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.
This role offers an exciting opportunity for a Regulatory Affairs Manager to oversee and deliver regulatory strategies within the Pharmaceutical industry.
The successful candidate will be responsible for managing regulatory activities and ensuring compliance with regulatory requirements.
Our client is a reputable player in the Pharmaceutical industry.
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.
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU 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.
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.