The latest Regulatory jobs - BETA

Excellent Regulatory Affairs Associate role working with a growing international pharmaceutical company.

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. ...

Come and join one of the world’s largest pharmaceutical companies and gain experience to further develop your career.

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

Gain an exciting and interesting role within regulatory affairs today, with a great company based south of London. Our client are looking for a Regulatory Project Manager/Consultant to come on board and manager their international projects across a range of different clients within the medical device industry. They are offering a job with great variety with a great salary package too.

Regulatory Affairs & Drug Safety Officer

My client is looking to hire a new Regulatory Affiars & Drug Safety Officer. You will be joining their expanding team in Leuven, a lovely little town sporting a medical university and a wide variety of European expats. The company itself is at the front of the field when it comes to stem cell research and cell regeneration.

A fantastic career developing role as a Regulatory Affairs Specialist has come with our client based in a great location in Germany. It is a great opportunity to develop your career and enrich your skills and expertise within regulatory affairs, in an innovative product range. If you are an experienced regulatory affairs professional, with expertise in the medical device industry...then we want to hear from you today!

The opportunity to join a leading and expanding pharmaceutical company who will provide stability and strong potential of career progression and more importantly great work environment.

Quality Assurance (QA) - QA and Regulatory Consultant A fantastic opportunity for a Quality Assurance (QA) and Regulatory Consultant to join a market leading multi national...

Job Title: Senior Regulatory Affairs Consultant Location: London Job Type: Permanent Salary: Up to £60,000 + additional benefits

Prestigious global pharmaceutical company requires a CMC professional with experience of working in NDA/MAA submission teams.

Prestigious global pharmaceutical company requires a number of CMC professionals to provide strategic and operational global CMC regulatory direction & documentation for projects/products covering development, registration and approval/post approval activities. All positions are permanent.

Roles available: Quality Engineer, Quality Assurance Specialist, QA/RA Manager, Quality Systems manager, Documentation Specialist, CAPA manager, Director Quality operations, Director Quality systems, Regulatory affairs Director, Technical file specialist, RA manager, Regulatory associate new product development

Director, Regulatory CMC!!
Top Specialist Pharma!! Superb opportunity for an experienced Regulatory Affairs CMC candidate with 8+ years. Based in Hertfordshire, this Director will be responsible for a Regulatory CMC Team and selected high-level Projects - Leadership, influencing, in-depth knowledge and expertise is required.

Medpace is a global, full-service clinical research organization with expertise and therapeutic specialization in cardiovascular, endocrine/metabolic, and oncology research. In a rapidly growing industry, Medpace has quickly become a global leader in providing pharmaceutical and biotechnology companies with customized solutions in the drug development process.

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

Regulatory Operations Associate - Permanent - Berkshire Shreeya Patel is working with a Global Management Consultancy to help recruit a Regulatory Operations Associate to join their...

Regulatory Operations and Publishing Manager - excellent package!!
Our client is a Top Company and seeks a Regulatory Publisher with approximately 5+ years experience. The candidate will have a broad-based knowledge of Regulatory Operations and Publishing across the EU and ideally, Globally.

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

Great Regulatory opportunity for a Senior Regulatory Associate/Officer with a background in Oncology and Post approval procedures. This top Pharma Co. is commercially very successful with a significant number of Products. A salary of up to £38,000 is offered plus excellent bonus and leading benefits. Hertfordshire location.

Great Regulatory opportunity for a European Regulatory CMC Associate/Officer with a background in Generics. This top Generics Co. is commercially very successful with a significant number of Products. A salary of up to £35,000 is offered plus leading benefits. Essex location.

A Freelance Regulatory Affairs Consultant is needed to join one of the world’s leading pharmaceutical clients based in the beautiful Buckinghamshire.

Come and join one of the world’s largest pharmaceutical companies and gain experience to further develop your career.

Are you looking for an interesting role within medical devices to work with a range of innovative products? Then this role as Regulatory Affairs Specialist could be what you are looking for. Our client are currently in the process of recruiting for a Regulatory Affairs Specialist to join their expanding and international team based in the UK.

A leading, global Pharmaceutical Company are looking to bring on board a Regulatory Affairs Consultant, for a 6-12 month contract, to their site just West of London.

Role:

- Regulatory lead for complex emerging market business integration projects.
- Prepare, manage and implement a plan to transfer marketing authorisation holder within emerging market regions. ...

A leading, global Pharmaceutical Company are looking to bring on board a Regulatory Affairs Consultant, to their site in County Durham.

Role:

- To provide Regulatory Conformance expertise to ensure products supplied by the site comply with the registered requirements of the receiving market, assuring the quality of these products at all times, enabling introduction of new products and release of established products to market. ...

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.