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.
They are searching for a regulatory affairs professional to join them in tackling important sector challenges, ensuring they stay ahead of industry risks.
A great opportunity to work with a leading and trusted organisation.
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.
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.
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.
As Regulatory Affairs Specialist responsibilities include
Collaborate closely with the Regulatory Affairs Manager to develop and maintain technical files and submissions for global regulators.
We are looking for a regulatory affairs professional to join a chemical products manufacturing business.
Key elements of the role include regulatory research and analysis, maintenance of key chemical regulatory documents, compilation of regulatory dossiers to support product approval globally and, authoring and maintenance of safety data sheets.
This is a challenging and diverse role within a friendly regulatory team that offers excellent career development.
An opportunity has now become available for an experienced Regulatory Affairs Manager to join the company and undertake a leading role in product compliance with industry standards and regulatory requirements.
As a fully regulatory compliance facility, our client are able to provide technical innovation supporting with the formulation and development of novel cleaning products across many sectors.
Our client is an established contract manufacturing organisation (CMO) providing services on a global scale.
The successful Regulatory Affairs Specialist / RA Specialist will have hands-on knowledge of FDA regulations, ISO standards & SaMD - as well as proven experience working with medical devices that use AI & Machine Learning.
Regulatory Affairs Specialist, RA Specialist, FDA, 510(K), SaMD, Remote, COR5716
This is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field.
Your duties as the Head of Regulatory Affairs and Pharmacovigilance will be varied however the key duties and responsibilities are as follows:.
General
As the Head of Regulatory Affairs and Pharmacovigilance you will be responsible for providing organisation with strategic advice for the launch of new products in EU & UK..
We are currently looking for a Head of Regulatory Affairs and Pharmacovigilance to join a leading Pharmaceutical company based in the Kent area.
This role is responsible for the delivery of the company's development regulatory roadmap.
About the Company
We deliver innovative, cost effective and quality products and solutions for the advanced wound care industry helping to improve patient care and wellbeing.
We are an innovative medical devices manufacturer of advanced wound care products, including combination products, from gelling fibres and fabrics.