The latest Regulatory jobs - BETA

To apply for this regulatory affairs manager role please call Julie Cooper on 020 8305 9733 or 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk

To apply for this regulatory affairs manager role please call Julie Cooper on 020 8305 9733 or 07951 082482 Alternatively please send CV to: Julie@mosaicrecruitment.co.uk

To apply for this regulatory affairs associate please call Julie Cooper on 0208 305 9733 or 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk

To apply for this regulatory affairs role please call Julie Cooper on 0208 305 9733 or 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk

To apply for this regulatory affairs role please call Julie Cooper on 0208 305 9733 or 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk

To apply for this regulatory affairs medical devices role please call Julie Cooper on 0208 305 9733 or 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk

Are you looking for a new challenge? Do you possess FDA experience? If so, do not hesitate and apply now!!

Regulatory Affairs Consultant needed to join one of our pharmaceutical clients based in the beautiful Buckinghamshire.

Regulatory Product Specialist – Emerging markets

A truly exciting opportunity has come up to work for one of the most cutting edge, dynamic and high achieving companies in the market. The role is aligned to a specific therapy area and will require someone to perform the Clinical Trial Submissions for the product. ...

Regulatory Affairs Associate - UK

An exciting opportunity has become available for an exciting, dynamic and high achieving Biotech company. You will be part of the Rest of World Regulatory team and have strong local knowledge of Emerging Markets. ...

Within a team of regulatory professionals in Pharma Regulatory Affairs, based either at headquarters in Basel, Switzerland or our Development site in Welwyn, UK, several roles are being opened. You will be in a leading role in Pharma Regulatory Affairs

Regulatory Affairs Contractor - 6 Months - Operations

This is the opportunity for someone to join the Regulatory Affairs team with my client for a 6 month contract. The aim of this role is to help aleviate the work load of the team via operations such as the preparation of submission documents and the tracking of regulatory forms.

Areas of responsibility:



* European and swiss medic Submission Publishing of all submissions from a european perspective and dispatches to european and swiss Health Authorities (Swiss medic, EMA).



* Accountable for all Publishing, verification, dispatch and management of submission dossiers for all (investigational, marketing authorization, lifecycle management, post approval change management), e-CTD, NEES, Paper.

It’s the variety of the pipeline here that really makes the difference and you will be well matched with a product that suits your expertise - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100

Receive an excellent salary of up to 95,000 Euros plus a fully expensed car and bonus up to 15% - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100

Our client is a Global leader and pioneer in the Biotechnology field using innovative research to drive the discovery and development of important therapeutics. This top company has a strong development pipeline with strong prospects in Oncology, Osteoporosis and Renal. They are currently seeking a Senior Associate Regulatory Operations for a 12 month contract based in Cambridgeshire.

This is your chance to work with a global Pharmaceutical company, recognised as the major brand in countries worldwide. The company continuously grows in size and success, and is offering a great opportunity for a Regulatory Affairs Manager The role itself will provide you with excellent responsibility and broad accountabilities and is an ideal role for an experienced Regulatory Professional. With a focus on their employees, the company will ensure stability and growth in your career.

Associate Director - Regulatory Affairs, Emerging Markets

An exciting opportunity has come about to join a fast paced, dynamic company biotech that is leading the way in new medicines. My client is looking for an Associate Director of CMC to join them to help develop strategy for the Emerging Market regions. ...

An exciting and challenging opportunity has arisen to join the International Regulatory Affairs group based in the UK. My client is looking for a Senior Regulatory Associate, to join their expanding team.
The position is in the Emerging market team where you will be providing regulatory support to activities in markets outside of the EU/US and be directly involved in writing and preparing regulatory documentation. ...

My client is looking for a Senior Regulatory Affairs Consultant to join their growing team. You must have a good amount of previous experience in Regulatory Affairs and CMC/Quality and/or non clinical and clinical aspects.

Regulatory Affairs CMC Director, working for a leading global pharmaceutical company

Regulatory Affairs Line Manager, HOME BASED Career

£40.000 - £60.000

Are you interested in working from home? My client is looking for Regulatory Affairs Line Managers who are looking for career progression while working from home. This home based position offers you more flexibility in your work hours, and therefore a more balanced home life. Furthermore, working from home will safe you the stress of a daily commute.

This is a great opportunity to lead international projects in a management role within regulatory affairs. This is an interesting, permanent role to work as Regulatory Consultant, in a project management role. You will be working a range of innovative medical devices and combination products. Our client are offering a competitive salary package too.

Regulatory Affairs Associate required for permanent role with Novella Clinical. Office based in Stevenage, Herts.

Senior Regulatory Affairs Associate - Lifecycle Management Business type: Large Pharmaceutical Company Location: Buckinghamshire, Berkshire, England, UK Salary: Up to £43,000 + Bonus + Benefits

My client is one of the leading Service providers for the Pharmaceutical and Biotech industry with their brand being recognised for excellence. One of the key areas of their business is their Regulatory Consultancies which they are looking to expand by acquiring their newest Senior Consultant.

I am currently looking for a high-performance Senior Medical Writer to join our client's dynamic international medical and scientific writing team on a full-time basis.

Are you looking for a part-time opportunity in a leading medical device company, that will provide you with flexibility? Then this role as Regulatory Affairs Manager could be the ideal role for you. Our client are looking to take on someone to work 50% of the time, in a project management role for the emerging markets. It is an interesting role, which will provide the ideal setting for those looking for flexible working hours.

Regulatory Affairs Associate required for permanent role with Novella Clinical. Office based in Stevenage, Herts.

Senior Regulatory Professional - 5 month contract - South East Shreeya Patel is recruiting a Senior Regulatory Professional to join a global pharmaceutical company at their...

Senior Regulatory Affairs Officer - Permanent - West Yorkshire Shreeya Patel is recruiting a Senior Regulatory Affairs Officer to join a UK based Pharmaceutical company based...

Prestigious global pharmaceutical company requires a CMC professional to drive global regulatory strategy for medical devices & combination products throughout the product lifecycle, with a focus on creativity and innovation.

As a highly regarded Regulatory CMC professional, you will be an integral member of a small team providing high quality strategic regulatory and operational support & advice for the pharmaceutical development, maintenance and lifecycle management of research compounds and marketed products to ensure timely authorisations in line with clinical and commercial business needs.

This opportunity is your chance to make a significant contribution to an expanding, already successful company. This is a highly visible senior leadership role encompassing a variety of responsibilities and will require a well experienced industry professional with strong functional expertise as well as an outgoing, bubbly personality with the drive and determination to grow alongside the business.

This opportunity is your chance to make a significant contribution to an expanding, already successful company. This is a highly visible senior leadership role encompassing a variety of responsibilities and will require a well experienced industry professional with strong functional expertise as well as an outgoing, bubbly personality with the drive and determination to grow alongside the business.

Job Title: Regulatory Medical Writer Location: West Sussex, England, UK Salary: up to £32,000 + addition

If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100

Are you looking for a new challenge? Do you have international experience? If so, do not hesitate and apply now!!

Senior/Regulatory Officer - Top 10 Pharma, Buckinghamshire location!!
Great Regulatory opportunity for a Regulatory Associate/Officer with a background in International & Emerging Markets. 2 to 4 years Regulatory experience required. A competitive salary is offered plus leading benefits.

Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for providing delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and review and finalization of essential documents required for site initiation.

Senior Manager Regulatory Affairs, Medical Devices for a top Specialist Pharma Company!! This company rarely recruits in Medical Devices and is a top employer in the UK. 6+ years Regulatory experience is required; Project management and supervision of a small team. Buckinghamshire location. Good salary package!!

Regulatory and Pharmacovigilance Specialist/Manager - Central Switzerland - Pharmaceutical

Senior Manager Regulatory Affairs, Medical Devices for a top Specialist Pharma Company!! This company rarely recruits in Medical Devices and is a top employer in the UK. 6+ years Regulatory experience is required; Project management and supervision of a small team. Buckinghamshire location. Good salary package!!

The Local Regulatory Affairs Associate is responsible for preparing, submitting and following up on initial and amended Ministry of Health (MoH), Central Independent Ethics Committee (IEC), and any other central submissions required in the country(s) they are responsible for, within contracted timelines and budget, in accordance with local regulatory requirements and sound scientific/technical principles, including the creation and modification of documentation required for approval.

My Client, a global leading Medical Device company are looking for a Regulatory affairs Specialist to join there expanding RA team in their Galway facility for a 6-8 month contract.

Responsibilities: ?Determines global regulatory pathways for various projects including product classification and type of regulatory submission or rationale required.
?Participates on various teams to define regulatory requirements for EU, U.S. and international submissions. ...

A leading global Pharmaceutical company are looking to bring in a CMC Regulatory Affairs Senior Manager to be based in Netherlands.

A leading global Pharmaceutical company are looking to bring in a CMC Regulatory Affairs Manager to be based in Netherlands.

Regulatory Affairs Consultant
12 month contract

To apply for this regulatory affairs medical devices role please call Julie Cooper on 0208 305 9733 or 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk