The latest Regulatory Affairs / Reg affairs jobs - BETA

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.

Regulatory Affairs Associate - Cambridgeshire - Contract Shreeya Patel is recruiting a Regulatory Affairs Associate to join a global biotechnology company at their site based in...

Job Title: Global Regulatory Affairs Director Location: Munich, Germany Salary: Up to €95,000 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

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 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 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 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 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

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

Regulatory Affairs Consultant - Global - Travel

Looking to expand your experience? Want to work on a world wide scale? This could be the opportunity for you! My client is looking to add a new member to their already successful team. With clients ranging from a few miles up the road all the way to New Zealand this role really does encompass the world. Due to managing your own projects, should the need arise you will be able to visit clients no matter the destination.

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

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

Job Description:



A Global Pharmaceutical company based inCaliforniais looking for a Senior Regulatory Affairs Associate to add to their expanding team.

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.

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

Global Snr Regulatory Affairs Manager - Central London

My client is looking for someone to join their worldwide corporation in London. This is a chance to work on their Immunology and Respiratory drug portfolio which in turn will provide you with excellent variation in your average working day. Thanks to an ever increasing pipeline this variation will remain for years to come.

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. ...

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

Interim Associate Director of Regulatory Affairs for Europe working to implement regulatory strategy for selected drug development candidates and/or marketed products.

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.

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.

Reg Affairs Consultant - High End Consultancy

My client, a high end consultancy, is looking for an experienced Regulatory Affairs consultant to join their team. This is the chance for you to broaden your knowledge in Regulatory Affairs around the world working on important contracts.

Would you like to work for a reputable pharmaceutical company known for its niche product market? Are you looking contract position with a company that will give you career growth opportunities? My client is looking for an experienced Senior Regulatory Affairs Associate to join their expanding team for a 12 month contract in either the Cambridgeshire, UK or Limburg, Germany locations.

Senior Regulatory Affairs Specialist - Medical Devices

Senior Regulatory Affairs Manager, Marketed Products in Internal Medicine – Germany – 80,000 Euro to 90,000 Euro + bonus

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.

Looking for a new exciting opportunity? My client, a market leading medical device company is looking for a Regulatory Affairs Specialist to join there RA team for a 6 Month contract.

As a Regulatory Affairs specialist you will be responsible for activities which lead to, and maintain regulatory approval to market devices. Furthermore, to carry out assessment of device changes for regulatory implications. ...

Regulatory Affairs Consultant - Development

My client are offering the chance for a Regulatory Affairs professional to join their consultancy. With business profitable and plenty of work on hand they have decided to bring someone into the fold and help broaden their regulatory affairs knowledge.

Are you a regulatory affairs professional? Come from a CRO background? Looking for an exciting new role? The I have the perfect opportunity for you as my client, a global CRO is recruiting for a Senior Regulatory Affairs Specialist to be home based in Poland. My client is willing to pay a very competitive salary package plus benefits with a great career prospect.

Accenture is looking for Regulatory Affairs and Operations Specialists

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

inVentiv Health Clinical (formerly known as Pharmanet i3) are currently seeking a Senior Regulatory Affairs Associate for a freelance contract within our CRO operations. The contract would be full time for 8 months.

I am currently working with a Global Pharma to develop a new Oncology and Pain Regulatory team. This Global branded Pharmaceutical Company has recently been through an acquisition in Europe. As a result they are building a new team in their EU Headquarters which is based in the UK.

Therefore I am looking for 5 individuals who are keen to be involved in these exciting and rare opportunities. Please find some brief details below.

Snr Regulatory Affairs Manager - Top 15 Pharma

Looking for the next step up in your career? Want to work for a multi-national organisation? This could be the opportunity for you. My client is a top 15 Pharma who are looking for someone to step up into a Senior Management position. Notorious for providing excellent support and training for their employees, this is an excellent chance to move up the career ladder.

A Leading Biotech Company are presently looking to bring in an Interim Regulatory Affairs Director to lead and manage a large team of Regulatory Professionals. The role will be based in Berkshire.

Leads the Emerging Markets (EM) Regulatory Affairs team, including in-country Regulatory Affairs.

Is accountable for the definition of regulatory strategy and subsequent implementation, to ensure the successful registration of pharmaceutical products in EM. ...

A Global Pharma company are presently looking to bring in a Senior / Regulatory Affairs Consultant to their CMC group, within the EU team to be based in the Hertfordshire office, on a contract basis.

Role:

- Preparation of high quality, chemistry manufacturing and control (CMC) detailed regulatory documents using varied information sources.
- Liaising closely with other personnel to ensure accuracy of such documents. ...

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. ...

A Global Pharmaceutical company are presently looking to bring on a Regulatory Labelling Consultant to be based in the UK West London Office, on a contract basis.

To assist with the activities relating to the Labelling Compliance Review.

Role:

- Generate country labelling differences, which have been identified though the labelling compliance review.
- Where required, review local labelling assessments to ensure compliance with Global Datasheet. ...

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

A leading Pharmaceutical Company are looking to bring on board a Senior Consultant to join their team in Berkshire.

To manage the RA CMC activities for the product line, including currently approved products as well as next generation products. To develop and manage regulatory submission strategies, in alignment with goals and timelines established by the product brand team and project teams. ...

A leading, global Pharmaceutical Company are looking to bring on board a Regulatory Affairs Clinical Trial Application Specialist, for a 6 month contract, to their site in Buckinghamshire.

Role:

- Responsible for managing regulatory aspects for assigned clinical trials (across Phase 1 - Phase 4 and spanning five therapy areas).
- Responsible for making sure the required regulatory intelligence is in place.
- Lead cross-functional teams. ...

An Internaitonal Pharmaceutical Company are presently looking to bring in a Regulatory Affairs Consultant to be based in their Swindon.

Job Purpose:

To manage all aspects of regulatory affairs relating to established products and contribute to the development and implementation of optimal regulatory strategies for development products and thereby ensure regulatory and commercial success for all markets outside the EU. ...

An interesting role has come up with a UK based medical device company for a Regulatory Affairs Associate. This is a great role for a regulatory affairs professional, looking to work with innovative devices on an international scale. Due to the variety within the role and the range of devices you will work on, you will be developing your career and gaining invaluable expertise on an international scale.

Start your week on a positive, and potentially career changing application! Apply today for a great Regulatory Affairs Specialist role with a developing medical device company based in Switzerland. There is great potential in this role for career development and skill enrichment, due to the training and supportive environment that the management provide. They are also offering a secure permanent role, with a good competitive salary.

A leading international pharmaceutical organisation is looking for a regulatory affairs executive to join their RA team in Cork . This is an excellent opportunity to get your foot in the door of a top company and gain useful experience for a 6 month contract. ...

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

Role: Regulatory Affairs CMC Senior Contractor
Duration: 6 months
Location: Homebased
Rate: £50 - £65 P/H

We are currently recruiting for two regulatory contractors to work on behalf of a leading pharmaceutical consultancy. They ideally need candidates who can start in the next month so they will be looking to arrange interviews over the next two weeks.

This is a fantastic opportunity for you to join one of the world's leading medical device companies and be based in the largest city in Switzerland.

Regulatory Affairs Manager (m/w)

Wir suchen für einen unseren Kunden – einem innovatives Pharmaunternhemen im süddeutschen Raum - einen REGULATORY AFFAIRS MANAGER mit mehrjähriger Erfahrung im Bereich der Zulassung. ...

Regulatory Affairs Officer, Biotech Company, CDI, Paris, France A successful and expanding CRO with a strong Biotech focus is currently looking for a Regulatory Affairs...

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

Regulatory Affairs Manager Belux – Brussels– Join a medium sized pharmaceutical Company with a great pipeline….!!! If you are looking for a strategic role for a pharmaceutical Company with a great pipeline, excellent share price and a culture of positivity and continual personal development then this could be the role for you. Contact Marc Van de Voorde on +41-(0)41-710.51.00 or +44(0)207 801 33 85 or alternatively send your CV to cv@advregulatory.com.

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

Director, CMC, Regulatory Affairs in Hertfordshire - Permanent. Shreeya Patel is recruiting a Director, CMC, Regulatory Affairs to join a global pharmaceutical company in Hertfordshire....

An outstanding opportunity to join one of the worlds leading contract research organizations and be part of a dynamic and growing international company. Join PRA as an Administrative Associate at our Moscow office, and help realize your career potential.

We are an international player on the medical devices sector and due to our continuous growth, we are looking to reinforce our QARA department (based inGhent) with a new talent.



Your responsibilities:



* · Ensure all the regulatory obligations within the R&D department
* · Preparing the files for submissions
* · Ensure the quality standards are met
* · General support activities to the business (audits, training, etc .. ...

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

An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA as a Local Regulatory Affairs Associate, and help realize your career potential.

The Director Regulatory Affairs is a visible and influential position requiring leadership, oversight and operational accountability for regulatory affairs strategy and execution. In the short term, this includes being hands-on in regulatory activities in support of clinical programmes. Longer term you will be accountable for developing a strategy that will form the basis of Marketing Authorization Applications (MAA)

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 work independently as well as within a regulatory sub-team

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 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 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 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 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 305 733 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 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 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 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

My client is global and one of the most reputable generics companies in the world, employing approximately 26,000 people across the globe. They have more than ten major global development centers and a worldwide network of more than 30 manufacturing sites, with a presence in more than 140 countries. I am recruiting for a Drug Regulatory Affairs Manager role to be based in Munich.

A fantastic and exciting Biotechnology company is looking to bring in a Director of Regulatory Affairs CMC on a permanent basis, to be based London.

My client is a manufacturer of sterilisation equipment. To work on chemical consumables such as biocides, chemicals and detergents.

Regulatory Affairs Officer

My Client, a leading Pharmaceutial company in Dublin is looking for a Regulatory Affairs Officer to Join there team for a 6 Month Contract. ...

My client, one of the Globes leading Biopharmaceutical companies is looking for a strategic and capable Regulatory Managers to join their International team.

Reporting to the Director of International Regulatory affairs you will be joining a team of regulatory experts, implementing and developing regulatory strategy in this exciting and rare opportunity. ...

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.

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. ...

Job Title: Regulatory Affairs Manager / Senior Regulatory Affairs manager / Senior Regulatory Affairs Associate / Reg Affairs Manager

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

Benefits: Generous annual salary + bonus + car + benefits

Are you working in Regulatory Affairs and tired of the daily grind ? If so then read on as a unique opportunity has opened up within a Specialist Pharmaceutical Company who are seeking a Regulatory Affairs Specialist to be based in London. ...

Gold Group is seeing a significant increase in activity in the Regulatory Affairs arena within the Pharmaceuticals and Device market and below you will see a snapshot of the opportunities I have available.

(31196) Reg Affairs Director – London - £80,000– £90,000 - Perm
We are looking to experienced Director to provide strategy and expert advice within the biopharmaceutical industry. ...

A Leading Global Pharmaceutical Company are presently looking to bring in a Regulatory Affairs
labelling consultant to be based in their West London Office.

To assist with the activities relating to the Labelling Compliance Review. Deliver to time and quality targets as defined by the project.

• Generate country labelling differences, which have been identified though the labelling compliance review. ...

Key Responsibilities:
•?Publishing and dispatching submission dossier in various format
•?Updating submission registration information and tracking submission progress
•?Ensuring assigned submissions to be properly quality checked and all findings to be properly
addressed
•?Leading assigned major submission publishing projects with designated publishers
o Working closely with functional group for submission timelines and timely
document deliverables for submission ...

My client is a small yet growing, highly reputable and very successful, Regulatory and Pharmacovigilance focussed consultancy based in the Berkshire/Buckinghamshire area. What distinguishes this client from other consultancies is their distinct focus on team work and personal development, with the directors truly believing in offering each and every employee the chance to develop on both a personal and professional level.

My client, a regulatory consultancy is looking for a regulatory advisor to join their team to work as a regulatory advisor on their pharmaceutical team. This position will be based inTipperarybut some travel will be required.

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 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 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 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

My client is a large global pharmaceutical company based in France with a large successful portfolio of products currently on the market and in development. The EU Headquarters has a large regulatory function which is the global hub and is currently seeking a Director of Regulatory Affairs to manage the Emerging Markets division.

We are currently looking for a specialist in medical device regulatory affairs to act in the capacity of Authorised Representative for an on behalf of their European Medical Device legal authorisations.

An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA as a Regulatory Affairs Associate and help realize your career potential.

Working within this great company, you will have the opportunity to work on a variety of projects, from non clinical, clinical and post marketing activity, including small molecule, large molecule, medical devices and occasionally even veterinary products.

Senior Reg role working for a gloabal pharma company with an exciting pipeline. Excellent team environment and great experience to be gained.

My client is an expanding & developing research company with an office located in Cambridge. This is an fantastic opportunity for an experienced Regulatory Affairs professional to join a vibrant, dynamic & experienced regulatory affairs team in a company with an excellent reputation in the industry internationally.

Job Title: Senior Regulatory Affairs Manager Salary: Up to £80,000 + Package Location: Oxfordshire Business Type: Speciality Biopharmaceutical company

Associate Director of Regulatory Affairs - Permanent - Hertfordshire Shreeya Patel is recruiting an Associate Director of Regulatory Affairs to join a global pharmaceutical company at...

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

Just Pharma are currently working on behalf of a niche organisation within the Pharmaceutical sector located in the Cambridgeshire region looking for experience Regulatory Affairs professionals interested in a new challenge. My client has various opportunities available being offered at varying levels of seniority.

Las actividades pueden llevarse a cabo preferentemente desde Alemania o en México en caso de encontrarse en el país.

El objetivo de la posición principal es el prestar el servicio de consultoría, desde el punto de vista regulatorio, al cliente que busca ingresar en el mexicano de dispositivos médicos.

My Client, a leading Medical Device Company are looking for a Regulatory Affairs Specialist for a 6 month contract. The role will be based in Athlone. The position offers an attractive daily rate. ...