The latest Regulatory jobs - BETA

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 manager / associate role please call Julie Cooper on 0208305 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 020 8305 9733 or 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk

To apply for this regulatory affairs devices 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

Regulatory Affairs Specialist - Global Projects

Are you ready to manage your own projects? Then this could be the role for you! My client is looking to bring on a new consultant to join their highly successful team. Each consultant works on their own projects meaning you gain extensive experience in Regulatory Affairs on a global scale! In turn giving your CV an attractive boost and making you more employable in the future.

Have you got expertise within ISO 62304 and dealing with software life cycle? Then we want to hear from you today and inform you of a unique and interesting Regulatory Affairs Manager role based in Germany. This is a great management role within regulatory affairs for a developing start-up company. You will gain international experience and get to be part of this company's growth and excellent future prospects.

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 Regulatory Affairs Associate, CMC for a 12 month contract based either in South East UK or East Anglia.

Position provides customer-focused leadership in the execution of the start up of sites in one or multiple Phase II through Phase IV clinical trials across all functional Site Start-Up (SSU) areas.

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

A world class global CRO is seeking a Senior Director of Regulatory Affairs. You will be responsible for Matrix managing staff globally. Full life cycle development, business development as well as growing and managing client base and direct reports. For more information call me on +44 (0)1293 776644 or email gavin@barringtonjames.com

Our client is a world leading company aspiring to be the best in the discovery and development of important therapeutics. They are currently seeking an experienced Senior Regulatory Affairs Manager to join the Global Regulatory Team for a 12 month contract. This role can be based either in the South East or the East of England.

Our client is a world leading company aspiring to be the best in the discovery and development of important therapeutics. They are currently seeking a Regulatory Affairs Manager, Emerging Markets for a 6 month contract. This role can be based in either of their sites in North West London or East of England.

Superb role for a Regulatory Affairs Manager/Senior Manager with a background in Biotech or Vaccines. High-level Project Management and line management responsibility. Regulatory Development and Life-cycle management across the EU. High-tempo role for ambitious Manager wanting to progress your career. Superb Italian location.

Superb role for a Regulatory Affairs Manager/Senior Manager with a background in Biotech or Vaccines. High-level Project Management and line management responsibility. Regulatory Development and Life-cycle management across the EU. High-tempo role for ambitious Manager wanting to progress your career. Superb Italian location.

To apply for this regulatory affairs 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 / associate role please call Julie Cooper on 0208305 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 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 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

Regulatory Affairs Consultant - Project Management

My client, a high end consultancy, is looking to bring a new Regulatory Affairs professional into their dynamic team. Working for this consultancy will give you the experience of managing your own projects, including dealing directly with the client giving you a varied job role.

Head of Regulatory Affairs - Strategic Role - Prague

My client is looking for a strategically orientated individual to take on the position of Head of Regulatory Affairs in Prague. This opportunity gives you the chance to live in one of the most beautiful cities in Europe along with the chance to visit clients throughout the EU.

Regulatory Affairs Officer - Generics We have just started working with a new client, a smaller-sized generics company based in Central London. This is a permanent role and would offer a candidate who is already working in regulatory affairs in the UK, the chance to take the next step in his/her career and join a company that are poised on the brink of expansion.

Regulatory Affairs Manager\Senior Manager Emerging Markets. Permanent. Cambridge or Uxbridge We have just started working with one of the most reputable biotech pharmaceutical companies in the UK and they are now seeking a Regulatory Manager and Senior Manager to join their Emerging Markets team. These are both permanent positions based either in Cambridge or Uxbridge. Unfortunately there would be no scope for home working with these roles.

Are you looking for an exciting new challenge within Regulatory Affairs?
Are you ready for an interview in June 2013?
This an opportunity to join a highly skilled and motivated team within a Top name in the pharmaceutical industry.

A large global pharmaceutical company, with a broad portfolio of products currently has an opening within their large UK site for a Regulatory Programme Manager within their established Regulatory Affairs department located in the South East. ...

Contract opportunity available for a Regulatory Affairs consultant with a strong labelling background.

Job Title: Head of European Regulatory Affairs Location: Brussels, Belgium Business Type: Small, specialist Pharmaceutical Company Salary: Up to €160,000

The Regulatory Affairs Specialist provides project representation and input to projects awarded to my client for all stages of the drug development cycle.

A new opportunity has become available with a niche pharmaceutical company based in Central London as (Senior) Regulatory Executive. The role would be responsible for Registration and Post Approval activities of the company's new and existing products in the EU region. Applicants must have strong experience with CMC, MAAs, Variations, Renewals, Labelling, MRP/DCP/National procedures. Excellent opportunity for and experienced Regulatory Officer/Associate (2-4 years) to prog

Regulatory Officer - Central London location!!
Great Regulatory opportunity for a European Regulatory CMC Associate/Officer with a background in Generics. 2 to 4 years Regulatory CMC experience required. This top Generics Co. is commercially very successful with a significant number of Products. A competitive salary is offered plus leading benefits. Central London location.

Regulatory Officer - Central London location!!
Great Regulatory opportunity for a European Regulatory CMC Associate/Officer with a background in Generics. 2 to 4 years Regulatory CMC experience required. This top Generics Co. is commercially very successful with a significant number of Products. A competitive salary is offered plus leading benefits. Central London 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.

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.

Have you got expertise at management level within regulatory affairs, dealing with the APAC region? If so, then this could be a great opportunity for you to be the key expert for our client's medical device registration process within the APAC and African markets. You will gain great management experience and get to work a range of interesting projects. You will be offered a competitive salary, with a secure permanent role.

A permanent role is available for a Senior Regulatory Affairs Manager in a reputable mid sized pharmaceutical company for either the Cambridgshire, UK location or in Limburg, Germany. My client specializes in a niche product market and is looking for a Regulatory Affairs professional with an in-depth knowledge of current legislation and relevant Regulatory Guidelines to help impact their business and lead an expanding team.

Senior Regulatory Affairs Specialist - Medical Diagnostics

A fantastic Regulatory Affairs Specialist role has come up with our client based in the German speaking part of Switzerland, within the canton of Zurich. It will be your role within this opportunity to work on exciting international projects across a range of innovative devices. As this is a fairly young company, you will get to be directly part of driving their future success.

My client is a large Biotech company that works with a number of products within a number of countries; you will be working within the Global Regulatory Team in either the EU/Swiss department or within the Emerging Markets

Head of Regulatory Affairs required to join a global pharmaceutical company in Southern Germany on a permanent basis to manage the Strategic Partnership with an international CRO for Regulatory Affairs . This is a fantastic opportunity to secure a senior position within a well established international company.

Regulatory Affairs Director with experience in Immunology, Rheumatology or Neurodegenerative disorders required to join a market leading Pharmaceutical company in Southern Germany on a permanent basis. This is an excellent opportunity to join a growing team within a well established global company.

Would you like the option to work a permanent or 12 month fixed term contract for a stable pharmaceutical company in either the Cambridgeshire area or in Germany? Are you looking for a management role in Regulatory Affairs with career growth potential in a rapidly expanding niche product company? Than this may be the right role for you!

Regulatory Affairs Consultant - Top Consultancy

My client, a high end regulatory affairs consultancy, is looking to add a new consultant to it's team. The very nature of a consultants work is varied and flexible meaning you will receive incredible job satisfaction thanks to the possibility of working on multiple projects and case studies.

Regulatory Submissions Manager / Study Start-up Project Manager – SCOTLAND part home based Please contact Zoe Benningfield on 07896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

A global pharmaceutical company are looking to bring in a Regulatory and Development Manager to work on Animal Health products, based in Berkshire

Job Title: Regulatory Affairs Operations Assistant / Reg Ops Assistant / Regulatory Publishing Assistant / Regulatory Affairs Publisher

Location: Commutable from Cambridgeshire / Hertfordshire / Essex / East Anglia

Benefits: Generous hourly rate and solid training

Excellent opportunity for a Regulatory Manager to progress their career in a world leading pharmaceutical company. This newly created position would be responsible through the full regulatory cycle, form development to registrations and post approval activities. Highly desirable company and location. Excellent salary and benefits.

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

Gain management expertise and be part of company wide decisions, with this great Regulatory Affairs Manager role. Our client are a start-up company based in the North of Germany. They specialize within innovative and new technology medical devices. Not only is this a great role to develop your management expertise, you will gain an interesting and varied working life. They are also offering a competitive salary package.

Role: Regulatory CTA Consultant
Duration: 6 months
Location: High Wycombe
Rate: £30 - £35P/H

This position is responsible for managing / assisting in all regulatory aspects for Phase 1 - Phase 4 clinical trial authorization applications conducted globally, regionally or locally, spanning all therapeutic Areas.

Prestigious global pharmaceutical company requires a number of CMC professionals to drive global regulatory strategy for development projects and/or marketed products throughout the product lifecycle, with a focus on creativity and innovation. All positions are permanent.