The latest Regulatory Affairs / Reg affairs jobs - BETA

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.

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

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

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

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. ...

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 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.

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

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.

Pharmalink are currently recruiting for a Regulatory Affairs Associate-level candidate to work on a long term contract for an International Pharmaceutical organization. You would be joining our international network of consultants on a year’s contract. The ideal candidate would have about a year’s experience working in a busy regulatory environment and would have excellent organizational and communication skills.

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.

Senior Regulatory Affairs Officer - Global Pharmaceutical - MRP & DCP Experience - up to £35,000

Senior Regulatory Affairs Officer - Global Pharmaceutical - MRP & DCP Experience - up to £35,000

We are currently working with a top Global Pharmaceutical Company who is one of the leaders in their field. Due to company expansion they are currently looking for a senior Regulatory Affairs Officer to join their team close toManchester.

A young and developing medical device company based in Germany are currently in the process of recruiting for a Regulatory Affairs Specialist/Manager. This is a great opportunity to develop your regulatory affairs career in dynamic environment; allowing you to be part of the growth and success of their innovative product range. They are offering a competitive salary package and a permanent role.

Regulatory Affairs Specialist - Permanent - Berkshire Shreeya Patel is recruiting a Regulatory Affairs Specialist to join a global management consultancy at their site based in...

Our client is a specialist pharmaceutical organisation who have a great reputation in a number of different therapeutic areas. They are currently recruiting for a Senior Regulatory Affairs Officer based at the Leeds head office.

Reporting to the Principal Regulatory Officer key Responsibilities of this role include:

* Preparing product packaging and reviewing / submitting to external databases, liaison with user test team.
* Preparation of Type II MR variations. ...

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 busines

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

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 FDA experience? If so, do not hesitate and apply now!!

An excellent opportunity has arisen to join a leading Pharmaceutical company based in Hertfordshire as a Senior Regulatory Officer.

My client is a niche provider of innovative Medical Devices that are used throughout the world with ground-breaking results for thousands of patients. Due to the nature of their devices, it is increasingly important for my client to recruit the very best candidates within the industry and they are now looking to expand their Regulatory & Quality team with their newest addition.

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.

Regulatory Affairs Associate – Belgium - Antwerp - Brussels

Join this fast paced and dynamic top 5 global CRO for a permanent contract and gain great exposure to EU Regulations. ...

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

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

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

*New opportunity* for a Senior Regulatory Affairs Manager to join a global pharmaceutical company based in Buckinghamshire. A fantastic position with a specialist, high functioning team and a role that will offer great variety.

Regulatory Affairs Manager, Emerging Markets, Product Specialist is required to join a leading Global Biopharmaceutical company with a great reputation in the market place for their highly ethical and dynamic approach to business. Managing the Regulatory activities for one of my client’s therapeutic portfolios and exciting pipelines, you will have a developed understanding of country specific Regulatory requirements throughout the product life-cycle.

Are you looking for a new and exciting international role in a sunny location?

A truly international pharmaceutical company is looking for an experienced regulatory affairs manager to take over projects in regulatory affairs in their bio tech division.

The main purpose of this role is to obtain and maintain market authorisations as well as develop strategies for various market entries, especially in Latin America and in Asia. ...

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

Regulatory Affairs Manager in Zürich



Für ein führendes Pharmaunternehmen hier in der Schweiz suche ich aktuell nach einem erfahrenen Regulatory Affairs Manager mit einem Fokus auf Swissmedic Zulassungen.



Das Unternehmen bietet Ihnen eine vielseitige Position die, je nach Absprache, zwischen 60-100% sein kann.



Das Unternehmen ist ein weltweit führendes Unternehmen in der Pharma Industrie und der Medizintechnik. Mit weltweit rund 70. ...

This is a fantastic opportunity for you to join one of the world's leading medical device companies and further develop your career.

Regulatory Affairs Manager (m/f) Notre client en Suisse est actuellement à la recherche d'un Charge d’affaires reglementaires. Ce poste inclu toutes les activités visant à obtenir l'approbation réglementaire pour le développement, la fabrication, la commercialisation et la distribution de leurs produits.

Due to continued growth, PPD is recruiting for a newly created position of Regulatory Affairs Manager to support Ireland.

To apply for this regulatory affairs associate role please call Julie Cooper on 0208 3059733 or 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk

To apply for this senior regulatory affairs associate role please call Julie Cooper on 02083 05 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 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 020 8305 9733 or 07951 082482 Alternatively please send your 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 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 associate 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 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

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

My client, a global medical device company located in Galway is looking for a Regulatory Affairs Specialist to join a new and exciting regulatory affairs team.

Associate Director Regulatory Affairs - Central Melbourne Location - Senior Executive Position - Excellent Remuneration Package

This is a fantastic opportunity for you to join one of the world's leading medical device companies and further develop your career.

An urgent 12 month contract opportunity for a Senior Regulatory Affairs Manager (Biologics) has arisen with a leading Pharmaceutical company to work within their Amsterdam office.

Within this role you will provide and maintain regulatory support to obtain MAAs for commercial products and maintain these authorisations post-approval. ...

Full job description and company details are available upon application, apply below. This position is being dealt with by Rachael Matthews at Meet, call on + 44 203 178 7488 or +44 77 9441 1452 or via e-mail directly at Rachael@peoplewithchemistry.com to discuss in confidence.

We are currently recruiting for a Senior Regulatory Affairs Associate to join our Devices team - split between our offices in Park Royal, North London and Leamington Spa.

My Client, a leading biotech company is seeking a RA executive to join thier new product developement team for a 9 month contract.

Role responsibilities:
*Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval.
*Assists in developing procedures to ensure regulatory compliance. ...

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

This is a fantastic opportunity for you to join one of the world's leading medical device companies and further develop your career.

Regulatory Affairs & Quality Manager, Europe A global in vitro diagnostics company, based in Germany- Frankfurt, specialized in immunohematology and corresponding automation systems is currently looking for a Regulatory Affairs & Quality Manager, Europe

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. ...

An excellent career opportunity for a leading generic pharmaceutical company based globally as a regulatory affairs manager. This role offers excellent chances for career progression and provides a an excellent working environment with flexible working hours.

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

Regulatory Affairs Manager/Senior Regulatory Affairs Associate - Global Pharma - 5+ years experience - up to £60,000

Regulatory Affairs Manager/Senior Regulatory Affairs Associate - Global Pharma - 5+ years experience - up to £60,000

An exciting opportuniy has arisen for an enthusiastic and motivated individual to join the European Regulatory team, reporting to the Director of Regulatory Affairs responsible for the Pain therapeutic area.

Job title: Director, Global Regulatory Affairs Location: Mechelen, Belgium Salary: Negotiable dependent on experience

In the short-term you will be leading RA development, Scientific advice, agency interaction and regulatory strategy - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380

Join a first class organization that has both Pharma and Biotech products in development, Lead EU Strategy for Biotech submissions & Gain Global regulatory experience - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 -

The Salary for this role is up to £50,000 with a bonus and highly rated benefits package - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380

We have a new regulatory Affairs Executive role for a leading and innovative Pharmaceutical client based in Surrey. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore on +44 (0)207 801 3380

Join an organisation that has excellent training and development opportunities and interesting and commercially focused EU regulatory projects. The product range is varied and the scope for developing your experience and expertise is excellent. Please Contact Theo Moore on +44 (0)207 801 3384 or email your CV in confidence to CV@advregulatory.com

Join an organisation that has excellent training and development opportunities and interesting and commercially focused International projects. The product range is varied and the scope for developing your experience and expertise is excellent. Please Contact Theo Moore on +44 (0)207 801 3384 or email your CV in confidence to CV@advregualtgory.com

My client is a small succesful commercial biotechnology company based in Amsterdam. They have recently brought their first product to the International market and are continuing to expand the company R+D operations. They would like to add to the Regulatory Affairs team and hire a experienced Regulatory Affairs Manager with strong regulatory compliance and CMC experience.

To assist the Regulatory Affairs department in identifying key performance indicators & areas for improvement, and to ensure compliance with current regulatory policy they are now looking for a Senior Manager, Compliance & Training.

My Client, a leading CRO is looking for a regulatory affairs specialist to join their company in dublin for 6-8 month contract.

The Regulatory Affairs Specialist will provide regulatory advice and carry out projects in the provision of regulatory affairs services. ...

Regulatory Affairs Director, East Coast USA This is a truly exciting opportunity to join a currently expanding leading Global Pharmaceutical company as a Regulatory Affairs Director...

Regulatory Affairs Executive - 1 year/ 2 year Contract Role

A world leading pharmaceutical company based in the South East is currently looking for two regulatory executives.

Regulatory Affairs Manager - Technical role, prior management expereince is not essential, Sydney base, excellent remuneration package

Job Title: Regulatory Affairs Officer Location: Home Based anywhere Czech Republic Salary: Flexible dependent on experience

Job Title: Regulatory Affairs Associate Location: Home Based anywhere Czech Republic Salary: Flexible dependent on experience

Job Title: Regulatory Affairs Officer Location: Home Based anywhere in Poland Office Based in Krakow Salary: Flexible dependent on experience

An excellent opportunity has arisen to join one of the world's most prestigious pharmaceutical companies based in their Headquarters in Switzerland.

With an impressive product portfolio and strong pipeline, our client is looking for highly experienced Regulatory Managers to join the team.

Job Title: Regulatory Affairs Specialist Location: Home Based anywhere in Poland Office Based in Krakow Salary: Flexible dependent on experience

Regulatory Affairs Officer Location: Hertfordshire Employment term: Permanent An exciting opportunity within a global generics company, located in Hertfordshire, has arisen. They are currently recruiting for a Regulatory Affairs Officer on a permanent basis.

Regulatory Affairs Manager/Senior Specialist NPD (medical devices, Zurich)
Regulatory affairs, Project management; Switzerland; Manager; Luzern; Zug, Zurich,
Job Area: Regulatory affairs
Location: Switzerland (Zug area)
Industry: Medical device
Salary: £120,000-150,0000 package (Subject to relevant experience)
Contact: Elena.kyriacou@huntressgroup.com call: 0044 207 759 7790

My Client requires a RA specialist to join their team for a 9 month contract in Waterford.

The Regulatory Affairs Specialist is responsible for activities which lead to, and maintain regulatory approval to market devices. Additionally, the RA Specialist is responsible for assessment of device changes for regulatory implications.

Key Responsibilities:

-Working as part of a team responsible for Regulatory Activities and issues occurring. ...

Job Title: Regulatory Affairs Consultant Location: Berkshire/Buckinghamshire Salary: up to £50,000 Business Type: Specialist Regulatory Consultancy

Job Title: Senior Regulatory Affairs Executive Salary: Up to £60,000 Location: Oxfordshire Benefits: Additional benefits on offer

Job Title: Senior Regulatory Affairs Executive Salary: Up to €85,000 Location: Hamburg, Germany Benefits: Additional benefits on offer

My client, a leading, niche pharmaceutical company with a reputation for the development of innovative drugs to tackle the underlying causes of their area of specialism rather than just the symptoms, are currently searching for a Regulatory Affairs Officer to join their growing team in Brighton, UK.

A growing international Pharmaceutical Company is currently working exclusively with Real Pharma in the acquisition of a new Regulatory Branded Pharmaceutical team in Oncology and Pain. This multimillion pound organization has had exponential growth over the last 75 years and as a result is looking to fill these integral roles which will have massive impact to the success of the business.

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.

My Galway based client, is in need of a Regulatory Affairs Executive to Join their RA team for
an exciting 6 month contract. Working alongside the RA manager, this is an opportunitunity to broaden your hands on Regulatory experience in a start up Medical device company for a 6 month contract.

Role responsibilities:

•To assist the Regulatory Manager in preparing and reviewing submission packages to the IMB and MHRA in a timely manner. ...

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

Job Title: Senior Regulatory Affairs Executive Salary: Up to £50,000 Location: Middlesex/Berkshire/London Benefits: Additional benefits on offer

Job Title: Senior Regulatory Affairs Executive Salary: Up to £50,000 Location: Middlesex/Berkshire/London Benefits: Additional benefits on offer

Responsibilities will include; Review SPCs, artwork and PILs, prepare submissions including CMC variations, SPC, labelling and renewals and ensure documentation and submissions are on time and liaise with the authorities.

For further information about this role or to arrange a confidential conversation about other vacancies within regulatory affairs please contact Tim Barratt on +44 (0)1727 817 626 or send you CV to tbarratt@keypeople.co.uk

Our client is a highly reputable Regulatory Consultancy dedicated to providing services to the biotech and pharmaceutical industries who are looking for an experienced Regulatory Affairs Manager for their location in Essex. There is flexibility to take on a candidate at a more senior level depending on experience.

Regulatory Affairs Officer - Permanent - Hertfordshire Shreeya Patel is recruiting a Regulatory Affairs Officer to join an API manufacturer in Hertfordshire on a permanent basis. As...

Regulatory Affairs Officer Permanent Middlesex We have just started working with a new client, a smaller-sized pharmaceutical company based in Middlesex. 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.

*New Position available* for an experienced Regulatory Affairs Director – Emerging Markets .

This opportunity is for a leading Pharma company based just South of England not far from London. They are a large pharmaceutical organisation that is focused on discovering, developing and commercialising innovative pharmaceuticals, biologics, medical devices and over-the-counter consumer products. ...

Regulatory Affairs Manager – Belgium - Antwerp

Join this fast paced and dynamic top 5 global CRO for a permanent contract and gain great exposure to EU Regulations.

Job Title: Regulatory Affairs Manager / / Regulatory Affairs Executive
Location: Antwerp / Belgium / Antwerpen
Benefits: Competitive salary package

Job Responsibilities:
• Provide expert regulatory advice and ensure accurate compilation, management and tracking of submissions. ...

Senior Regulatory Affairs Specialist - Medical Devices

Senior Regulatory Affairs Manager 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 to provide support on global regulatory projects.

On behalf of our client, we are currently recruiting for a Regulatory Affairs Advisor for Muster. This role will be mainly based in South Tipperary/Waterford. Flexibility in terms of location would be an advantage.

My client, based in Cork, is seeking an RA officer with 2 years of experience, in a regulated environment, preferably medical devices. This position is a fantastic opportunity to gain great experience for an exciting 6 month contract. ...

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

For this role you will be joining a team, within UK/Ireland and the EU.

Role:

- Accountable for ensuring EU contribution to Global Regulatory Strategies and that implementation plans are developed.
- Ensures regulatory plans are monitored, progress/variance communicated to Senior Management. ...

As we further build capability across the MEA Region, Hospira has identified an opportunity for an experienced Regulatory Affairs Associate to join our Regulatory Affairs Team in Dubai. Excellent salary and benefits package on offer including healthcare and housing

Regulatory Affairs Manager – CMC 12 month FTC (with likelihood of going permanent) Surrey £competitive salary. Due to expansion in the current team, a Regulatory Affairs Manager CMC position has arisen within the Animal Health department of one of the most sought-after and reputable pharmaceutical companies.

Regulatory Affairs & Quality Manager Standort: Oesterreich Sicherstellung der Kommunikation innerhalb des Konzerns und entsprechend der nationalen und europäischen Vorgaben Leitung des lokalen Qualitäts- und Beschwerdemanagements Implementierung und Optimierung regulatorischer und qualitätsrelevanter Maßnahmen und Prozesse

My client is looking for a Regulatory Affairs person, the title of the role will be down to the candidates experience, must have at least 1 and a half years previous experience within Regulatory Affairs.