The latest Regulatory jobs - BETA

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.

A fantastic and exciting specialised Regulatory Affairs consultancy company is looking to bring in a Director of Regulatory Affairs, to be based in the South East of the UK.

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.

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.

Prestigious global pharmaceutical company requires a CMC professional to drive global regulatory strategy for medical devices & combination products throughout the product lifecycle, with a focus on creativity and innovation.

Prestigious global pharmaceutical company requires a number of CMC professionals to drive global regulatory strategy for development projects and/or marketed products throughout the product lifecycle, with a focus on creativity and innovation. All positions are permanent.

Our client is a mid sized Pharmaceutical company looking for an experience Senior Regulatory Affairs Manager to join their expanding team for permanent role in the Cambridge or Limburg area. This opportunity is available for an enthusiastic and driven individual to join the European Regulatory team with a responsibility for the Pain therapeutic area.

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.

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.

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

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. ...

Due to plans to expand into new markets this exciting and highly intelligent business now needs a Regulatory Specialist to aid the completion of 510k submissions and product registrations.

Working closely with the RA/QA manager, the successful individual will be completing regulatory activities that are essential for the business to move in to a possible two new territories.

General Responsibilities Include;

* Completing current 510k submissions. ...

Head of Regulatory Affairs - Strategic Role- Live Abroad

Looking for career progression? Looking to make your mark? This could well be the opportunity for you. A relatively young company, who are expanding exponentially are looking for someone to Head up their Regulatory Affairs department in Prague, Czech Republic.

Senior Regulatory Operations and Publishing Specialist - 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.

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.

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. ...