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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Regulatory Affairs - Become a Specialist - Galway
Galway
Aug 30
Are you in the beginning of your career in Regulatory Affairs, looking for the best next step to build a successful professional path? This is your chance to become a Regulatory Affairs Specialist and join a global company, the right environment to develop as a professional.
Regulatory Writing Manager
Los Angeles
Aug 30
Job Description:



* Independently writes clinical study reports, Investigator Brochures, Summary of Clinical Efficacy, Summary of Clinical Safety, Summary of Clinical Pharmacology, Summary of Biopharmaceutics, Clinical Overview, Table of All Studies, briefing documents, Risk Management Plans, Response to regulatory questions
* Participates in document development for FIH studies
* With supervision, as appropriate, writing Module 3 and 4 documents for CTD
* Writ
Regulatory Affairs Specialist-Great Work/Life Balance-Devices
Lyon
Aug 29
Gain a great work/life balance with this regulatory affairs specialist role in France. This is a great opportunity to develop a regulatory affairs career with a world leading medical device company. Our client are supportive in the development of regulatory affairs professionals and are looking to take on a regulatory affairs specialist to develop and train within innovative class III implantable devices. Apply now to find out more.
Senior Regulatory Affairs Manager-Cross Function Role-Devices
Zürich
Aug 29
Are you a regulatory affairs professional within the medical device industry looking for a varied role? Apply now for this senior regulatory affairs manager role which will see you leading a varied and interesting working life. Within this regulatory affairs role you will gain a great deal of cross-function work within quality. Apply now to find out more about our market leading client within the medical device industry with this exciting role in regulatory affairs.
Regulatory Submissions Manager (m/w)
Munich (County)
Aug 29
Regulatory Submissions Manager (m/w)

Für unseren Kunden, ein internationales und mittelgroßes Auftragsforschungsunternehmen suchen wir einen Regulatory Submissions Manager (m/w), office-based im Herzen von München. Es erwartet Sie ein internationales Team, zahlreiche Entwicklungsmöglichkeiten und ein sehr gutes Betriebsklima. ...
Regulatory Affairs and QMS Manager-Futuristic Devices-Switzerland
Basel
Aug 29
NonStop Recruitment are currently sourcing for on behalf of our client, a market leader within the medical device industry a regulatory affairs and QMS manager. This is a great opportunity for a regulatory affairs and quality assurance professional to work with internationally leading and innovative medical devices. The medical devices our client register are futuristic in their design and technology, be part of the future with this company! Apply now to find out more.
Regulatory Project Manager – EU Locations, or Home Based
Germany
Aug 29
A fantastic opportunity has become available, working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level, this company invest heavily to attract and retain high quality staff; this organisation has a very credible reputation for being one of the best employees in its arena. My client invests heavily in talented teams as this is central to their ambitious expansion plans.
Regulatory Administrator - Entry level - Yorkshire
South Yorkshire
Aug 29
We currenty have an opportunity for a regulatory administrator to join a pharmaceutical company in Yorkshire and gain skills to carry you through the regulatory field.
Regulatory Project Manager – EU Locations, or Home Based
England
Aug 29
A fantastic opportunity has become available, working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level, this company invest heavily to attract and retain high quality staff; this organisation has a very credible reputation for being one of the best employees in its arena. My client invests heavily in talented teams as this is central to their ambitious expansion plans.
Regulatory Affairs Manager Flu – The Netherlands
Netherlands
Aug 29
Opportunity to join a leading pharmaceutical company in their office based in the Netherlands.
Contract - Regulatory Affairs Manager Flu – The Netherlands
Netherlands
Aug 29
Opportunity to join a leading pharmaceutical company in their office based in the Netherlands.
Project Manager/Senior Project Manager – Regulatory Affairs
France
Aug 29
A fantastic opportunity has arisen to join an award winning health care service provider in a home based project manager role. They provide drug discovery, development and lifecycle management services and have presence globally. Their clients and partners include pharmaceutical, biotechnology, medical device, and academic and government organizations.
Senior Regulatory Affairs Manager
England
Aug 29
An exciting new opportunity has arisen for an experienced Senior Regulatory Affairs Manager to join a leading pharmaceutical company in London.
Senior Regulatory Affairs Intelligence Manager - URGENT
West London
Aug 29
My client is a multinational biotech company based Uxbridge. They are seeking a Senior RA Manager on a rolling 12 month contract. The desired individual will have extensive experience in gathering intelligence and providing regulatory strategy ideally in the emerging markets.
Associate Director, Regulatory Affairs - Oncology
England
Aug 29
An exciting new opportunity has become available for an Associate Director to join a leading Pharmaceutical organisation in London.
Regulatory Affairs Manager - Established Products
England
Aug 29
A fantastic and immediate need has arisen at a global pharmaceutical company for a Regulatory Affairs Manager to join the team. You will be responsible for Established Products within your designated therapeutic area (CVM) My client is a research-based global pharmaceutical company, and is amongst the leading pharmaceutical companies in the world.
Senior Regulatory Manager, Great Company Culture
North West England
Aug 29
An internationally renowned firm with a vast portfolio of products is looking for a Regulatory Affairs Manager to act as the SME for one of major product ranges of borderline products. The company has developed an exciting range of devices that border regulations between the Medical Device and Cosmetic industries. The company has a fantastic company culture with flexible working hours and some working available.
Senior Regulatory Associate, Great Development
Central Belt
Aug 29
A top medical devices manufacturer of award winning innovative Class III products has a position open for a Senior Regulatory Affairs Associate. The site is based in the scenic West Coast of Scotland, half an hour from not only a vibrant city centre but also a national park and Coastal paths. The company has undergone a massive recruitment drive over the last few years and looks set to become the industry leader in its product sector in the not too distant future.
Regulatory Affairs Specialist - FDA
Dublin
Aug 29
Regulatory Affairs Specialist - FDA

Develop FDA experience whilst also gaining EU and Global experience as a Regulatory Affairs Specialist. This position gives you the opportunity to gain skills in areas that will broaden your skills and allow you to become that much better than your competition.
Associate Director Regulatory Affairs - Germany
Frankfurt am Main
Aug 29
One of Germany's top employers and at the same time one of the strongest global pharmaceutical companies is currently looking for a strategic focused associate regulatory affairs director. This is an exceptional opportunity to get involved in regulatory affairs for an industry leading company which unlike other global giants believes in taking control of projects and having full ownership, as opposed to having you pidgeonholed into a very narrow field. ...
International Regulatory Strategy Lead
Hampshire
Aug 29
International Regulatory Strategy Lead
Permanent Role
Competitive negotiable salary + bonus and benefits
Based in Hampshire, UK
Contact me ASAP: Mariam@secpharma.com or 02072556665
Regulatory Affairs Specialist, Medical Device – Bern, Switzerland – upto 120,000 CHF
Switzerland
Aug 29
I am currently working with one of the world’s leading Medical Device organisation with a wide variety of innovative Medical Device products and medical technologies working across multiple therapeutic areas. A true global leader within their field and they are always expanding the countries they operate in and distribute to.
French Speaking Regulatory Associate
Kent
Aug 29
An opportunity has arisen within a Consumer Health client, who has ambitious plans to take their business to the next step. This position is highly integral to them achieving these business objectives.
Regulatory Affairs Specialist - 6 Month Contract
Inverness
Aug 29
6 Month Contract, Scotland, Regulatory Affairs, Medical Devices, IVD, CE Marking, FDA, Lifecycle, Labelling, Variations
Senior Regulatory Associate - OTC/Consumer Health
Berkshire
Aug 29
As one of the leading businesses within the Consumer Health market, this opportunity is one not be missed!

You will report into the Regulatory Affairs manager and undertake all work necessary for the business to remain in constant compliance with all local regulations.
Global Head of Regulatory Affairs
New Jersey
Aug 28
A rapidly growing pharmaceutical organization focused in the area of neuroscience is seeking to hire a Global Head of Regulatory Affairs. This role will sit...
Regulatory Affairs Specialist - Ireland
Dublin
Aug 28
Regulatory Affairs Specialist - Ireland

Apply now for the opportunity to work as a Regulatory Affairs Specialist for a company that is in the Top 5 largest generics company in the world today. Work with a successful organisation that ensures job security giving you the chance to grow and progress within the industry.
Regulatory Affairs Specialist/Associate – Medical Devices – New York/New Jersey
New York/New Jersey area – office based
Aug 28
Regulatory Affairs Specialist/Regulatory Affairs Associate: This is an exciting opportunity to join a large and growing Medical Device company in the New York/New Jersey area. You will be working on a range of strong products already on the market with a friendly and fast paced office.
Regulatory Affairs Specialist-Pharma Company
Slough
Aug 28
My client, an international recognized pharma company, is looking for a Regulatory Affairs Specialist to join their Regulatory Affairs department in Berkshire UK.

As a Regulatory Affairs Specialist you will be responsible of the submissions, redaction and registration of documents in UK and Ireland. You will support the Global Regulatory Affairs (GRA) department in order to deliver strategic and operational regulatory plans and activities. ...
Director Regulatory Affairs – Teamverantwortung – Hamburg
Hamburg
Aug 28
Als Director Regulatory Affairs sind Sie für die Betreuung der Zulassungsabteilung zuständig. Sie leiten das Team und koordinieren die Tätigkeiten des Teams. Weiterhin arbeiten Sie an der strategischen Ausrichtung der Abteilung und Sie sind für die Planung von Zulassungen verantwortlich. Außerdem repräsentieren Sie das Unternehmen bei den Zulassungsbehörden und implementieren rechtliche Vorgaben.
Regulatory Consultant- Urgent 3 month contract -Immediate Start
Cambridge
Aug 28
A leading CRO, based in Cambridge are looking to take on several Regulatory Affairs Consultants with good knowledge of Regulatory Affairs, on 3 month contract. They are looking for someone with at least 6-12 months knowledge of Regulatory Affairs. This contract is likely to extend past 3 months.
Head of Regulatory Affairs and QMS-Be the Lead-Devices-Zurich, CH
Zürich
Aug 28
Be the next lead within the regulatory and quality department of a global medical device company based in the greater Zurich area. If you are looking for your next managerial role within regulatory affairs and quality assurance this is the role for you! As the head of regulatory affairs and QMS you will manage the full product life cycle. Apply now to find out more and be the next manager of a global medical device company!
Senior Regulatory Consultant – CMC
Hatfield, Hertfordshire
Aug 28
A full time 6 month contract based in Hatfield, for 37.5 hours per week at £60.00 per hour.Exciting opportunity to work with a top Pharmacutical organisation that has an innovative portfolio of products including biologics and small molecules. You would be a pivotal team member, representing CMC at a senior level and contributing to management reporting. The ideal candidate will have previously worked with oncology products and be a CMC specialist.
Regulatory Affairs for Devices – Germany: OVER 20 POSITIONS
Germany
Aug 28
Are you a Regulatory Affairs professional looking for Regulatory Affairs opportunities in Germany? Please find a list of some roles that could be a great fit for you!
Regulatory Affairs for Medical Devices in Germany CLICK HERE
Germany
Aug 28
Are you a Regulatory Affairs professional looking to keep their options open? Are you actively looking for interesting roles? My name is Mahdi Chab and I am a specialist Headhunter in the field of Regulatory affairs for medical devices....
Regulatory Affairs - Huge Growth
South Yorkshire
Aug 28
Regulatory Affairs - Huge Growth

Apply to work as a Global Regulatory Affairs Associate for a Global Organisation who are spending millions for a new centre. This is the place to be, join and grow with a company that is making noise in the market. Not only will you obtain new skills but it will make your CV from average to reputable.
Regulatory Affairs: Medical Devices Join our network
Germany
Aug 28
Are you a Regulatory Affairs professional looking for Regulatory Affairs opportunities in Europe? Are you looking for someone to represent you that can offer you Regulatory Affairs positions based on your background, skills and interests? Then look no further!
Associate Director Regulatory Affairs - UK or Germany
UK, Germany
Aug 28
Planet Pharma are looking for an Associate Director of Regulatory Affairs to be based either in the UK or Germany. Working for a fast paced CRO.
Regulatory Affairs Specialist-Dental Products: TRAINING GIVEN
Hamburg
Aug 28
Looking for a change in your career and the chance to develop into a niche market and become a manager in the future? Look no further!
Regulatory Affairs Associate - Junior Level
South Yorkshire
Aug 28
Regulatory Affairs Associate - Junior Level

Need to gain more experience in order to climb the ladder within the regulatory affairs market? Then apply now for the position as a Global Regulatory Affairs Associate and work for an established company that will give you exactly that opportunity, to grow and build allowing you to obtain new skills.
Senior Regulatory Operations - Client Facing
Middlesex
Aug 28
Regulatory Operations - Consultancy - Home based

I am looking for a Regulatory Operations focused consultant to work with a global CRO working on an exciting new venture for the company.
Regulatory Operations - Consultancy - Home based
Basingstoke
Aug 28
Regulatory Operations - Consultancy - Home based

I am looking for a Regulatory Operations focused consultant to work with a global CRO working on an exciting new venture for the company.
Regulatory Affairs - Successful Career - Galway
Galway
Aug 28
If you are a Regulatory Affairs professional, with 1 or 2 years experience, looking for a next step in your career, this is your chance to join a global company and build a successful professional path.

My client is the largest pharmaceutical company producing generics. They are seeking for an ambitious Regulatory Affairs Specialist, a junior ambitious professional that will lead with EU/Worldwide submissions and approvals of generics.
Regulatory Affairs Project Manager: Publishing Product License and Submission Management
Surrey, UK
Aug 28
This is a new opportunity available immediately suitable for an experienced Project Manager. You’ll join a discreet project involving submissions management for a Blue Chip Pharma organisation. We’re looking for someone well adept at contributing to global projects, and with excellent communication & interpersonal skills. Excellent contract working on the client site in Surrey, UK. 12 month contract in the first instance.
Senior Regulatory Affairs Specialist – Global Medical Devices – Excellent Salary and Benefits Package
England
Aug 28
My client – a Global Medical Device company with an extensive portfolio of products are looking for an experienced regulatory affairs professional to join their established Regulatory team as a Senior Regulatory Affairs Specialist based in the South East
Regulatory Affairs Manager
Maidenhead, Berkshire (some travel)
Aug 28
We are currently looking for strong manager-level regulatory professionals to lead our teams of consultants. People skills are an absolute must; we expect our managers to lead from the front, demonstrating clear communication skills and with a strong focus on people-development. The role requires you to take responsibility for the line management of a team of our permanent members of staff including managing goals and objectives, and training and development
Regulatory Compliance Manager-Niche Area-Medical Devices-CH
Basel
Aug 28
Work within the niche area of regulatory compliance with this fantastic management role with a world leading medical device company. Be the next regulatory affairs compliance and vigilance manager to work on innovative class I through to class III devices. Our client are looking for an experienced regulatory affairs professional within the medical device industry who international expertise. If you are looking for your next role in management, apply now.
Associate Director - Regulatory Affairs Manager - UK or Germany
Germany
Aug 28
Our client is a growing CRO passionate about rare diseases. As a result of a spectacular growth, they are looking for a new member in their team : Associate Director/Regulatory Affairs manager. This is a permanent position, office based in either Frankfurt (Germany) or Guildford (UK). For more information or to apply, please contact Sandrine Falco +44 118 3805615 or email sfalco@planet-pharma.co.uk
Regulatory Project Manager
Maidenhead, Berkshire (some travel)
Aug 28
There has never been a more exciting time to join our team at Genpact Pharmalink. Our Project Managers take responsibility for either single or multiple projects, utilising our team of regulatory experts, various technology platforms and other resources available to them. We are looking for elite candidates who are both consultative in their approach, solutions and goal-orientated as well as being client-focussed and diplomatic.
Regulatory Affairs Associate
Sydney
Aug 28
Join a pharmaceutical leader with a strong commitment to growth and innovation have an exciting opportunity to develop your career in regulatory affairs.
Senior Regulatory Medical Writer
England
Aug 28
I am currently recruiting for one of our biggest and most exciting clients who are looking to add to their vibrant Regulatory team. They are one of the world’s leading pharmaceutical companies and are looking to bring a number of experienced Regulatory Medical Writers to their already rapidly expanding organisation.
Global Regulatory Manager - Broad role - Germany
Frankfurt am Main
Aug 27
An interesting opportunity has just come up to work a very broad and interesting role in regulatory affairs, focusing on the entire DACH region for my client in Germany. ...
Regulatory Affairs Manager Europe
Dublin
Aug 27
My client is one of the leading top ten animal health companies in the world and they are looking for a regulatory affairs manager. The company has a presence in over 100 countries worldwide and has a growth rate of 20% year on year.
Regulatory Submissions Manager
London (Hammersmith) or Stirling, United Kingdom
Aug 27
Medpace is seeking a Regulatory Submissions Manager for our office in London (Hammersmith) or Stirling, United Kingdom.
Regulatory Affairs Manager (100%)
Zürich
Aug 27
Regulatory Affairs Manager, Local Markets, Generics, Excellent Career Options, Zurich Region
Regulatory Affairs Specialist
Slough
Aug 27
My client, a successful international pharma company, is looking for a Regulatory Affairs Specialist to join their Regulatory Affairs department in Berkshire UK.

For this position you will be in charge of the submissions, redaction and registration of documents in UK and Ireland. You will provide regular support to Global Regulatory Affairs (GRA) colleagues in delivering strategic and operational regulatory plans and activities. ...
Associate Director of Regulatory Affairs - UK/IRE – Top Pharma
London
Aug 27
This Associate Director of Regulatory Affairs role is a senior level role where you'll have operational responsibilities for the local UK/IRE office. With the company having just secured new investment you'll be working with a new team who have fresh ideas and motivation, allowing you to really stamp your mark here. You'll also act as the UK/IRE expert on global portfolio matters ensuring you can still have the stimulating Inte
Reg Affairs Assistant-Regulatory Affairs is FUN
Amsterdam
Aug 27
Regulatory Affairs is fun whilst working for this young, dynamic and innovate company in the market of self-care products, a niche area giving you the opportunity to become an SME and broaden your experience and future career options.Based in Amsterdam you will join a self-care OTC company ensuring their Regulatory requirements are met on a daily basis.
Associate Director of Regulatory Affairs – Strategy Lead – UK
London
Aug 27
This is an outstanding opportunity to join a new RA team where you'll be responsible for driving the regulatory strategy in the EMEA and Emerging Market regions. Working in the field of Biologics on a portfolio level this role will offer you centralised project management without the stresses and strains of line management. With a rare disease focus this role also offers you a highly rewarding product portfolio.
Global Regulatory Associate - Diversity
South Yorkshire
Aug 27
Global Regulatory Associate - Diversity

Apply now and work as a Global Regulatory Affairs Associate in a diverse environment which will give you the opportunity to learn from others who have obtained experience on a global level. Take this opportunity to not only meet new people from other backgrounds but to also boost your profile and pick-up new global skills.
Regulatory Affairs Manager
Berkshire
Aug 27
Regulatory Affairs Opportunities:

We have had a lot of demand for talented Regulatory Affairs professionals from Regulatory Managers / Team Leaders down to Regulatory Associates over the past few weeks. If you are keen to apply or learn more information about the roles below please get in contact with our Senior Regulatory Consultant Natalie Hopkins by emailing your C.V for an informal discussion on relevant opportunities in the market. Send your details to n.hopkins(a)realstaffing. ...
Regulatory Business Analyst
Kent
Aug 27
Regulatory Business Analyst

Summary - 12 month rolling contract with leading Pharma company. Get a working knowledge of the business goals of a multinational company.

Analyst...
Senior Regulatory Executive
Middlesex
Aug 27
Our Global Pharmaceutical Client are looking for Senior Regulatory Executive to join their team for 9 months in Middlesex.
Global Regulatory Affairs Manager - Hessen - Germany
Frankfurt am Main
Aug 27
A very interesting opportunity has just come up to work within global regulatory affairs for large well respected clients in Germany. The positions currently available are for global regulatory affairs managers for Germany, respectively for the whole DACH region. Performing these positions will provide the experience necessary to manage any regulatory department on a global scale and will also greatly enhance your experience in liaising with regulatory agencies for the DACH region. ...
Regulatory Affairs Specialist - International Company - Galway
Galway
Aug 27
I am seeking for a young professional in Regulatory Affairs with at least 1 year experience in the pharmaceutical sector. This is your opportunity to take an important next step in your life joining an International Company that will allow you to build a successful career.

My client, the largest pharmaceutical company producing generics, is looking for an ambitious Regulatory Affairs Specialist, that will lead with EU/Worldwide submissions and approvals of generics.
Regulatory Intelligence Manager
London
Aug 27
Regulatory Intelligence Manager

Summary - 12 month rolling contract with leading multinational Pharma company in Greater London

Manager Responsibilities

-provide expertise on regional regulatory requirements in emerging markets...
Regulatory Affairs Project Manager
Kent
Aug 27
Regulatory Project Manager
Full Time, Permanent
South East, UK
Attractive Salary and Benefits package.

SSU and Regulatory Specialist II - Poland
Poland - Any INC Office
Aug 27
INC Research employees don't accept ordinary. From therapeutic experts to administrative support staff, each member of our 5,000-strong team continually searches for better. Whether that's better clinical development through our unique Trusted Process®, or better insights from the 100-plus countries in which we operate. It means we deliver success faster, not only for our customers and the patients we serve, but also ourselves.
Senior Regulatory Affairs Manager - CMC Strategy (m/w)
Basel
Aug 27
Senior Regulatory Affairs Manager – CMC Strategy (m/w)
Office-based in Basel


Job Description:

You are responsible for developing global technical regulatory strategies in support of all the development and marketed products within the portfolio. By working with technical product teams, the department is responsible for assuring that quality regulatory submissions are generated and comply with the highest Health Authorities standards world-wide. ...
Regulatory Affairs Specialist Medical Devices
Solothurn
Aug 27
My client is an established American Medical Device company currently expanding and looking for a Regulatory Affairs Specialist to join them in their Swiss office based near Lausanne and Geneva region.
SSU and Regulatory Specialist II - UK
UK - Any INC Research office
Aug 27
INC Research employees don’t accept ordinary. From therapeutic experts to administrative support staff, each member of our 5,000-strong team continually searches for better. Whether that’s better clinical development through our unique Trusted Process®, or better insights from the 100-plus countries in which we operate. It means we deliver success faster, not only for our customers and the patients we serve, but also ourselves.
Regulatory Affairs Manager - CMC Biotech (m/w)
Basel
Aug 27
Regulatory Affairs Manager – CMC Biotechnology (m/w)
Office-based in Basel


Job Description:

As a Drug Regulatory Affairs Manager CMC in the Biotech Development Group, you set and maintain the technical regulatory standards for the Chemistry Manufacturing and Control (CMC) submissions. You will be responsible for providing strategic advice and proactive regulatory input to the internal functions for the management of products under development. ...
Senior Regulatory Affairs Manager-Medical Devices
Mannheim
Aug 27
My client is an established start-up Medical Device company with products on the world market leader in ophthalmology. Due to growth my client is looking for a Regulatory Affairs Manager to join their German office near Mannheim.
Regulatory Affairs Manager, Broad Responsibilities, Zurich
Zürich
Aug 26
Regulatory Affairs Manager, Broad Responsibilities, SwissMedic Lead, Growing Team
Regulatory Submissions Manager - Munich, Germany – Top 20 CRO – Up to €75,000 basic salary and no travel
Germany
Aug 26
English, German, Munich, Munchen, Germany, Study Start-Up Specialist, SSS, ethics submissions, contract negotiation, phase I-IV, clinical trials, CRO, English Study Start-Up Specialist, SSS, ethics submissions, contract negotiation, phase I-IV,
REGULATORY AFFAIRS SENIOR DIRECTOR, BIOLOGICS, BELGIUM (HOME BASED)
Belgium, Brussels, Home Based
Aug 26
A great new opportunity has become available for a biologics expert at a leading CRO. This position can be home based anywhere in the EU including Belgium.
Regulatory Affairs Specialist
Office Based
Aug 26
I am working with a growing pharmaceutical company for are looking for a regulatory Affairs Specialist to join their UK team also working with the German Office with occasional travel.
Senior Regulatory Affairs Specialist
Office Based
Aug 26
Calling all Senior Specialist Regulatory Affairs professional ....
Study Start Up Manager/Regulatory Start Up Manager – Emerging mid-size CRO - USA
Office based – multiple US locations
Aug 26
Study Start-Up Manager/Regulatory Start Up Manager: This is an exciting opportunity for you to join a fast-growing top 20 CRO in a leading role within their Regulatory and Start Up team. There is plenty of scope for strong career progression as you aid this organisation with their growth and development. Ideal for someone with experience in Project Management and Study Start Up looking to go to a slightly smaller CRO.
Regulatory Affairs Specialist-Growing Team-Devices-Switzerland
Zürich
Aug 26
Join a growing regulatory affairs team today! Apply now for this regulatory affairs specialist role which will give you the opportunity to join an international medical device company at their exciting point of growth. Our client are looking for an experienced regulatory affairs professional from the medical device industry. Interviews are already being set up for this role, so ensure you apply now to find out more.
Regulatory CMC Advisor
Switzerland
Aug 26
Our client is currently expanding their team and looking for CMC experts to join them. With an impressive product portfolio this organisation strives to attract high quality staff and is renowned for being one of the best employers in their division. You will be responsible for independently providing strategic and operational global CMC regulatory whilst coordinating change controls and facilitating the timely writing of CMC modules.


Global Regulatory Director in Ophthalmology – Switzerland
Switzerland
Aug 26
An opportunity to join one of the world's largest pharmaceutical companies based in their Headquarters in Switzerland. With an impressive product portfolio and strong pipeline, our client is looking for a highly experienced Regulatory Professional to join them within their Ophtalmology franchise.

You will be responsible for defining and implementing the global regulatory strategy for the development, submission, approval and life cycle management of your designat
Regulatory Affairs Specialist: Technical Writing-Devices-Berlin
Berlin
Aug 26
My client a growing international medical devices company, is look for a Regulatory Affairs Technical Specialist to join their department in Berlin...
Global Head of Regulatory Affairs Labeling
Switzerland
Aug 26
My client, one of the world's leading Pharmaceutical companies is looking for a strategic and capable Global Head to them. In this senior role you will be leading a team of Therapeutic Areas Leads in the Global Labeling Group for the development and review of Labeling. You will lead Product Information Policy and be responsible for the development and implementation of adequate processes to ensure adherence to this policy.
Regulatory Vigilance Manager-Cross Function Role-Devices-CH
Basel
Aug 26
Gain the fantastic opportunity to be the next regulatory vigilance and compliance manager with a world leading medical device company based in the Basel region. Our client are looking for an experienced regulatory affairs professional from the medical device industry, with expertise in both compliance and vigilance. This is a great management role to specialise in a niche area within regulatory affairs develop invaluable expertise.
Regulatory Affairs Manager – International – Österreich
Austria
Aug 26
Als Regulatory Affairs Manager sind Sie an der strategischen Ausrichtung der Abteilung beteiligt. So schauen Sie, wie man den Zulassungsprozess vereinfachen und effizienter gestallten kann. Weiterhin arbeiten Sie an der Erstellung von Zulassungsdokumenten mit Fokus auf CMC Dokumentationen. Weiterhin stehen Sie in Kontakt mit den verschiedenen Zulassungsbehörden, beantworten deren Fragen und implementieren neue Richtlinien.
Regulatory Affairs Director - IVD - Bavaria
Bavaria
Aug 26
My client in the Bavaria Region is offering a fantastic opportunity for professionals to join the Regulatory Affairs Department. This opportunity is rare to come by as the client is looking for motivated individuals who are looking for a long term career with this company and what they are willing to offer in return is EXCELLENT...
Regulatory affairs CONTRACT ROLE – Brussels – International strategy for Global submissions – To 80 Euros per hour
Brussels, Belgium
Aug 26
This organisation has been voted one of the best companies to work for in Belgium and are based in Brussels (with excellent transport links). 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 Andrew Barnes our Swiss office, on +41 41 710 5100
Regulatory Affairs - Contracts
Cambridgeshire
Aug 26
Regulatory Affairs - Contracts

We specialise within the Regulatory Affairs Market and understand what our candidates and clients are looking for. We are not a generalist recruitment agency having developed over 15 years of experience within this industry, which gives us the competitive edge to providing you with opportunities that fit with your skill set.
Regulatory Associate - Life-cycle
South Yorkshire
Aug 26
Regulatory Associate - Life-cycle

Take this fantastic opportunity to broaden your global regulatory affairs experience across the entire life-cycle which will in essence broaden your skill set making you more attractive to future employers, increasing your chances of more job opportunities.
Senior/Regulatory Affairs Officer
Midlothian
Aug 26
Oliver Care is recruiting for a Senior/Regulatory Affairs Officer to join a company in the Medical Device industry at their site based in Midlothian on...
REGULATORY AFFAIRS, ASSOCIATE MANAGER MDandD - PERM
Stevenage, Herts
Aug 26
Regulatory Affairs, Associate Manager required by Novella Clinical. Strong Medical Devices experience required. Office based in Hertfordshire, UK.
Regulatory Compliance Administrator
South West London
Aug 26
Our client is looking for a Regulatory Compliance Administrator to be based in South West London. The company is involved in Phase I-IV research trials including pharmacokinetic studies in patients, and healthy volunteer studies.
Regulatory Affairs Manager - Medical Devices
Switzerland
Aug 26
Regulatory Affairs Manager - Medical Devices
Senior Regulatory Affairs Manager, Regulatory Intelligence
Uxbridge
Aug 26
Our client is a leading Biotech who currently have a 12 month contract for a Senior Regulatory Affairs Manager within Regulatory Intelligence.

As the successful candidate you will facilitate product registration by providing the right information to the right people at the right time. ...
Senior/Regulatory Affairs Officer
West Lothian
Aug 26
Are you an experienced Regulatory Affairs Officer looking for an exciting new position within a global company?
Regulatory Affairs Director - CMC
Switzerland
Aug 26
A leading global pharmaceutical company with a diverse healthcare portfolio and their products sold in more than 150 countries around the world are looking for a professional and experienced individual to fill their Regulatory Affairs Director- CMC position, based in their headquarters in Switzerland.
PW 6091 Regulatory Affairs Manager, Europe
West London
Aug 26
This excellent contract opportunity will support early phase research & development programmes across Europe, regulatory submissions to the European Medicines Agency (EMA) and post-authorisation activities.
Quality and Regulatory Manager (Medical Devices)
North West
Aug 25
A growing aesthetic dermatology portfolio due to recent acquisitions has created a senior position within the company’s Technical Team. You will be an effective project leader with 5-8y in the Regulatory & Quality area (medical devices) to include experience with US FDA submissions of new products and implementing lean manufacturing principles. With a Corporate HQ in London, an Operations HQ in Paris and contract manufacture in the US there are frequent opportunities for international travel
Regulatory Affairs Manager - CIS (m/w)
Köln
Aug 25
Regulatory Affairs Manager (m/w)
Office-based near Cologne


Job Description:

? Ensure that all product documentation (CMC and formal pharmaceutical assessment) is compliant with current industry regulations
? Develop suitable regulatory strategies for all products.
? Managing successful initiation, execution and completion of Regulatory and CMC projects. ...
jobs : 100 +
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