The latest Regulatory jobs - BETA

Working for a large and established medical device organisation you will be the Director of Regulatory Affairs spanning the Asia Pacific region.

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

This is an amazing opportunity to take your regulatory career to the next level! Would you like to work at the EU headquarters of one of the leading companies…do you like variation in your job, and would you like to work with different nationalities? If yes, this might be your opportunity! Please contact Marc Van de Voorde on +41-710.51.00 or alternatively send your CV to marc@advregulatory.com or cv@advregulatory.com

Our client, a world class pharmaceutical company driven by research and development, strives towards better health for individuals by developing safe, effective and innovative pharmaceutical products and now ranks as the fastest-growing among the UK''s top 50 pharmaceutical companies. They are seeking a Regulatory Affairs Manager for a 6 month contract at their South East UK location.

My client is one of the leading providers of Medical IVD products worldwide who have an outstanding reputation in the industry. A new requirement has arisen within their International regulatory teams for an experienced RA candidate to join as their newest Regulatory Specialist.

My client - based in Manchester - is looking for a Regulatory Specialist on a 3-6 month contract to deal with international registrations for medical devices.

On behalf of our Client we are looking to recruit a Regulatory Affairs & Pharmacovigilance Officer.

Senior Regulatory Officer required

Within this role you will provide strategic and operational regulatory direction for your respective region and support to the Global Program Regulatory Director for projects or brands and line extensions through development, registration, and approval/post-approval. The RPRM ensures the execution of regional regulatory plans in line with global regulatory strategy. ...

A global pharmaceutical based in Stockley Park are urgently seeking 3 Regulatory Affairs Consultants to come on board. For the right candidate they are willing to pay up to £40 an hour

Become a member of a small team providing support for the company’s CMC Research Dept in the development of products and supply of IMP. Office based in London with attendance at CMC Research & Production sites and at contractor/supplier sites throughout the world. This is a full-time, fixed-term (6 months) position which can either be a headcount position with basic pay plus benefits (pro rata) or freelance as a limited company on an attractive daily rate.

A chance to not only to work for a global leader in plasma protein biotherapeutics but also to join an expanding regulatory team in a permanent position with an attractive salary & benefits package and long-term career development opportunities.

Our client, a specialist global pharmaceutical company and innovative leader in pharmaceutical and health care research and development, is mainly concerned with development activities. They are seeking a Regulatory Affairs Manager for a 6 month contract at their Buckinghamshire site.

On behalf of our Client we are looking to recruit a Regulatory Affairs & Pharmacovigilance Officer. The successful candidate will report to the General Manager

An excellent opportunity has become available to work for a company that is currently looking to expand its Regulatory department. This company offers an excellent benefit package along with great career management strategies that ensure you are always satisfied with the direction your career is going.

Advanced Regulatory have a new contract role in the M4 corridor with rates up to £50 per hour. You will be working with a friendly team for a Global Blue-chip organisation. Ideally you will be able to start at the beginning of June and be happy in a role where you have full autonomy for your projects. Contact Theo Moore on 0207 801 3380 or email your Cv to CV@advregulatory.com highlighting your hourly rate and availability.

Work for one of the best companies in the UK.

Take this rare but great opportunity to work for a Top 20 Pharmaceutical company in a commercially focused role where you will interact extensively with cross-functional European and Global representatives including, medical, marketing, regulatory and legal – Contact Theo Moore on +44 207 801 3380 or email me your CV in confidence to Theo@advregulatory.com

Role: EU Regulatory Manager/Regulatory Affairs Location: Buckinghamshire Duration: 12 months Rate: Negotiable

ASSOCIATE DIRECTOR REGULATORY AFFAIRS, EASTERN EUROPE & RUSSIA FOCUS, LINE MANAGEMENT AND STRATEGY!! BERKSHIRE LOCATION!!

LINE MANAGEMENT AND PROJECT MANAGEMENT!!

Take the next step in your regulatory career and join a leading Pharmaceutical company in a strategic role where you will take the regulatory lead for a Centralised procedure planned for 2013. Contact Theo Moore on 0207 801 3380 or email me your CV to Theo@advregulatory.com

I am now recruiting for a Regulatory Specialist/Engineer to join a global leader in the orthopaedics market, on an 18month fixed term contract. My client specialises in design and manufacture of implants for replacement hips, knees, shoulders, bone cements etc and orthopaedic surgical instruments. Contact Boma on 0207 469 5255 or b.wokoma@progressiverecruitment.com

Regulatory Submissions Specialist, EC and RA submissions

Regulatory / Start-up / submissions / clinical trial specialist for Growing CRO in LYON. 1-3 years experience required. Fluent local languages and English ESSENTIAL

I am currently working alongside one of the world’s most well-known, well respected and most successful pharmaceutical companies, looking for a freelance regulatory professional with strong experience within the labeling arena to join their expert team in the UK. This is initially a 12 month contract, with strong potential to have this extended beyond that. My client is willing to be open to negotiation in regards to pay rates.

To apply for this regulatory affairs publisher role please call Julie Cooper on 020 8305 9733 or 07951 082482 Alternatively please send your CV to:

This global manufacturer of advanced cardiac rhythm management systems and vascular intervention devices requires an experienced Regulatory Affairs Manager who has previously worked in the medical drug/device arena.

Our client is a world leading independent biotechnology company aspiring to be the best human therapeutics company that discovers and develops important therapeutics, bringing meaningful improvement to the lives of people all over the world. They are seeking a Regulatory Affairs Manager for a 12 month contract at their Cambridgeshire or North West London location.

Regulatory & Scientific Affairs Manager Benelux – South of Brussels– Join a medium sized Biopharmaceutical Company with a great pipeline….!!! Please contact Marc Van de Voorde on +41-41-710.51.00 or alternatively send your CV to cv@advregulatory.com.

You will be acting as Global Program Regulatory Manager for a large global pharmaceutical company.

You are acting as Regulatory Affairs Manager for a global pharmaceutical company. Your main responsibilities include the preparation and submission of registration documents.

Regulatory CMC Manager - Switzerland - Zurich / Zug / Lucerne Region - Salary Negotiable. As the Regulatory CMC manager you will be responsible for preparing the Global Product Regulatory CMC submissions inclusive of IND's, NDA's and post approval stages.

Leading pharmaceutical company. Strategic regulatory support for new product initiative and for existing internal and external portfolio.

Associate Director, Regulatory Affairs required

Regulatory Affairs Publishing role - We are ideally seeking individuals from a strong and recent regulatory publishing background ideally having worked at a Pharmaceutical company in the past. The individual will be responsible for publishing submissions within the EAME region as well as Emerging markets. 100% office based in Buckinghamshire / Berkshire area.

A global pharmaceutical based in Stockley Park are urgently seeking 3 Regulatory Affairs Consultants to come on board. For the right candidate they are willing to pay up to £40 an hour

A global pharmaceutical based in Stockley Park are urgently seeking 3 Regulatory Affairs Consultants to come on board. For the right candidate they are willing to pay up to £40 an hour

Novella Clinical is a global, full service Clinical Research Organisation with our European Headquarters in Stevenage, Hertfordshire.

SENIOR/MANAGER REGULATORY AFFAIRS - REGULATORY STRATEGY, OTC/CONSUMER CARE, HIGHLY SUCCESSFUL COMPANY - BERKSHIRE!!

LEAD THE REGULATORY TEAM!!

As Regulatory Affairs Associate you will be assigned to each project team. Your main responsibility is to coordinate the regulatory and ethics submissions for the study. As Regulatory Affairs Associate you may be assigned to more than one project.

Regulatory Affairs Manager –office based, Maidenhead, UK As Regulatory Affairs Manager you will lead the coordination of our Global Regulatory Projects and gain the international clinical trials experience that you career deserves. This will include to coordinating and preparing submissions to various international authorities along with the ability to manage internal teams and handle regular contact with clients and agencies.

My client is a medium sized Pharmaceutical Consultancy, in the South East of England.

Leading pharmaceutical company. Strategic regulatory support for new product initiative and for existing internal and external portfolio.

Role: Regulatory Affairs Manager Location: London Duration: 6 months Rate: Negotiable

An exciting opportuniyt to join an international compnay and work on a Consumer Care Portfolio

Regulatory Affairs Manager, Emerging Markets Location: Middlesex A global pharmaceutical company based in Middlesex are currently recruiting for a Regulatory Affairs Manager within Emerging Markets. As Regulatory Affairs Manager, you will use your expertise in emerging markets to provide input into product strategy for the region, prepare International Market Applications for new products, reviewing post-marketing variations

Regulatory Affairs Supervisor - perm role - London Main duties and responsibilities: Preparation of licence applications and leaflet updates for both MHRA and EMEA Monitoring pending applications to...

Regulatory Affairs Manager - Development Team.

Permanent, full time, office based role for experience Regulatory Affairs Manager in pharma company.

For a confidential consultation call Beatriz de Luis on 0044 (0) 207 255 6665 or email your CV to beatriz.deluis@secpharma.com


Job Summary:

My client, growing global pharmaceutical company, is currently looking for an EU Senior Regulatory Affairs Manager to join its team in Madrid.

Senior Regulatory Affairs Associate

My client, a well known and reputable, biopharmaceutical company has an opening for an experienced Regulatory Affairs Associate or Senior Regulatory Affairs Associate to join there Regulatory department.

Regulatory Affairs Associate - 1 Year Fixed Term Contract

My client, one of the UKs leading pharmaceutical company, is looking for a Regulatory Affairs Associate to join the Regulatory Affairs department at the company''s Headquarters. This offers a great opportunity for someone to step into an established Pharmaceutical company and gain some exceptional experience.

A position has opened up with a global speciality pharmaceutical company with operations running in over 100 countries, that develops and commercializes innovative products covering a range of therapeutic areas. Contact Boma on 0207 469 5255 or b.wokoma@progressiverecruitment.com for more info.

I am currently recruiting for an Emerging Markets Regulatory Manager, to join a global pharmaceutical company with an extensive product portfolio and operations running in over 100 countries. This role is based in Buckinghamshire. Contact Boma asap for more information on 020 469 5255 or b.wokoma@progressiverecruitment.com

I am working with a global leader in the orthopaedics market. They are experts in the design and manufacture of implants for replacement hips, knees, shoulders, bone cements etc and orthopaedic surgical instruments. Contact Boma asap for more info on 0207 456 5255 or b.wokoma@progressiverecruitment.com

SENIOR REGULATORY AFFAIRS OFFICER, OR PROJECT MANAGER PHASES III AND IV AND POST MARKETING - BERKSHIRE!!

4+ YEARS REGULATORY AFFAIRS EXPERIENCE - WORK ACROSS THERAPEUTIC AREAS - EUROPEAN AND INTERNATIONAL SCOPE

REGULATORY OFFICER OR OFFICER, EUROPE FOCUS- LEADING EMPLOYER - ESSEX!!

EUROPEAN REGULATORY EXPERIENCE - NEW SUBMISSIONS, CMC/MODULE 3, MRP & DCP EXPERIENCE DESIRABLE!!

UK REGULATORY OFFICER - MIDDLESEX LOCATION!!

2-3 YEARS UK REGULATORY EXPERIENCE - VARIATIONS, MRP & DCP, LABELLING DESIRED!!

REGULATORY COMPLIANCE MANAGER, CMC/EU - CAMBRIDGE - LEADING UK SPECIALIST PHARMA!!

JOIN AN OUTSTANDING AND DYNAMIC REGULATORY AFFAIRS UNIT!!
4-5+ YEARS EUROPEAN REGULATORY AFFAIRS CMC EXPERIENCE REQUIRED

SENIOR/MANAGER REGULATORY AFFAIRS - REGULATORY STRATEGY, OTC/CONSUMER CARE, HIGHLY SUCCESSFUL COMPANY - BERKSHIRE!!

LEAD THE REGULATORY TEAM!!

My client are currently seeking a regulatory affairs manager, to build strength within an existing team.

My client are currently seeking a senior regulatory affairs officer, to build strength within an existing team.

Regulatory Affairs Project Manager / Leader - Global Development - Switzerland - Excellent Package

For a confidential discussion call Nikolay on +44(0) 207 255 6665 or e-mail nikolay.dimitrov@secpharma.com

Regulatory Affairs Manager - 6 MONTHS CONTRACT - Brussels

For a confidential discussion call Nikolay on +44(0)207 255 6665 or e-mail nikolay.dimitrov@secpharma.com

Sr Regulatory Associate / Junior Manager - Middlesex

Introduction

My client is a leading Fortune 500, Biotechnology Company. With headquarters in the USA, my client employs over 500 staff in their UK offices, located in Cambridge and Middlesex on both a permanent and contract basis.

A market leader, my client strives to develop products that change people''s lives and in the last 30 years have transformed the management of anaemia, inflammation,

Senior Regulatory Affairs Associate - Brussels, Belgium

For a confidential discussion call Nikolay on +44(0)2072556665 or e-mail nikolay.dimitrov@secpharma.com

Global Regulatory Manager - Development or Life Cycle Management - Switzerland

For a confidential discussion call Nikolay on +44(0) 207 255 6665 or e-mail nikolay.dimitrov@secpharma.com

Global Regulatory Affairs Manager - Switzerland - Permanent

My client, a large pharmaceutical company is looking for Global Regulatory Affairs Manager to join their team in one of their sites located in Switzerland. To find out more about the role and company please call Nikolay on +44 (0)20 7255 6665 / +41 (0)44 580 3717 or send your CV to Nikolay.dimitrov@secpharma.com

Global Regulatory CMC Manager - Switzerland

My client, an expanding mid-sized global pharmaceutical company, is looking for top Regulatory industry professionals to join their team. For more information call Nikolay on +44 (0) 207 255 6665 or send an e-mail to Nikolay.dimitrov@secpharma.com

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

To apply for this Head of Regulatory Affairs role please call Julie Cooper on 020 8305 9733 or 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk

Regulatory Affairs Manager Cosmetics please call Julie Cooper on 020 8305 9733 or 07951 082482 Alternatively 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

My client is large Pharmaceutical company in the South-East of England. You will be responsible for preparinmg and submitting high quality documentation for Regulatory Submissions.

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

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 manger 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 regulatry affairs manager 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 contact me at: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 contact me at: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 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 regulaotry affairs manager please call Julie Cooper on 0208 3059733 or 07951 082482 Alternatively please email me at: julie@mosaicrecruitment.co.uk

The Regulatory Information Manager will be responsible for ensuring Regulatory Operations helps deliver Takeda company goals, supports the Document Managent and Registration Tracking Systems.

You will have at least four years’ experience in a similar role, a medical/science background and excellent knowledge of the regulatory environment – including ICH, GCP and FDA. Team building, conflict resolution and negotiation skills are also essential

Regulatory Affairs Manager- Biotechnology. Singapore Please send your CV to Mark O'Halloran at Real Pharma m.ohalloran(a)real-pharma.com in order to be considered for this position.+65 6591 5600 Keywords: Regulatory Affairs Manager, Biotech, Biotechnology, NDA, ASEAN, Regulatory, Clinical trials, Post marketing, new drug applications.

Regional Regulatory Manager

My client, a world leading Pharmaceutical company, is looking for a Regional Regulatory Manager to provide strategic and operational regulatory direction for the region. The successful candidate will be part of a reputable company that leads the way in Pharmaceutical R&D and manufacturing.

SENIOR/MANAGER REGULATORY AFFAIRS - REGULATORY STRATEGY, OTC/CONSUMER CARE, HIGHLY SUCCESSFUL COMPANY - BERKSHIRE!!

LEAD THE REGULATORY TEAM!!

REGULATORY OFFICER OR OFFICER, EUROPE FOCUS- LEADING EMPLOYER - ESSEX!!

EUROPEAN REGULATORY EXPERIENCE - NEW SUBMISSIONS, CMC/MODULE 3, MRP & DCP EXPERIENCE DESIRABLE!!

SENIOR REGULATORY AFFAIRS OFFICER, OR PROJECT MANAGER PHASES III AND IV AND POST MARKETING - BERKSHIRE!!

4+ YEARS REGULATORY AFFAIRS EXPERIENCE - WORK ACROSS THERAPEUTIC AREAS - EUROPEAN AND INTERNATIONAL SCOPE

REGULATORY AFFAIRS MANAGER, PHASES I TO IV & POST MARKETING, BIOPHARMA - BASED IN CAMBRIDGE!!

LEADING INDUSTRY EMPLOYER IN THE UK!!

My client is looking for a EU Regulatory Affairs Executive to join their team.

REGULATORY AFFAIRS MANAGER, DEVELOPMENT - BUCKINGHAMSHIRE, SUPERB PACKAGE OFFERED!!

PROJECT MANAGEMENT IN DIFFERING PORTFOLIOS - REGULATORY DEVELOPMENT REGISTRATIONS & POST MARKETING FOCUS!!

SENIOR ASSOCIATE REGULATORY OPERATIONS AND PUBLISHING - EXCITING COMPANY - BASED IN BERKSHIRE!!

REGULATORY OPERATIONS AND PUBLISHING CONTRACT - TOP PHARMA - BASED IN HAMPSHIRE/SURREY!!

ISI TOOLS & PUBLISHING A STRONG PREFERENCE - eCTD''s /NeeS Experience!!

Study Start-up Leader with experience leading international Study start-up associates / specialists - TOP FIVE CRO. Only EU Citizens/permanent residents should apply

An impressive, top performing biotech company are looking to add to their headquarters in Switzerland. Join an exciting friendly organisation that has a keen interest in development. Known to interview and hire the best, joining this organisation will ensure a career path of value. You will have exposure to pioneering technology.

My client has a new role through company expansion for Regulatory Affairs Manager Project Manager, Under the responsibility of Team Leader of Regulatory Affairs and within the framework of dedicated projects, you will ensure international coordination of development projects to the regulatory portion (EU, United States, Japan and emerging countries).