The latest Regulatory Affairs / Reg affairs jobs - BETA

Job Description



A Southern California, California based Class III medical device company is seeking a Manager of Regulatory Affairs. The Manager will have responsibilities to support the product in the EU as well as assist/prepare submissions in theU.S.and other international markets. The ideal candidate will have experience with IDE and PMA submissions.

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. ...

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

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

Head of Regulatory Affairs - European Experience

Tired of the UK? Looking to branch out and gain international experience? This could be the opportunity for you!

Our client are looking for a Regulatory Affairs Manager to join their company at a point of growth and development. Our client are a start-up medical device company based in Germany, that are progressing with a new and innovative range of devices. Through the small knit nature of the company, as the regulatory affairs manager you will get the opportunity to be part of company wide decisions; and make a real change on the development of this medical device company.

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 to work in a leading biologics department at the heart of a global pharmaceutical company. In this position you will have a significant role in the preparation and submission of documents from early development to post approval in CMC. In addition to this, there is a strong emphasis on international submissions.

Regulatory Affairs Labelling Specialist - EU Experience

My client, a top 20 Pharma, has an opening for a Regulatory Affairs Specialist to join the team. This is an opportunity to expand your current experience and knowledge in terms of EMA labelling regulations which in turn will give your CV a great boost. Although the focus is Europe there will also be work needing completion on a global scale thanks to my client having offices in 32 countries.

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 Manager, CMC, Technical and Strategic input, Global Pharmaceutical Company working on products in development and established brands

An excellent opportunity to join a very successful and well developed pharmaceutical team working on regulatory affairs for a strong product pipeline in Oncology. Great opportunity to further your career in regulatory affairs working on challenging CMC documentation and submissions.

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. ...

Have you always wanted to have a life changing impact, developing devices that will affect a patient's life? This unique and new role as Regulatory Affairs Manager, would give you the opportunity to be directly involved in bringing innovative, life enriching devices to market on an international scale. The role is based in Germany, with a great salary package offered.

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...

Global Snr Regulatory Affairs Manager - Immunology

My client is looking for someone to join their worldwide corporation in London. This is a chance to work on their entire 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.

A Senior Regulatory Affairs Manager is required for a reputable mid sized pharmaceutical company for a permanent role in either the Cambridge,UK or Limburg, Germany location. They specialize in a niche product market and are 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.

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.

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 a Local Regulatory Affairs Associate and help realize your career potential.

Fantastic opportunity at Director level with a highly respected pharmaceutical company based in the North Home Counties. Highly visible position which would have responsibility for both development and established products. Must have very strong technical regulatory experience and be able to display excellent competency in both project and people management. Good location accessible from a number of locations with a company that has an excellent reputation within the industry.

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

The medical device industry, is developing as the exciting and interesting market to be working in within the health care industry; due to the changing and developing regulations. Take the opportunity with this Regulatory Affairs Associate role, to work for a market leading medical device company based in a great London location. Our client are looking to take on someone they can develop within their company, allowing to develop your career within regulatory affairs.

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.

This is an excellent company who offer flexible working hours, excellent career development and a friendly working environment.

This Global Pharma have the best retention rate out of any clients we work with (8 out of the top 10 pharma + smaller companies also).

You will be part of a brand new growing departments that is being built in the UK in their European headquarters.

Bearbeitung von Zulassungsverlängerungen Uebernahme von ausgewählten Produkten für den CMC-Teil Erstellung bzw. Bearbeitung bei Änderungen gemäss der aktuellen regulatorischen Anforderungen Kontaktpflege mit Behörden, dem deutschen Mutterunternehmen und internationalen Herstellern aktive Zusammenarbeit mit internen und externen Stellen

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

Labelling Manager - Regulatory Affairs - Training

My client is looking for a relatively inexperienced professional to join its Regulatory Affairs team. With a promise of training and development this job opportunity is for those who wish to progress their career into line management. With 6 direct reports over 2 countries this will give your CV great added value, making your porgression easier in the future.

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

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

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.

To apply for this regulatory affairs officer 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.

This role could be for 6 or 12 months (your choice) and you will be joining a well-run and friendly team in role with lots of autonomy and strategic input - My client is also happy to wait for a 1 month notice. 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

Associate Director Regulatory Affairs Emerging Markets opportunity has arisen with a leading Global BioPharmaceutical company on a permanent basis in the South East. My client's Regulatory emerging markets department is rapidly expanding as they continue to develop their exciting portfolio globally.

A Fantastic opportunity has arisen to join an award winning health care service provider in their Regulatory department with a range of responsibilities on a European and Global level. ...

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

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

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. ...

My client is an award winning Medical Device Company who have leading products within multiple fields. They are now looking to strengthen their European Regulatory team with the appointment of their newest RA & QA Manager to be based in Southern Germany. This is a combination role that requires substantial experience in both disciplines with leadership skills also being critical for the successful candidate.

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 in Tipperary but some travel will be required.

A position is vacant in the Otsuka Group Regulatory Affairs Department. The successful candidate will be placed in London (UK) as a Regulatory Affairs Specialist (m/f)

Eine einmalige Chance einer Organisation beizutreten, welche Frauen weltweit verbindet, durch einzigartige und innovative medizintechnische Produkte Linien. Es ist eine kleine, jedoch eine wahrhaft globale Firma mit Herstellern in der Schweiz, den USA und einer Präsenz in 3 verschiedenen Kontinenten.

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

JOB SCOPE/PURPOSE
• Co-ordinates the preparation of regulatory submissions for the Programme for Registration of Established Products (PREP) and any related RTQs for delivery to LOCs in Emerging Markets and Asia Pacific Region (EM&AP) and specific European Markets. ...

A new opportunity has come up within a CRO looking for a regulatory affairs executive to join their expanding team.

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.

One of the world's leading companies with >26,000 employees in 90 countries dedicated to the purpose of bringing plant potential to life. Through world-class science, global reach and commitment they are able to increase crop productivity, protect the environment and improve health & quality of life.

To apply for this regulatory affairs manager role please call Julie Cooper on 020 8305 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 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 small niche biotechnology company who is seeking a Director Regulatory Affairs to manage the regulatory operations on a global level. You will report to the VP of the Regulatory group and hold significant regulatory experience on a international level. Ideally you will have gained experience working with innovative products (biologic) and previous leadership/managerial experience.

Senior Manager, Regulatory Affairs - Permanent - Oxfordshire Shreeya Patel is recruiting a Senior Manager, Regulatory Affairs to join a small yet well established speciality US...

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

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

My client invests heavily in talented teams as this is central to their ambitious expansion plans. ...

Regulatory Manager



Suchen Sie aktuell nach einer neuen Herausforderung im Bereich Regulatory Affairs?



Für einen Kunden hier in der zentral Schweiz suche ich aktuell nach einem Regulatory Advisor.



Diese Position ist direkt dem Medical und Regulatory Affairs Manager unterstellt und berichtet in wöchentlichen Meetings direkt an ihn. ...

Your responsibilities will include:
converting labelling documents and International Package Inserts to new templates and conducting a content compliance check for consistency. ...

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. ...

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 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 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 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

The salary for this role is up to 145,000CHF with a bonus and extensive re-location 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 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100

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

There is an excellent salary available for this role (up to 110,000 Euros) and this position also offers a fully expensed Car, Attractive Bonus, Shares and a Full- Re-location 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 UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100

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 your CV to: julie@mosaicrecruitment.co.uk

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 CMC Regulatory affairs role please call Julie Cooper on 0208 305 9733 or 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk

A leading innovative pharmaceutical company based in Buckinghamshire is recruiting for a Head of Regulatory Affairs to be based in Buckinghamshire.

My client, a global generic pharmaceutical company in Tipperary is looking for a Regulatory Affairs Officer to join the Regulatory Affairs team.

The regulatory affairs officer will be working directly with the regulatory affairs manager and will be the sole point of contact within the department in their absence.

Senior Regulatory Affairs Executive - Leading Global Pharmaceutical Company - London based - Up to £40,000

Senior Regulatory Affairs Executive - Leading Global Pharmaceutical Company -Londonbased - Up to £40,000

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 Executive to join their team inLondon.

A Leading Global Pharmaceutical Company are presently looking to bring in a Regulatory Affairs Registration Manager to act as a Consultant and be based in their Brussels Office.

Daily tasks will be related to the regulatory management of products. Role will be to project manage filing of variations worldwide including Europe and resolve supply related issues. It may involve both maintenance of dossiers as well as new dossier submissions. ...

Regulatory Affairs Manager (Zurich, Switzerland, New product development, devices, RA)

Job title: Regulatory affairs manager

Location: Zurich, Switzerland

Salary: CHF base (130,000-145,000)

Contact: Elena.kyriacou@huntressgroup.com call: 0044 207759 7790

I’m searching for Senior Regulatory Affairs Associates to work for a global specialty pharmaceutical company. Based in the West Midlands

Within this role your main areas of responsibilities will include the following areas:

• Project management of European (MRP’s, CP’s, NCE) and World-wide regulatory projects.
• Preparing registration strategies as appropriate.
• Provide advice and determine appropriate action for proposed manufacturing/license changes. ...

To apply for this regulatory affairs coordinator 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 CMC 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 020 8305 9733 or 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk

To apply for this regulatory affairs food supplement 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 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 CMC 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 020 8305 733 or 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk

A thriving Consultancy based in Cambridgeshire is currently searching for a
Senior Regulatory Affairs Consultant who can provide advice within the pharmaceutical industry.

The ideal candidate will have a minimum of 5 years’ UK Pharma experience in the development of pharmaceutical and biotechnology products and is already working in regulatory affairs. ...