As the Regulatory Affairs Specialist you will be responsible for maintaining the integrity and compliance of medicinal product imports, ensuring the highest standards are met in line with industry regulations.
We are currently looking for a Regulatory Affairs Specialist to join a leading Distribution company based in the Kent area.
This will be a hybrid role consisting of 3 days on site and 2 days working from home.
Reporting to the Regulatory Affairs Manager, you will play a crucial role in ensuring regulatory compliance and supporting the successful submission of our products to global regulatory agencies.
We are seeking a talented Regulatory Affairs Specialist to join our client's regulatory team in support of the expansion of their ISO 13485 diagnostics product pipeline.
As Regulatory Affairs Specialist responsibilities include
Collaborate closely with the Regulatory Affairs Manager to develop and maintain technical files and submissions for global regulators.
In this role as a Regulatory Affairs Officer, you will be responsible for building regulatory strategy, determining applicable regulatory requirements, proposing solutions to comply with regulatory requirements, and managing product license registration with the appropriate regulatory authorities worldwide.
An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Department.
The Group consists of three divisions VetPlus - a global leader in companion animal nutraceuticals, Agri Lloyd, an agriculture focused unit and Mill Farm Sports Village a multi-purpose leisure complex incorporating a fully owned football club with associated facilities.
Tangerine is a successful, growing group of businesses based in the delightful seaside town of Lytham St Annes.
Regulatory Affairs Labelling Manager; Your new company
This consultancy is looking to strengthen their Regulatory Labelling group by taking on an experienced Regulatory Affairs Labelling professional for a contract job.
This job is outside IR35 and has scope for extension.
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.
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.
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.
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.