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The latest Regulatory jobs - BETA

Jobs: (Regulatory)

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Regulatory Affairs Manager, Development Products
Basel
Jan 23
Regulatory Affairs Manager/Senior , development products, global HQ, EMA, strategic and hands on focus. Salary package competitive with Big Pharma, relocation help is available
Regulatory Affairs Manager, CMC, Austria
Salzburg
Jan 23
Regulatory Affairs Manager, CMC, technical and strategic input, global pharmaceutical company working on products in development and established brands
Regulatory and Start-Up Specialist 2 (f/m) - based in Uppsala
Uppsala
Jan 23
This is a crucial role within QuintilesIMS and the opportunity to start or progress your career in clinical research. It is a position, which offers development options for an experienced Start-Up Specialist or a CRA who is looking for a new challenge. You will manage start up activities for clinical trials in accordance with applicable local and/or international regulations, our companies’ standard operating procedures, project requirements and contractual guidelines. ...
Regulatory and Start-Up Specialist 1 or 2 (f/m) - office based in Espoo
Espoo
Jan 23
This is a crucial role within QuintilesIMS and the opportunity to start or progress your career in clinical research. With this position, we are offering a variety of development options for an experienced Start-Up Specialist, a CRA who is looking for a new challenge or a graduate of a life science related field. ...
Regulatory Affairs Officer– Team work– Brussels
Brussels
Jan 23
A big pharmaceutical company is looking for a Regulatory Affairs Officer because there Benelux regulatory team needs support. You will work together with the team on the Vaccines portfolio where you can gain more experience for these promising products. In that way you can divide the tasks and learn from each other.
Specialist or Senior Specialist - Global Regulatory Affairs - Ukraine
Ukraine,homebased
Jan 23
Worldwide Clinical Trials (WCT) currently have a new vacancy to support activities due to new projects. Experience in Global submission is required. Company: Worldwide Clinical Trials Ltd Location: Home based Ukraine Reference: Type: Permanent Salary (£): On Application (Highly competitive) Benefits: Bonus + benefits
Regulatory Affairs Global CMC Director - Cover EU, US, Japan, Emg and LatAm – Based in Brussels - Great Salary, Bonus, Car and LTI Package
Brussels
Jan 23
Work on Global CMC projects - Have real autonomy, scope and responsibility for your own varied product portfolio - Lead a strong global team of regulatory CMC experts/professionals. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380
Regulatory Lead Paediatrics – global pharma company – Frankfurt – up to 130,000 € - all applicants within EU welcome
Germany
Jan 23
We are looking for an experienced Regulatory Affairs Manager, who wants to use his knowledge about pediatric development in one of the biggest pharmaceutical organizations worldwide. You can expect an open environment, life-changing projects and excellent benefits.
Regulatory Affairs Director, Europe – Full project lifecycle role covering Development and EU MAA’s
Utrecht, Amsterdam, Leiden, Rotterdam, Amersfoort
Jan 23
This is a hands-on role where you will have leadership of your projects, as you report into a highly engaging and experienced Head of Regulatory Affairs. As the company grows so will this role as there are strong expansion plans already in place. To apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion a call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
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REACH Worldwide Notifications - Regulatory Manager
Amersfoort
Jan 23
This a senior position where initially you will be working on REACH registrations with the eye on the 2018 deadline. Being hands-on responsible to build dossiers and verifying risk assessments. At the same time you will have the chance to expand your skill-set and get experience with IFRA notifications and cosmetics registrations. Also after 2018 you will have job stability, with Worldwide Notifications for REACH, compliance, and continuous cosmetics regulatory work.
New Regulatory Affairs Director Role - Global MAA strategy and Team Leading – Great Salary and Package
Brussels
Jan 23
Responsible for the development and implementation of regional regulatory strategies aligned globally for assigned products - • Working with the US/EMEA regional team lead to drive consistency and global working across both teams. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Director for Immunology - Lead Strategy and Development and EU MAA’s + Lead a strong team of regulatory performers
Brussels
Jan 23
Operate as the Regulatory lead for a Global Brand in Immunology - Lead the development and Implementations of regulatory strategies for MAA’s within the EMEA region - Identify future commercialisation opportunities for worldwide markets - Manage strong team of regulatory performers. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Director EMEA Team Leader Manage EMEA regulatory submissions for an expanding Biotech
Brussels
Jan 23
You will manage a strong regulatory team of managers and senior managers proving input on regulatory strategy within EMEA region, all for a company with excellent sales and 1st class resources in a role which will be varied & broad-based. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
ASSOCIATE DIRECTOR, EUROPEAN REGULATORY AFFAIRS, MARKET PRODUCTS - Office based London or Home based
Office based London or Home based
Jan 23
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 Health Sciences as an Associate Director, European Regulatory Affairs, Marketed Products and help realize your career potential.
Regulatory Submissions Manager
England
Jan 23
Regulatory Submissions Manager - Home-basedMy client, a leading Regulatory Affairs CRO, is looking for an experienced CTA candidate to join their development team as a CTA Submissions Manager. My client works with over 400 global pharmaceutical and biotechnology customers and they need a strong candidate to work co-ordinate and lead CTA Submissions. Candidates must be eligible to work in the UK. ...
Home Based – Regulatory Writer – Global CRO – 12 Month Contract
England
Jan 23
This world leading CRO is after experienced medical writers who can come in on a contract basis and hit the ground running. This position is 100% home based allowing you to work on a range of global projects.
Regulatory Affairs Consultant-German Speaking
Germany
Jan 22
Regulatory Affairs Consultant- 6 Month contract- Immediate Start- Germany, German Speaking Level: Regulatory Affairs Consultant Contract: 6 Months Location: Germany, EU Language: German and English Summary We are urgently looking for a Regulatory Affairs Consultant to management activity for Germany. The successful candidate will be German speaking complete local submissions of marketing authorization applications for a diverse pharmaceutical portfolio. ...
Head Regulatory Affairs–Big Player-Belgium
Belgium
Jan 22
A pharmaceutical company is looking for a Head Regulatory Affairs to lead the Benelux department. The company is a well-established multinational and you will be responsible for the Consumer Health portfolio. The company has also other divisions with different product lines which gives them a higher market value and better future financial stability. It is a great chance for you to get more internal opportunities (horizontal and vertical growth) and add value to your CV.
Senior Regulatory Affairs Manager in Spain
Barcelona
Jan 20
I am currently recruiting for a Senior Regulatory Affairs Manager for a small set up based near Spain. This would be a varied and hands on position will allow you to take more responsibility whilst also receiving first class guidance and training.
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Regulatory Affairs Specialist-Manager (Medical Devices) / global, international Company
France
Jan 20
A unique Regulatory Affairs Manager job for an organised Regulatory Manager in a global operating company for Medical Devices in Classes 1 – 3. This...
Regulatory Affairs Specialist-Manager (Medical Devices) / global, international Company
Poland
Jan 20
A unique Regulatory Affairs Manager job for an organised Regulatory Manager in a global operating company for Medical Devices in Classes 1 – 3. This...
Regulatory Affairs Specialist-Manager (Medical Devices) / global, international Company
Spain
Jan 20
A unique Regulatory Affairs Manager job for an organised Regulatory Manager in a global operating company for Medical Devices in Classes 1 – 3. This...
Senior Regulatory Affairs Associate Medical Device - global healthcare company - Belgium - 50,000 €
Belgium
Jan 20
We are looking for a Senior Regulatory Associate, who likes to work in a global and diverse company and will take credit for operational tasks within a medical device team. You can expect to work in a small but already good developed medical device team with a great environment and exciting product portfolio.
Regulatory Affairs Manager, Geneva, (80-100%)
Genève
Jan 20
Regulatory Affairs Manager, Geneva, Broad Coverage for QA/PV/RA, Growing Affiliate
Senior Associate, Regulatory Affairs
England
Jan 20
A superb opportunity has arisen for an ambitious and industrious individual to work on multiple varied projects utilising and acquiring numerous skills. You will be working with a well-established and growing CRO within a team with an increased focus on key projects working with key clients. They do have multiple sites worldwide and they are currently looking to expand their team in the UK.
EU Regulatory Affairs Manager, Basel, CP/DCP
Basel
Jan 20
EU Regulatory Affairs Manager, Basel, CP/DCP
Senior Regulatory Affairs Associate, Medical Devices (Scotland) - NCR
Homebased
Jan 20
Regulatory Affairs, Medical Devices, MD&D, Regs RA
Regulatory Operations Project Manager: Frankfurt
Germany
Jan 20
Regulatory Operations Project Manager Frankfurt Salary: Up to €75,000 (DOE) plus package I am now working with a leading Pharmaceutical business in Frankfurt to recruit an experienced Regulatory Operations Project Manager to work on some ground breaking projects within the business.
Regulatory Affairs Manager
Vaud Area, Switzerland and Barcelona Area, Spain
Jan 20
Edelway is a pan-European Pharma Consultancy. One of our best clients, a global, pharmaceutical company based in Vaud Area, Switzerland and Barcelona Area, Spain is currently looking for experienced Regulatory Affairs Manager.
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Head of Regulatory Affairs
Kirklees
Jan 20
My Client and I are looking to speak to individuals who have the required skills to fit a great opportunity as the Head of Regulatory Affairs within one most established players.
Regulatory Affairs Associate, Medical Devices (Scotland) - NCR
Scotland
Jan 20
Regulatory Affairs, Medical Devices, Scotland, Glasgow area
Senior Regulatory Affairs Manager
Switzerland
Jan 20
Senior Regulatory Affairs Manager - Development function - International role
Regulatory Affairs Officer – North Wes
North West England
Jan 20
I am currently working with a generics company base in the North West of England who are searching for a new Regulatory Affairs Officer. This company have an excellent product pipeline coming through and are expecting this position to grow in seniority over the course of the next few years.
Regulatory Labelling Manager (m/f)
Baar
Jan 20
Regulatory Labelling Manager (m/f) in Baar Our clients is an internationally leading Medical Technology Company who offers an exciting tailored career path for your professional and personal development within their Regulatory Affairs & Quality Assurance team. The client is specialized on heart diagnosis, monitoring as well as software solutions. The manufacturing takes place in Switzerland and the products are distributed worldwide. ...
Regulatory Affairs Manager GI
South East England
Jan 20
An opportunity to work within a unique global pharmaceutical company who are focused on developing and manufacturing both branded, OTC and innovative and branded pharmaceuticals
Regulatory Affairs Manager and Lead Client Services
Ingelheim am Rhein (55218)
Jan 20
Our client is a market leading management consultancy. Their Life Sciences Vertical focuses on providing services to support customers to run their existing business better and to develop their business model further to succeed in the drug development and clinical trials phases.To support a client site in Germany, they need experience in Clinical Regulatory Affairs while having impecible communication skills. ...
Manager, Regulatory Affairs (Functional Initiatives)
USA
Jan 20
My client is a recently formed, global, research-based bio-pharmaceutical company. The company's mission is to use its expertise and unique approach to innovation to develop and market advanced therapies that address some of the world's most complex and serious diseases. They operate in over 170 countries.
Associate Director, Regulatory Affairs - Global Regulatory Strategy (Oncology)
USA
Jan 20
My client is a recently formed, global, research-based bio pharmaceutical company. The company's mission is to use its expertise and unique approach to innovation to develop and market advanced therapies that address some of the world's most complex and serious diseases. They operate in over 170 countries.
Regulatory Manager (m/f)
Aachen,Germany
Jan 20
For an independent, family-owned, international research-based pharmaceutical company DOCS is looking for an experienced Regulatory Affairs Specialist (m/f) on interim basis for 12 months to support international regulatory projects, preparing and implementing regulatory plans and managing regulatory submissions.
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Regulatory Affairs Specialist-Manager (Medical Devices) / global, international Company
Lisbon
Jan 19
A unique Regulatory Affairs Manager job for an organised Regulatory Manager in a global operating company for Medical Devices in Classes 1 – 3. This...
Regulatory Affairs Manager (medizinsche Geräte) / Norddeutsches- Traditionsunternehmen
Germany
Jan 19
Eine einmalige Chance als Regulatory Affairs Manager im Bereich medizinische Geräte und Produktzulassung der Klasse 1 -3, Teil eines globalen, internationalen Unternehmens zu werden. In...
Senior Regulatory and Site Services Specialist - office based in Leuven
Belgium
Jan 19
Our successful and dynamic team in Belgium is currently looking to expand. Are you searching for an exciting new role? Do you have any experience in start-up and regulatory affairs? Then this is a fantastic opportunity for you! We are looking to recruit a Senior Regulatory and Site Services Specialist - office based in Leuven
Senior Manager and Regulatory Strategy
England
Jan 19
Genpact Pharmlink is a highly specialised Regulatory Affairs Consultancy with a successful history. The success of Genpact Pharmalink depends on its people. Capitalizing on what is unique about individuals and drawing on their different perspectives and experiences will add value to the way we do business.
Senior Manager and Regulatory Strategy Lead, Cambridge
England
Jan 19
Genpact Pharmlink is a highly specialised Regulatory Affairs Consultancy with a successful history. The success of Genpact Pharmalink depends on its people. Capitalizing on what is unique about individuals and drawing on their different perspectives and experiences will add value to the way we do business.
Regulatory Affairs Specialist-Market Leader-Munich, Germany
München (81249)
Jan 19
NonStop Medical Devices are currently looking for a regulatory affairs specialist to join our client, a market leading medical device company.
Post Regulatory- Belgium-
Brussels
Jan 19
Amazing opportunity to get into the Medical Device Industry for junior Post Regulatory Professionals
Work in Prague- Regulatory-
Prague
Jan 19
Looking urgently for Regulatory Professionals keen to work in Prague
Associate Director/Director - Regulatory Affairs
USA
Jan 19
My client is a leading science-based bio-pharmaceutical company that discovers, invents, develops, manufactures, and commercialises medicines for the treatment of serious medical conditions.
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Regulatory Affairs Manager - Promotional Material and Regulatory Excellence
London
Jan 19
For more information on this job or others please get in contact with our Senior Consultant Sam Murphy on 0208 544 3423 / 07971 477 589 sam.murphy@tecgroup.net
Senior Regulatory Associate / Associate Regulatory Manager
England
Jan 19
For more information please contact Sam Murphy via email sam.murphy@tecgroup.net / 0208 544 3423
Regulatory CMC Manager
Cambridge or London
Jan 19
For more information or to apply to this position please contact Sam Murphy – Senior Consultant at the TEC Group International via +44 (0)208 544 2324 / sam.murphy@tecgroup.net
Senior Associate Regulatory Affairs / Junior Manager of Regulatory affairs
Germany
Jan 19
The consultant running this executive search is Sam Murphy. For more information or to apply to the position please contact Sam via email – sam.murphy@tecgroup.net
International Regulatory Projects Manager
England
Jan 19
For more information on this or other positions please contact Sam Murphy - sam.murphy@tecgroup.net / 0208 544 3423
Senior Vice President of Global Regulatory Affairs
England
Jan 19
This position is retained by Sam Murphy of TEC Group. For more information on this position or any other global regulatory position please speak to Sam Murphy our Senior Consultant for Global Regulatory Affairs. 0044 (0) 208 544 34 23 / sam.murphy@tecgroup.net
REGULATORY AFFAIRS OFFICER
UK
Jan 19
Working as part of a young and dynamic team of regulatory experts. This position is perfect for a forward-thinking regulatory Associate. My client are seeking a very motivated regulatory officer for the Belgium office to help keep the company at the top of the industry. This position will allow the candidate to have a creative platform to grow and learn within the company.
Senior Regulatory Affairs Manager Belgium
Belgium
Jan 19
For more information or to apply for the position please contact Sam Murphy at the TEC Group International. 0208 544 3224 / sam.murphy@tecgroup.net
Senior Regulatory Associate
London or Manchester
Jan 19
If you feel as though your skills and experience are in line with the expectations we would be keen to hear from you. Please get in contact with the Senior Regulatory Affairs consultant at TEC Group International Sam Murphy 02085443423 / sam.murphy@tecgroup.net TEC Group International have been appointed by Omega Pharma/Perrigo as the exclusive recruitment partner for this campaign and all enquiries should be directed through TEC Group.
Regulatory Senior Associate - London or Midlands
England
Jan 19
If you feel as though your skills, experience and personality can bring value to this business, we would be keen to hear from you. Please get in contact with the Regulatory Affairs consultant at TEC Group International Sam Murphy 02085443423 / sam.murphy@tecgroup.net TEC Group International have been appointed by Omega Pharma/Perrigo as the exclusive recruitment partner for this campaign and all enquiries should be directed to TEC Group.
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Regulatory Biological CMC Specialist (ATMP) England Relocation.
Rep. Ireland
Jan 19
For more information or to apply to this position please contact Sam Murphy – Senior Consultant at the TEC Group International via +44 (0)208 544 2324 / sam.murphy@tecgroup.net
Clinical Trial Regulatory Senior Manager UK
England
Jan 19
To apply for this position please contact Sam Murphy Senior Consultant at the TEC Group international - 0208 544 23 24 / sam.murphy@tecgroup.net TEC Group International offers a referral reward for this particular positions. If you refer a candidate that completes the hiring process successfully we will reward you £500!
Executive Director of Regulatory Affairs.
England
Jan 19
The consultant running this executive search is Sam Murphy. For more information or to apply to the position please contact Sam via email – sam.murphy@tecgroup.net
Senior Regulatory Manager (Lausanne)
Lausanne
Jan 19
My client is a specialty pharmaceutical company with a focus on development of novel drug candidates. Working in partnership with medium to large pharma they have an enviable record of developing drugs which have high value impact for patients worldwide. They are looking for a Senior Regulatory Affairs Manager to join their team in Lausanne, Switzerland. ...
Senior Regulatory Affairs Manager
Harlow
Jan 19
Are you keen to join a leading regulatory affairs team? Do you have regulatory experience with branded products? We're looking for someone like you… Teva currently have an excellent opportunity for a Senior Regulatory Affairs Manager to join the branded Regulatory team, focusing on Pain as a therapeutic area.
Regulatory Consultant - Agchem - Work from home
Derby
Jan 19
Regulatory Consultant - Agrochemicals - Work from home or from the UK or Swiss OfficesOur client is offering multiple vacancies within Biocides or Agrochemicals in a position allowing you to maximise a flexible working approach whilst taking on exciting projects - multiple projects at a time. The scope of work will centre mainly around Plant Protection / PPP but can take into consideration other regulatory projects such as agrochemicals. ...
Regulatory Consultant - Biocides - Work from home
Derby
Jan 19
Regulatory Consultant - Biocides - Work from home or from the UK or Swiss OfficesThis is an excellent opportunity to take on a position allowing you to maximise a flexible working approach whilst taking on exciting projects - multiple projects at time. The scope of work will centre mainly around biocides but can take into consideration other regulatory projects such as agrochemicals. ...
France Regulatory Lead and Responsible Pharmacist - Paris
Paris
Jan 18
France Regulatory Lead & Responsible Pharmacist My Client is a growing pharmaceutical company is looking for a France Regulatory Lead & Responsible Pharmacist to join their Research & Development team on a permanent or contract basis. This is a great opportunity for an experienced professional to be part of all regulatory aspects from product conception to market release. ...
Regulatory Affairs - Long-Term Development - CTD-Dossiers
Rheinland-Pfalz
Jan 18
Regulatory Affairs - Long-Term Development - CTD-DossiersNonStop are working with a long-established German pharma leader, regularly rated as a top employer in the industry. They are looking for an addition to their experienced Regulatory Affairs team in Rheinland-Pfalz, who can develop with the company over the long term.The role itself will involve CTD-Dossiers, Regulatory Project Management, and offers control of affairs across the company’s broad and successful portfolio. ...
Regulatory Affairs Specialist (medizinsche Geräte) / junges Unternehmen / Karrieremöglichkeiten
Germany
Jan 18
Eine einmalige Chance als Ingenieur und Regulatory Affairs Specialist im Bereich medizinische Geräte der Klassifizierungen 3, Teil eines global operierenden Unternehmen zu werden. Im süddeutschen...
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Expert Regulatory Specialist
Berlin
Jan 18
EPM Scientific are currently looking for an Expert Regulatory specialist to join a diverse and rapidly growing Medtech company who specialize in in-vitro diagnostics. The...
Regulatory Information Management Systems (RIMS) Manager
Wiltshire
Jan 18
Regulatory Information Management Systems (RIMS) Manager Location: Wiltshire Salary: Up to £60,000 per annum + company benefits •Have over 15 years sector expertise and still rapidly growing.
Regulatory Affairs Team Leader
England
Jan 18
This is an excellent opportunity for a regulatory professional to join an international Bipharma within their regulatory department. You will be responsible for developing and managing a small team of regulatory professional focusing on the development and registration of allergy medicines.
Regulatory Affairs Consultant
Dublin
Jan 18
On behalf of our client, a Dublin based regulatory consultancy firm, we are recruiting for a Regulatory Affairs Consultant.
Regulatory Affairs Specialist-Learn New Skills-Medical Devices
Zürich
Jan 18
Exclusive role within regulatory affairs to develop your career within the niche and exciting area of packaging, labelling and documentation for innovative medical devices. You will work closely with a key regulatory affairs management team of a world leading medical device company and gain exposure to exciting international projects and develop your skills in a niche and lucrative area.
Regulatory Affairs Manager (medizinsche Geräte) / globales Unternehmen
Germany
Jan 18
Eine einmalige Chance als Regulatory Affairs Manager im Bereich medizinische Geräte und Produktzulassung der Klasse 1 -3, Teil eines globalen, internationalen Unternehmens zu werden. In...
Associate Director, Regulatory Affairs
London
Jan 18
A superb new opportunity has arisen with a global market leading Pharmaceutical company. They are currently searching for an Associate Director Regulatory Affairs to join their team in the UK. This is a novel position within the organisation which will allow for further growth of the Regulatory Affairs team.
Regulatory CMC Manager
Tyrol
Jan 18
An exciting new opportunity has arisen with one of our leading Biopharmaceutical clients. We are currently searching for a Regulatory CMC Manager, Biopharmaceuticals. Within this position you will be responsible for the compilation of CMC sections of regulatory dossiers for submissions globally. You would be responsible for writing CMC documentation for marketed products and throughout the development of biopharmaceutical products.
Regulatory Affairs Manager
Tyrol
Jan 18
An exciting new opportunity has arisen with one of our leading Biopharmaceutical clients. We are currently searching for a Regulatory Affairs Manager, Biopharmaceuticals. Within this position you will be responsible for the preparation of regulatory documentation for regulatory submissions globally. You would be responsible for the interaction with Regulatory, Health and Competent Authorities globally and support the development of biopharmaceutical products with regulatory input.
Senior Regulatory Specialist - Medical Devices
Germany
Jan 18
Skills Alliance have partnered with a global Medical Device company to source for a Senior Regulatory Specialist for a position based in Southern Germany. Our...
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France Regulatory Lead and Responsible Pharmacist
Paris
Jan 18
Situé dans Paris intra-muros, un laboratoire novateur cherche un Pharmacien Responsable pour diriger son département des Affaires Réglementaires France. Dans cette petite structure au succès prometteur, vous disposerez d'une autonomie importante dans vos projets et dans le management de votre équipe.
Toxicologist - Risk Assessment and Regulatory
Amersfoort
Jan 18
I'm currently working for a global player for the fragrance and flavours industry. The company has been through a rapid growth phase over the last couple of years and is looking to continue this expansion. To support their growth they are looking for an experienced Toxicologist to join the team.
Regulatory Affairs Assistant
Leeds
Jan 18
Regulatory Affairs Assistant Location: Leeds, UK. Contract: 12 months Regulatory Professionals are currently working with a leading pharmaceutical company and are looking for a Regulatory Affairs Assistant on a contract basis.
Regulatory Affairs Officer– Successful Future– Brussels
Brussels
Jan 18
A big pharmaceutical company is looking for a Regulatory Affairs Officer because there Benelux regulatory team needs support. The company has a diverse product portfolio such as vaccines, pharmaceuticals, consumer health,... Because they have spread their successes in different areas you can be more certain about the stability of your job.
Clinical Regulatory Lead - Luzern
Luzern, Switzerland
Jan 18
This position is for a Senior Clinical Research Associate (SCRA) who excels in regulatory issues and has strong submission experience. You will be outsourced to one designated pharmaceutical sponsor.
Regulatory CMC Associate Manager
Basel
Jan 18
Reg CMC Associate Manager wanted for our Basel based client in the pharmaceutical sector. ...
Regulatory Affairs Manager (Medizinprodukte) / junges Unternehmen / Karrieremöglichkeiten
Germany
Jan 17
Eine einmalige Chance als Ingenieur und Regulatory Affairs Specialist im Bereich Medizinprodukte der Klassifizierungen 3 Teil eines global operierenden Unternehmen zu werden. Im süddeutschen Standort...
Near beautiful Canal City GHENT - Regulatory Manager - Medical Devices - NPD , Strategy and Compliance - International role
Belgium
Jan 17
To apply for this role please call Julie Cooper on 07951 082482 or alternatively send your CV in the strictest confidence to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - near historic Ghent and close to the sea - Manage a team of three -NPD , Compliance , Strategy work
Belgium
Jan 17
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to: Julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager -near to the beautiful canal city of Ghent - Manage a team of three - International role - Medical Devices
Belgium
Jan 17
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to: Julie@mosaicrecruitment.co.uk
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Regulatory Electronic Submission Planner
Kent
Jan 17
Good communication skills, written and verbal, and experience with Microsoft Word and Microsoft Excel. Experience and proven track record in regulatory affairs submissions (In NCE’s and or generics).
Regulatory Electronic Submission Planner
Kent
Jan 17
Good communication skills, written and verbal, and experience with Microsoft Word and Microsoft Excel. Experience and proven track record in regulatory affairs submissions (In NCE’s and or generics).
Associate Director, International Regulatory Strategy
Switzerland
Jan 17
Un des leaders de l'industrie pharmaceutique, une biotech innovante et en perpétuelle évolution, est à la recherche d'un Associate Director pour le département de l'International Regulatory Strategy. C'est une entreprise reconnue, possédant un excellent portefeuille de produits. Pour cette opportunité, nous recherchons un candidat parlant couramment anglais, avec un background en neurosciences ou maladies génétiques.
Regulatory Affairs Coordinator - Medical Devices
Paris
Jan 17
ProClinical are currently seeking Regulatory Affairs Coordinators based in Paris, France for a global medical devices project. There are also opportunities in Madrid, Lisbon, Rome, Athens or Tel Aviv.The global medical devices project will require Coordinators to collect Regulatory data and coordinate projects, liaising with Regulatory Affairs, Marketing, Supply Chain etc. The position will give an excellent opportunity for a junior profile to progress in their career. ...
Manager Regulatory Affairs (m/w) Medizintechnik
Karlsruhe
Jan 17
Manager Regulatory Affairs (m/w) Medical DevicesOffice-based in der Nähe von KarlsruheAufgaben:- Erarbeitung und Umsetzung von Zulassungsstrategien und –plänen für neue Produkte weltweit. ...
AD/Director, Data Sciences, Safety and Regulatory (DSSR) Business
reading
Jan 17
PURPOSE Establish and manage an effective Sales plan to maximize Organizational growth for the allocated Business unit(s) for Data Sciences, Safety & Regulatory (DSSR) services in the relevant Geography. To serve as strategic business partner responsible for identifying, developing and expanding new business opportunities in alignment with internal stake holders within Sales, Account Management & Operations (BU & GDN). ...
Associate Director - Regulatory Affairs
USA
Jan 17
My client is an emerging bio-pharmaceutical company whose pipeline spans multiple therapeutic areas through strategic alliances, collaborations and partnerships with academic institutions and pharmaceutical companies.
Regulatory Specialist- world well known Cosmetic Brands
Germany
Jan 17
Regulatory Specialist- world well known Cosmetic Brands My client a global leader and one of the fastest growing entities within the Cosmetic Industry is currently looking for a Regulatory Affairs Manager to join one of it departments in Germany.Products manufactured by my client belong to some of the most famous brands in the world. World leading company gives you an opportunity to work with best specialists within the field and expand your professional network. ...
CMC Regulatory Specialist –Interesting Pipeline- Belgium
Antwerp
Jan 17
A biotech company is looking for a CMC Regulatory Specialist to complement the regulatory team on the CMC part of the dossier (the others are more (pre)-clinical focused). The company has no products on the market yet and has a strong pipeline which means you can be part of the process from pre-marketing stage and have more impact on the company's success by bringing innovative products to the market.
SSU and Regulatory Specialist I - Study Start Up (South Africa)
Johannesburg
Jan 17
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
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