The latest Regulatory jobs - BETA

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 £42,000 is offered plus leading benefits. Essex location.

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 £42,000 is offered plus leading benefits. Essex 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.

Regulatory Affairs Manager – Belgium - Antwerp

Join this fast paced and dynamic top 5 global CRO for a permanent contract and gain great exposure to EU Regulations.

Job Title: Regulatory Affairs Manager / / Regulatory Affairs Executive
Location: Antwerp / Belgium / Antwerpen
Benefits: Competitive salary package

Job Responsibilities:
• Provide expert regulatory advice and ensure accurate compilation, management and tracking of submissions. ...

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.

Regulatory Affair’s Associate – 9 Month Contract.

Reporting to the Regulatory Affairs & Compliance Supervisor, you will be responsible for the regulatory procedures and processes in compliance to FDA QSR’s, Medical Device Directive 93/42/EC, ISO 13485 and internal requirements to support the IOL Production for an 9 month period. ...

Would you like the option to work a permanent or 12 month fixed term contract for a stable pharmaceutical company in either the Cambridgeshire area or in Germany? Are you looking for a management role in Regulatory Affairs with career growth potential in a rapidly expanding niche product company? Than this may be the right role for you!

Regulatory Affairs Consultant - Top Consultancy

My client, a high end regulatory affairs consultancy, is looking to add a new consultant to it's team. The very nature of a consultants work is varied and flexible meaning you will receive incredible job satisfaction thanks to the possibility of working on multiple projects and case studies.

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.

A global pharmaceutical company are looking to bring in a Regulatory and Development Manager to work on Animal Health products, based in Berkshire

Job Title: Regulatory Affairs Operations Assistant / Reg Ops Assistant / Regulatory Publishing Assistant / Regulatory Affairs Publisher

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

Benefits: Generous hourly rate and solid training

Excellent opportunity for a Regulatory Manager to progress their career in a world leading pharmaceutical company. This newly created position would be responsible through the full regulatory cycle, form development to registrations and post approval activities. Highly desirable company and location. Excellent salary and benefits.

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

Gain management expertise and be part of company wide decisions, with this great Regulatory Affairs Manager role. Our client are a start-up company based in the North of Germany. They specialize within innovative and new technology medical devices. Not only is this a great role to develop your management expertise, you will gain an interesting and varied working life. They are also offering a competitive salary package.

Role: Regulatory CTA Consultant
Duration: 6 months
Location: High Wycombe
Rate: £30 - £35P/H

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.

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.

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: £30 to £35/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: £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.

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.