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The latest Regulatory jobs - BETA

Jobs: (Regulatory)

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Regulatory Affairs Associate - Medical or IVD Experience - X4 Group
London
Apr 21
I am looking for a Technical Writer for a Medical Device Company based towards London. You are required to have experience in Regulatory Affairs and will be working predominantly on Technical Files and some Risk Management work. ...
Regulatory Affairs Officer
Belgium
Apr 21
Regulatory Affairs OfficerDuration: 8 month contract Location: Belgium, Antwerp RegionRate: €41 - €49 per hourI’m looking for an independent consultant to work on an 8 month contract initially, for my client in Belgium.My client is one of the largest pharmaceutical company. They develop therapies and treatments to improve the lives of their patients across a range of therapy areas including oncology, CNS, immunology, and diabetes areas. ...
Regulatory Affairs Officer
Antwerp
Apr 21
Regulatory Affairs Officer8 month contract (good potential to extend)Belgium, Antwerp Region€42 - €48 per hourI’m seeking a contractor to work on an 8 month assignment initially, for my client in Belgium.My client is a well-recognised pharmaceutical company. They develop therapies and treatments to improve the lives of their patients across a range of therapy areas including oncology, CNS, immunology, and diabetes areas. ...
Senior Regulatory Affairs Consultant
Dublin and flexible
Apr 21
On behalf of my client, a regulatory affairs consultancy firm, I am recruiting for a Senior Regulatory Affairs Consultant.
Regulatory Affairs Specialist
Hertfordshire
Apr 21
Regulatory Affairs Specialist Location: Hertfordshire Duration: Initial 6 month contract My client is a global leader in the healthcare industry, with a long term commitment to research and development.
Regulatory Officer
Oxfordshire
Apr 21
A superb new opportunity has arisen with a growing international CRO. They are currently searching for a Regulatory Officer to join their team in the UK. This is an important position within the organisation which will allow for key interaction between Clinical and Regulatory team.
Regulatory Affairs Manager (m/w) Hemophilia
Switzerland
Apr 21
Regulatory Manager, Development Products (m/w) Biotechnology Office-based in Switzerland, full-time Job Description: - Develop the Regulatory strategy for new and for licensed products in Europe for applications via centralized and national procedures (DCP, MRP). - Communicate and ensure the implementation of the European Regulatory strategy in global teams. ...
Regulatory Affairs Manager (m/w)
Switzerland
Apr 21
Regulatory Affairs Manager (m/w)Office-based in der Schweiz Vollzeit- unbefristetAufgaben:- Durchführung technischer Dokumentationen für Medizinprodukte - Unterstützung der einzelnen Fachbereiche bei allen fachspezifischen Anliegen- Identifizieren regulatorischer Anforderungen - Führung eines Teams von 3 Personen- Entwicklung von Prüf-, und Zulassungsstrategien - Durchführung und Begleitung externer und interner Audits- Sicherstellung des Erfüllens internationaler Zulassungsno ...
Regulatory Affairs Manager (m/w)
Baden-Württemberg
Apr 21
Regulatory Affairs Manager (m/w)Office-based in Baden-WürttembergAufgaben:- Technische Dokumentation der Unterlagen für die Zulassung - Prüfung und weitere Bearbeitung von Zulassungen von Medizinprodukten im nationalen und internationalen Umfeld- Teilnahme an internen Audits- Enge Zusammenarbeit mit dem Bereich Entwicklung- Leitung und Pflege des QMS - Verantwortung für das ReklamationswesenVoraussetzungen:- Studium der Medizintechnik oder vergleichbares Studium- 1-2 Jahre Erfahrungen in der ...
Regulatory Affairs Director
Paris
Apr 21
Director of Regulatory AffairsLocation : ParisDuration : permanent Permanent role, full timeMain responsibilities:- Collaborating with responsible departments for regulatory submissions - Developing standard operations procedures - Assisting the regulatory team in developing regulatory strategies - Leading interactions with the European authorities- Assisting internal team- Manging regulatory projects and specific timelines - Monitoring emerging legislation and guidance and contributing to e ...
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Regulatory Affairs Administrator
Scotland
Apr 21
This position supports both the Regulatory Affairs team and the Department Head.
Senior Regulatory Affairs Specialist
Somerset, NJ
Apr 21
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at 617 982 1238 today!
Manager, Regulatory Affairs
Piscataway, New Jersey
Apr 21
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at 617 982 1238 today!
Regulatory Manager
United States
Apr 21
TalentSource Life Sciences is currently searching for a Regulatory Manager to work with one of our partner pharmaceutical companies in the United States.   This is freelance position for 0.8 FTE and will be home based. The successful candidate will be working on studies dedicated to one client.     TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions.
Regulatory, Quality and Compliance Admin - Uxbridge
Uxbridge
Apr 20
Lucy Stendall is recruiting for a Regulatory, Quality and Compliance Administrator to join a Global Biopharmaceutical company at their site based in Uxbridge, West London...
Associate Director - Regulatory Affairs - Can work remotely and flexible working hours. Great regulatory work in a company with great work ethic
Oxfordshire
Apr 20
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Manager - Great consultancy with some remote working and flexible hours - Oxfordshire
Oxfordshire
Apr 20
To apply for this Regulatory Affairs Manager please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Champion
Madrid
Apr 20
PURPOSE  We seek for candidates providing regulatory support and oversight for our operational team. Responsibilities Collate regulatory document- and process requirements for countries under responsibility. Assist with creation and/or review of country-specific regulatory documentation to enable study initiation and maintenance, as required. ...
Study Start up - Regulatory Submissions Coordinator
Kiev
Apr 20
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. ...
Coordinator Regulatory Affairs
Brussels
Apr 20
Location : BrusselsStart date : As soon as possible Contract position, full time, office basedDuration : 5 to 6 months contract position Main responsabilities :- Providing regulatory administrative support and coordination for the department with maintenance of tracking systems and databases- Preparing submissions and renewals and maintenance of local files- Ensuring the artwork including all package components - Assisting in compilation and submission of regulatory documents to the local re ...
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Regulatory Affairs Manager (m/w) International
Berlin
Apr 20
International Regulatory Affairs Manager (m/w)Office-based in BerlinYour tasks:You are responsible for the acquisition and regulatory management of international marketing authorizations for medical devices, food supplements and cosmetics. This involves conducting all necessary activities to maintain existing or acquire new authorizations, registrations and certifications in the Eastern European and CIS countries where our products are marketed. ...
Manager, Regulatory Affairs Strategy- Oncology
New Jersey
Apr 20
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at 617 982 1238 today!
Regulatory Affairs Project Manager - Maidenhead
Maidenhead
Apr 20
Oliver Care is recruiting for a Regulatory Affairs Project Manager in Emerging Markets to join a company in the pharmaceutical industry at their site based...
Regulatory Affairs Officer
Belgium
Apr 20
Regulatory Affairs Officer Antwerp Area, Belgium Start date: 1/05/2017   TalentSource Life Sciences, the division of CROMSOURCE dedicated to flexible staffing solutions, is currently recruiting for a Regulatory Affairs Officer to strengthen the team of one of our Top 10 Pharmaceutical Companies.         Responsibilities This position is responsible for the management and delivery of regulatory submissions required to support the development,...
Regulatory Affairs Manager
High Wycombe
Apr 19
My client, the world leader in Biopharma products, is currently recruiting for an exciting new position of a Regulatory Affairs Manager to help them develop their Oncology strategy as they face a year of rapid growth. This is a perm role based in High Wycombe and the ideal role for a candidate that is keen to pursue a more senior step in their career.
Regulatory Associate
Hertfordshire
Apr 19
An internationally known pharmaceutical company situated in Hertfordshire, UK and operating in over 150 markets worldwide is looking to hire a Regulatory Associate. The company develops a broad range of products in pharmaceuticals, vaccines and consumer healthcare. ...
Regulatory Affairs Manager (m/w) in Basel
Basel
Apr 19
Regulatory Affairs Manager (m/w) in Basel Zur Verstärkung des Regulatory Affairs Teams in Basel suchen wir zum nächstmöglichen Zeitpunkt eine/n Regulatory Affairs Manager (m/w) mit folgenden Aufgabenbereichen. ...
Regulatory Affairs CMC Project Manager - Drug Development
France
Apr 19
Regulatory Affairs CMC Project Manager - Drug Development - Small Molecule
Regulatory Affairs Manager
München (81249)
Apr 19
ewi Life Sciences are proud to partner with a leading global optical instrument medical device company.With continued growth throughout the business we are looking for Regulatory Affairs Managers who have experience of working with active/electronic medical devices.I am keen to speak to those individuals who have particular experience with working with optical or optoelectrical companies in the past who want to part of something exciting.Candidate must be fluent in German and English.
Team Leader Regulatory Affairs (m/w)
Stuttgart
Apr 19
Teamleader Regulatory Affairs (m/w)Office-based in Stuttgart Vollzeit- unbefristetAufgaben:- Durchführung technischer Dokumentationen für Medizinprodukte - Unterstützung der einzelnen Fachbereiche bei allen fachspezifischen Anliegen- Identifizieren der Weltweiten regulatorischen Anforderungen - Führung eines Teams- Entwicklung von Prüf-, und Zulassungsstrategien - Durchführung und Begleitung externer und interner Audits- Sicherstellung des Erfüllens internationaler Zulassungsn ...
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Labeling Compliance and Regulatory Specialist
Basel
Apr 19
Post-grad with experience in regulatory affairs wanted for our pharma client in Basel, Switzerland.
(URGENT) Regulatory, Quality and Compliance Administration Assistant Required – 12 Month Contract…
London Area
Apr 19
(URGENT) Regulatory, Quality & Compliance Administration Assistant Required – 12 Month Contract…
Global Regulatory Affairs Lead
Amsterdam,Netherlands
Apr 19
The Global Regulatory Lead (GRTL) is a member of the Global RA Strategy Team and reports directly to the Global RA Head of Product Development & Strategy. This role is responsible for providing strategic vision and innovative scientific and regulatory leadership in defining and executing the global regulatory strategy through all clinical phases of product development for the assigned product/product portfolio. Position is based in Amsterdam.
Sr. Specialist, Regulatory Affairs
Bridgewater, NJ
Apr 19
The Regulatory Affairs Senior Specialist executes the pharmaceutical regulatory strategies for assigned products. Supports the Regulatory Affairs Senior Manager with regard to submissions and other product development and support activities.
Regulatory Manager. UK. Hertfordshire
Hertfordshire
Apr 19
Regulatory Manager UK. Office based. Hertfordshire Area Fast growing Oncology based industry client seeks an experienced industry Regulatory Manager
Director, Regulatory Affairs
Bridgewater, NJ
Apr 18
The Regulatory Director coordinates and oversees regulatory development and post-approval regulatory activities for US generic (Gx) products.
Associate Director, Regulatory Affairs-CMC
Bridgewater, NJ
Apr 18
The Regulatory Affairs – CMC Associate Director independently manages all regulatory CMC aspects of company Pharmaceuticals products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, Dietary Supplements and Medical Devices. The Associate Director is responsible for the regulatory CMC strategies of all submissions for products under his/her responsibility as well as managing interactions with regulatory authorities on CMC issues.
Regulatory Officer
Hampshire
Apr 18
An exciting Regulatory Affairs Associate job opportunity for a proactive life science graduate to work in a growing British pharmaceutical company based in South Hampshire....
Regulatory Affairs Senior Manager
Sofia city
Apr 18
A Fantastic opportunity for a Regulatory Affairs Senior Manager to join a dynamic, fast growing Pharmaceutical Consultancy where you will be responsible for managing projects...
Regulatory Affairs Assistant
Leeds
Apr 18
A leading multinational pharmaceutical, and medical devices company currently has an attractive job vacancy available for a Regulatory Affairs Assistant to be based in their office in Leeds, UK. ...
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Regulatory Affairs Junior Manager
Sofia district
Apr 18
A Fantastic opportunity for a Junior Regulatory Affairs Manager professional or an ambitious Life Science graduate to join a dynamic, fast growing Pharmaceutical Consultancy where...
Regulatory Affairs Specialist
Switzerland
Apr 18
This Regulatory Affairs Specialist job is with one of the most renowned global pharmaceutical, medical device and consumer health organisations located in Switzerland. The organisation is a top 10 pharma company and employs over 100,000 professionals worldwide.Job Role: Drawing on relevant expertise and information from internal and external sources, make a major contribution towards the preparation of regulatory documentation (e.g. Technical Files). ...
Regulatory Affairs Manager (m/w)
Sindelfingen (71063)
Apr 18
Regulatory Affairs Manager (m/w)Office-based in Sindelfingen Vollzeit/ unbefristetAufgaben:- Erstellung der technischen Dokumente für die nationale und internationale Zulassung- Ausarbeitung und Erstellung der Dokumente für nationale und internationale Zulassung- Aufbereitung und Umsetzung regulatorischer Anforderungen- Kommunikation mit internen und externen Ansprechpartnern- Schnittstelle für alle angrenzenden Fachbereiche hinsichtlich regulatorischer FragenVoraussetzungen:- Studium der M ...
Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
Apr 18
Tec Group international has partnered with a global Pharmaceutical company to find a regulatory profile to help lead the business and Regulatory departments. This position offers a creative platform for the chosen candidate to work on projects and areas they excel in. This position is based in Boston and offer a competitive salary and package. For more info please contact Sam Murphy at TEC Group sam.murphy@tecgroup.net
Associate Director, Global Regulatory Affairs; Immuno-Oncology
USA
Apr 18
For more info please call Sam Murphy on 0044 208 544 3423 / sam.murphy@tecgroup.net
SSU and Regulatory Specialist II (Bulgaria)
Bulgaria
Apr 18
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.
Regulatory Affairs Officer
East Midlands
Apr 18
An excellent opportunity has arisen for a Regulatory Officer with 1-3 years of experience to join a leading Pharmaceutical company based in East Anglia.
Senior Medical Writer - Regulatory UK
Wales
Apr 18
I am looking for an experienced Regulatory Medical Writer to join a market leading and prestigious consultancy. This opportunity will allow you to lead projects with international clients. In this role you will also be able to contribute to the success of the company by having your opinion heard. The service you will provide is more than just writing, you will be an essential part of the clinical development teams across different therapeutic areas.
Regulatory Affairs Consultant - SLOVAKIA
Slovakia
Apr 18
Skills Alliance have partnered with a rapidly growing pharmaceutical company for the Regulatory hiring on their Slovakian site.One urgent requirement is for an experienced...
Regulatory Affairs Director (Global Strategy)
Geneva
Apr 18
My client, a mid-sized innovator pharmaceutical company, is seeking a Director of Regulatory Affairs to provide leadership to a team and continue the growth of the business. This regulatory affairs role is based in Geneva, Switzerland on a permanent basis. ...
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Regulatory Affairs Officer - Pharmaceuticals
Beerse, Antwerp, Belgium
Apr 18
Regulatory Affairs Officer / Beerse, Belgium / 7 Months Contract / 38 to 48 EUR (Per Hour)
Regulatory Affairs Associate
Mahwah
Apr 18
Looking for Regulatory Affairs individuals who are interested in working with a growing pharmaceutical company. This is a contract to hire opportunity with incredible benefits....
Medical Writer (Regulatory)
Edison
Apr 14
Medical Writer (Regulatory) Location: Edison NJ Area Salary: Competitive Industry: Pharmaceuticals Job Type: Contract – 12 months Responsibilities:
Regulatory Affairs Specialist (Medical Devices) / global, international Company
Stuttgart
Apr 13
A unique Regulatory Affairs Specialist job for an organised Regulatory Specialist in a global operating company for Medical Devices in Classes 1 – 3. This...
Head of Regulatory Affairs / QA - aufstrebender Mittelstand nahe Erfurt
Erfurt
Apr 13
Eine einzigartige Chance als Regulatory Affairs Manager fuer Medizinprodukte Teil eines internationalen Teams bei einem fuehrenden Hersteller fuer Spezialprodukte der Medizintechnik zu werden. Wir suchen...
Director QA and Regulatory Affairs (m/w) Europe
Baden Württemberg
Apr 13
Eine einmalige Chance als Ingenieur und Regulatory Affairs Spezialist im Bereich medizinische Geraete der Klassifizierungen 1 bis 3, Teil eines global operierenden Unternehmen zu werden....
Quality and Regulatory Manager
West Midlands
Apr 13
Quality Manager / QA RA Manager / Quality and Regulatory Manager Location: West MidlandsSalary: £35,000 - £45,000 DOE potential to be flexible I am currently working with a Medical Device Manufacturing Company who are seeking a Quality & Regulatory Manager to join their team on a permanent basis. This is a small company who are working on a range of developing products. ...
Regulatory Submissions Coordinator
Denmark
Apr 13
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. ...
Regulatory Submissions (Study Start-up) Manager
München (81249)
Apr 13
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Regulatory Submissions Coordinator
München (81249)
Apr 13
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. ...
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Sr SSU and Regulatory Specialist (Ukraine)
Ukraine
Apr 13
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.
Regulatory Affairs Expert
Baden-Württemberg
Apr 13
Regulatory Affairs Expert (m/w)Office-based in Baden- WürttembergAufgaben:- Erstellung der technischen Dokumentation für die Zulassung von Medizinprodukten- Prüfung und Überarbeitung der Anforderungen der regulatorischen Vorgaben - Kommunikation mit den zuständigen Behörden - Einreichung der Dokumente- Durchführung interner Audits- Ansprechpartner in allen zulassungsspezifischen Fragen für die angrenzenden Fachbereiche- Entwicklung von ZulassungsstrategienVoraussetzungen:- Studium mit techni ...
Regulatory Affairs Manager (m/w)
Karlsruhe
Apr 13
Regulatory Affairs Manager (m/w)Office-based in Karlsruhe – Vollzeit, unbefristetAufgaben:• Erstellung bis hin zur Einreichung der Zulassungsdokumente bei den zuständigen Behörden (CE/ FDA)• Optimierung des QMS• Durchführung von Gebrauchstauglichkeitstests• Vorbereitung und Durchführung von internen und externen Audits• Ansprechpartner in allen zulassungsbedingten Belangen Voraussetzungen:• Studium der Medizintechnik oder vergleichbar• Kenntnisse in nationalen und internationalen Zulassungs ...
SSU and Regulatory Specialist (Poland)
Poland
Apr 13
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.
Associate Director, Regulatory Affairs, CMC
London
Apr 13
My client is a small pharmaceuticals company based centrally in London. They have a requirement for a very experienced Regulatory Affairs professional highly experienced with CMC to work from their modern London office in a highly strategic environment. Candidates looking for a very professional and well run business, with a very strong pipeline of products and growing global presence should apply.
Regulatory Manager
Buckinghamshire
Apr 13
Regulatory ManagerA fantastic opportunity for a Regulatory Professional to join a global Pharma. You will act as Regulatory Lead on EU Submissions for life-cycle. You will prepare and review Regulatory submissions for post-approval.All candidates must be eligible to work in the UK. ...
Regulatory Manager - Post Approval
Essex
Apr 13
Regulatory Manager - Post ApprovalMy client, a rapidly growing Regulatory consultancy is looking for an experienced professional with a strong background in post-approval Regulatory to manage a team of Regulatory Associate/Senior Associates. Excellent opportunity to join a rapidly growing consultancy with a clear defined path to Director.Job Title: Regulatory ManagerLocation: Commutable from Cambridge or North East London.Benefits: Very good annual salary + benefits + bonus. ...
Associate Director Regulatory Affairs-Maidenhead
Maidenhead
Apr 13
Oliver Care is recruiting for an Associate Director Regulatory Clinical Trials to join a company in the Pharmaceutical industry at their site based in Maidenhead...
Regulatory Affairs Senior Consultant
High Wycombe
Apr 13
Job Role:The Regulatory Professional provides support to the EMEA Regulatory Liaison (EURL)/EMEA Regional Therapeutic Area Leader and/or Global Regulatory Leader (GRL) for regulatory activities for products in the assigned portfolio. ...
Manager, Regulatory Records
Camberley
Apr 12
Do you want to be a 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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Senior Regulatory Affairs Manager - North West
North West
Apr 12
My client is a young dynamic SME with award winning products that is now looking for a Senior Regulatory Affairs Manager to head up a team of 7 and help develop new projects to continue this company’s success. The perfect candidate will be an established Regulatory Manager that has previously been hands on with a small to medium team previously with a proven history of success in Regulatory Affairs from within the medical Devices industry.
Regulatory Affairs Medical Writer – Permanent – homebased - Up to 60k - Europe - CSRs/CTDs
Home-based
Apr 12
Permanent opportunity to work for a Leading US CRO, whilst being home based in Europe. Looking for experienced Regulatory writers, comfortable with Clinical study reports (CSRs), protocols, investigator brochures etc. Chance to get involved in projects from varied clients in a growing business.
Regulatory Medical Writer – Full time – Up to 60k – Home-based – Europe – Global CRO
Home-based
Apr 12
A midsized CRO with an International presence is seeking a Regulatory Medical Writer to join their prestigious Medical Writing team. With a long list of high profile clients and extensive project opportunities, they have established an impressive reputation within this industry.
Regulatory Medical Writer
West Sussex
Apr 12
My client is seeking a motivated individual with a science, research, publishing and / or medical writing background who would like the opportunity to help them build their medical writing team and be involved in the development of new products being evaluated for the treatment of cancer.
Regulatory Affairs Manager
Altstätten S G
Apr 11
My client is a leader in dental medical devices. They have enjoyed continued success in the EU, US, Canadian and Latin American markets and are...
Regulatory Affairs Manager
Munich
Apr 11
My client is looking for Regulatory Affairs Manager based near Munich - Germany. This is a very exciting opportunity to work with rapidly growing medical device...
International Regulatory Affairs Specialist - Medical Devices
Switzerland
Apr 11
International Regulatory Affairs Specialist - Medical Devices - Based in Switzerland
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AD/Director Regulatory Affairs, Labeling
San Diego
Apr 11
A leading opportunity to join an innovative and established development biotechnology company based locally to Sand Diego, CA.

Role:
To write, submit, and maintain labeling...
Associate Director Regulatory Affairs
Slough
Apr 11
*****Associate Director Regulatory Affairs- Medical Devices- Berkshire*****
Regulatory Documentation Scientist required for Global Pharmaceutical Company based in Hertfordshire…
Hertfordshire
Apr 11
Regulatory Documentation Scientist required for Global Pharmaceutical Company based in Hertfordshire…
Senior Manager Regulatory Affairs - Hatfield
Hatfield
Apr 11
Oliver Care is recruiting for a Senior Manager Regulatory Affairs to join a company in the Pharmaceutical industry at their site based in Hertfordshire on...
Regulatory Affairs Director - Hatfield
Hatfield
Apr 11
Oliver Care is recruiting for a Director Regulatory Affairs to join a company in the Pharmaceutical industry at their site based in Hertfordshire on a...
Regulatory Consultant- Oncology
High Wycombe
Apr 11
*****6 Month Regulatory Contract- Oncology Filing- Big Pharma- Bucks*****
Regulatory Affairs “CMC ” EU and Global CONTRACT Roles – up to £70 per hour – Large molecule/Biotechnology projects...
Maidenhead or Uxbridge
Apr 11
We do offer an iPad 3 for any referrals that we help to place in a new role, so if this role isn’t for you but you do have colleagues past or present who are looking please consider referring the individual to us – many thanks….”
New Regulatory “CMC Bio Writer Role” - CONTRACT - Maidenhead or Uxbridge – to £70 per hour - Options to work from Home
Maidenhead or Uxbridge
Apr 11
This contract is paying up £70 per hour for either 6 or 12months where you will be providing CMC writing support for NBE/biologicals in Phase1 and Phase 2 whilst reporting into an experienced and likable RA Director who will give you flexible working hours and some options to work 1-2 days from hom
Regulatory Affairs Associate Director Role – East Coast OR Work from Home – Team Leadership and full Strategic responsibility for a mixed portfolio
East Coast OR Work from Home
Apr 11
You will represents Regulatory Affairs in multi-disciplinary project / brand teams with accountability for the regulatory plan, leading a team of strong regulatory performers - This is a great opportunity to join their expansive and highly regarded regulatory team in a role where you can utilize your strong leadership experience and where regulatory is seen as a valued, strategic partner.
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Regulatory Affairs Snr Manager – East Coast/North Carolina OR work from Home - Join an expanding Pharma Co. - Grow and develop your strategic expertise
USA
Apr 11
This organisation is one that I’m sure will be able to present you with the next steps in your regulatory career – but they do want RA professionals who are strong, motivated and ready to take real responsibility and leadership of their projects.
Senior Regulatory Affairs Manager required for global generics company based near London…
London Area
Apr 11
Senior Regulatory Affairs Manager required for global generics company based near London…
Regulatory Affairs Managers needed for fantastic generics company based around London…
Hertfordshire
Apr 11
Regulatory Affairs Managers needed for fantastic generics company based around London…
Regulatory and Site Services Specialist
Spain
Apr 11
We are looking to recruit a Regulatory and Site Services Specialist - office based in Madrid
Senior Manager Advertising and Promotional Compliance Regulatory Affairs
Princeton, NJ
Apr 10
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at (646) 586 9087 today!
International Regulatory Affairs Manager - Pharmaceutical
Portugal
Apr 10
International Regulatory Affairs Manager - Pharmaceutical - EMA, FDA and Emerging market
Regulatory Associate
Uxbridge
Apr 10
Regulatory and Site Services Specialist (W/M) - Madrid, Spain
Spain
Apr 10
We are looking to recruit Regulatory and Site Services Specialist office based in our Chiltern Office in Madrid.
regulatory jobs : 100 +
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