The Lloyd's Market Association (LMA) has a vacancy within its Legal and Regulatory team, reporting to the Head of Regulatory Affairs, which will encompass all aspects of regulatory and compliance support to the market, including managing several committees alongside the rest of the legal and regulatory team.
An excellent role on offer for an individual with strong regulatory affairs experience within the medical device sector looking to play a key role at an industry leading company.
Do you have regulatory affairs experience within the medical devices sector?
Would you like to work for a world leading company?
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved.
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract.
Other responsibilities include
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.