The latest Regulatory Affairs / Reg affairs jobs - BETA

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. ...

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 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.

The RA Associate’s day to day activities will include;

* Work closely with process development teams to integrate Safety Assurance activities into product development processes
* Construct Safety Assurance Case for Product offerings
* On-going maintenance of Safety Assurance Case
* Construct and maintain the Risk Management File
* Liaise directly with FDA and government agencies to ensure structure and management of the Safety Assurance case is as expected. ...

Interim role for Director level Regulatory Affairs Professional.

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

A Leading Global Pharmaceutical Company are presently looking to bring in a Regulatory Affairs Consultant to be based in their Weighbridge office.

Work closely with product development, manufacturing and other functions on key projects designed to release value back into the organisation whilst maintaining product quality, safety and efficacy.
Will involve looking at change controls to products, packaging and raw materials. ...

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

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

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 / 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 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 / 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 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

My client, a leading animal health company is looking for a regulatory affairs specialist to join their regulatory affairs team as the Russian specialist. The regulatory affairs specialist will be based on site in Co Meath. The company is based in over 128 countries and has 32 manufacturing plants globally.

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

This is an fantastic opportunity to join a leading Bio-pharmaceutical company in their EU development team. You would be working on our clients impressive pipeline...

A Leading Global Pharmaceutical Company are presently looking to bring in a Regulatory Affairs CT Consultant to be based in their High Wycombe.

This position is responsible for managing / assisting in all regulatory aspects for Phase 1 – Phase 4 clinical trial authorization applications conducted globally, regionally or locally, spanning all Therapeutic Areas. Working under the Clinical Trial Application Coordination group, reporting to the Director. ...

I have a fantastic opportunity for a Drug Regulatory Affairs Manager role for my client who are a global leader in the development of generic drugs. Both permanent and contract roles available to be based in Munich. This is an ideal opportunity to expand your regulatory experience within a world class environment.

To apply for this regulatory affairs consultant 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 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 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 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

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

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 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. ...

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. ...

Business type: Generics company This is an exciting opportunity to join an industry leading generics company, working with a variety of therapeutic areas and taking control if all regulatory operations for Europe.

My client is one of the worlds most respected & successful pharmaceutical companies. They are currently looking for a Regulatory Affairs Manager to join their team in Maidenhead. This is a rare opportunity to join one of the industries most innovative companies! An opportunity not to be missed for any experienced Regulatory Affairs Professional! Want to know more?

This market leading company is looking for a Regulatory Affairs officer to Join their Regulatory Affairs team for a 6 month contract. ...

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. ...

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

Regulatory Affairs Specialist

Are you ready to take that first step of your career into a global role? I am urgently looking for a regulatory affairs specialsit for a multi-faceted role in one of the best global Medtech companies in the world! The successful candidate will enjoy an excellent salary and relocation package, along with one of the most interesting jobs in a beautiful area of Switzerland- Zurich.

A Global Pharmaceutical company are presently looking to bring in a Regulatory Affairs, Labelling Manager to be based in their Surrey Office, on a contract basis for 12 months.

Role:

- Responsible for executing the content management of local product documents.
- Updated on regional labeling regulations.
- Oversee content across all labels.
- Responsible for the production of labels, Language Documents, Patient Information Leaflets and any Technical leaflets. ...

Contract / Interim Regulatory Affairs Manager

Lawrence Harvey Pharma is currently working with a leading biotech company who require a Regulatory Affairs Manager on a contract basis. The company profile discovers, develops manufactures and delivers innovative human therapeutics.

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

This role comes with direct reports, a car allowance and a very competitive salary. The project work is CMC focused but varied and covers development and marketed products. 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

The salary is up to £33,000 for the right candidate and your team will be led by an experienced and highly rated Regulatory Manager who has an outstanding reputation in the Industry for training and development. 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 role please call Julie Cooper on 020 8305 9733 or 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk

This is great role with enough scope to keep you interested and enough development opportunities to allow you to continue to grow as a regulatory professional. 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

I have a fantastic opportunity for a Regulatory Affairs Manager to join a leading pharmaceutical consultancy firm in Essex on a permanent basis. You will be covering every aspect of regulatory affairs as it is a broad role with a variety of key responsibilities. My client is offering a competitive salary package along with benefits and a chance to expand your regulatory experience within a dynamic and forward thinking company.