The latest Regulatory jobs - BETA

Superb role for an accomplished Regulatory Affairs Director/Senior Director with expertise in Biologics and Biosimilars. A Biologics/Biosimilars background is essential for this role, along with Line management and an EU perspective. EU/Global Regulatory Strategy and full pipeline working knowledge. Based in the UK or France.

My client is looking for a Senior Regulatory Affairs Consultant to join their growing team. You must have a good amount of previous experience in Regulatory Affairs and CMC/Quality and/or non clinical and clinical aspects.

Contract opportunity available for RA professionals familiar with preparation and submission processes throughout the product lifecycle.

Job title: Clinical Trial Regulatory Leader
Job type: 6-12 month contract + extensions
Location: High Wycombe, Buckinghamshire
Salary: ÂŁ30 to ÂŁ35/hour contract rate

A Clinical Trial Regulatory Coordinator with substantial pharmaceutical regulatory affairs experience is required by a leading pharmaceutical R&D company based in the High Wycombe area
The ideal candidate will be responsible for leadership of CTAs throughout product lifecycle, as well as development of CT ...

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!

Regulatory Affairs Officer, CDD, Biotech A niche and successful CRO with a strong Consultancy Arm and focus on the Biotech industry is currently looking for a...

Senior CMC RA Specialist for a fast growing Pharmaceutical Brand in Central Switzerland

Role: Regulatory Affairs CMC Senior Contractor
Duration: 6 months
Location: Homebased
Rate: ÂŁ50 - ÂŁ65 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.

A pharmaceutical company based in the South are seeking a number of Regulatory Publisher urgently, on an interim basis for a 6-12 month contract.

CMC Expert, Range of Therapy Areas, English Speaking, Variation between QA and Regulatory Departments, Zug

Become the CMC expert/ go to person for CMC for an upcoming start up company with a number of established products on the market. The role will be focused on submissions and writing for CMC for the FDA. Due to this being a smaller company your duties will be broad from mentoring junior staff to coverage of change control, aspects in QA and working closely with supply chain.

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 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.

Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for providing delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and review and finalization of essential documents required for site initiation.

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.

Great Regulatory opportunity for a European Senior 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 ÂŁ42,000 is offered plus leading benefits. Essex location.

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. ...

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...

A new contract opportunity has arisen with a leading pharmaceutical company based in Buckinghamshire. Our client are looking for an experienced Regulatory Contractor with strong labeling experience to join their team on an initial 6 month contract. Applicants must be able to display sound knowledge and good competency with global labeling activities for established products. Buckinghamshire location.

Snr Regulatory Affairs Manager - Top 15 Pharma

Looking for the next step up in your career? Want to work for a multinational organisation? This could be the opportunity for you.

Senior Regulatory Affairs Assocaite role working for a gloabal pharma company with an exciting pipeline. Excellent team environment, gain great experience

Clinical Study-Start up Specialist, Study Start-up, Regulatory Submissions Manager / Study Start-up Project Manager – SCOTLAND part home based Please contact Zoe Benningfield on 07896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential. Clinical Project Manager, Clinical Study Manager, Regulatory Submissions Manager , Study Start-up Project, Site set-up, Study start up specialist.

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. ...

My client is a specialist biotech company working within the field of Oncology drug development. They are currently turning a corner and lead compounds are entering clinical phases. As such, my client requires a Regulatory Leader level freelance consultant that can offer add-hoc support with pivotal regulatory activities. ...

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

Associate Director Regulatory Policy and Intelligence opportunity has arisen with a leading Research based Biotherapeutics Company in the South East on a permanent basis with an excellent salary and benefits package on offer. This is a highly visible role with regular liaison with internal cross-functional departments and external Regulatory Agencies and associations.

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 .. ...

An excellent opportunity has arisen to join one of the world’s most prestigious pharmaceutical companies based in Switzerland. Working on a 70% basis our client is looking for someone to join their Therapeutic Area in Ophthalmology and Neuroscience. ...

This is a new opportunity for an expert in Regulatory Early Development to lead early phase projects in a leading international pharmaceutical company in Switzerland.
This position is to lead regulatory contact and expertise for assigned Therapeutic areas from Candidate Selection through to POC/DDP. ...

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 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

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

Regulatory Operations and Publishing Specialist - excellent package!!
Our client is a Top Company and seeks a Regulatory Publisher with approximately 3+ years experience. The candidate will have a broad-based knowledge of Regulatory Operations and Publishing across the EU and ideally, Globally.

Regulatory Operations and Publishing Manager - excellent package!!
Our client is a Top Company and seeks a Regulatory Publisher with approximately 5+ years experience. The candidate will have a broad-based knowledge of Regulatory Operations and Publishing across the EU and ideally, Globally.

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.

INC Research will be recuiting for a Site Start Up and Regulatory Specialist in the near future. Please apply so that you can be considered when the position is live.

A medical regulatory advisor acts as liaison for medical information to internal and external stakeholders, and is responsible for;

• Ensuring regulatory requirements for new and existing products are met

• Providing the medical, non-promotional, information in regard to products to customers in order to ensure safe & effective use

• Providing scientific support to the other internal department (Marketing/Field Force) for the relevant therapeutic area

• Me ...

Superb role for an accomplished Regulatory Affairs Director/Senior Director with expertise in Biologics and Biosimilars. A Biologics/Biosimilars background is essential for this role, along with Line management and an EU perspective. EU/Global Regulatory Strategy and full pipeline working knowledge. Based in the UK or France.

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