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.
As the Regulatory Affairs Manager you will be responsible for EU regulatory activities including lifecycle management, submissions to EU regulatory bodies, preparing for new MAAs and developing regulatory strategy (throughout product lifecycle).
Walker Cole International is searching for a Regulatory Affairs Manager to join a global pharmaceutical company.
The main responsibilities of the Regulatory Affairs Manager will include
Module 1 compilation, artwork management & approvals, submission of new Marketing Authorizations.
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.
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.
As a Senior Regulatory Affairs Manager, you will be a vital member of our regulatory affairs function, responsible for setting the strategic direction and, working with expert third party advisors, ensuring compliance with all relevant regulations and guidelines governing our products and operations.
Well known and respected Wellness brand are looking for a Senior Regulatory Affairs Manager who has experience in Herbal Medicines (ideally) Medical Devices and Cosmetics
Reporting directly to the Group Head of Product Integrity, you will play a crucial role in developing and executing regulatory strategies, leading regulatory submissions, and managing a team of Regulatory Affairs Associates.
As a Senior Regulatory Affairs Manager, you will be a vital member of our regulatory affairs function, responsible for setting the strategic direction and, working with expert third party advisors, ensuring compliance with all relevant regulations and guidelines governing our products and operations.
Well known and respected Wellness brand are looking for a Senior Regulatory Affairs Manager who has experience in Herbal Medicines (ideally) Medical Devices and Cosmetics
Reporting directly to the Group Head of Product Integrity, you will play a crucial role in developing and executing regulatory strategies, leading regulatory submissions, and managing a team of Regulatory Affairs Associates.
We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products.
The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe.
You will grow and maintain major portfolio in particular for the European region, you will coordinate changes to existing products/dossiers keeping them on the market.