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The latest Regulatory jobs - BETA

Jobs: (Regulatory)

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Regulatory Program Manager
United Kingdom
Apr 29
TalentSource Life Sciences is currently searching for an experienced Regulatory Program Manager to work with one of our partner pharmaceutical companies in the Hertfordshire area.     This is a temporary position with TalentSource for 12 months with the possibility of being extended, on a full time basis. The successful candidate will be working on studies dedicated to one client.
Regulatory Affairs Specialist Maternity Leave Contract
Limerick, Republic of Ireland
Apr 28
Our client, a global medical devices company currently have a vacancy for a Regulatory Affairs Specialist. The Regulatory Affairs Specialist helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets. The regulatory affairs specialist serves as a communication liaison between the company manufacturer and the company local affiliates or regulatory authorities.
Regulatory Associate II
Berkshire
Apr 28
Regulatory Associate II CMCA fantastic opportunity for a candidate with Regulatory experience but looking to further their career in CMC to join a global CRO. With support and training you will prepare and review CMC regulatory submissions and have CMC responsibility for a portfolio of assigned products. ...
Regulatory Associate
Berkshire
Apr 28
Regulatory Associate CMCA fantastic opportunity for a candidate with Regulatory experience but looking to further their career in CMC to join a global CRO. With support and training you will prepare and review CMC regulatory submissions and have CMC responsibility for a portfolio of assigned products. ...
Regulatory Affairs/ Quality Manager (m/w)
Hamburg
Apr 28
Regulatory Affairs/ Quality Manager (m/w)Office-based in Hamburg – vollzeit/ unbefristetAufgaben:- Erarbeitung von Registrierungsstrategien, sowie die Teilnahme und Mitarbeit in Design Reviews- Sicherstellung der Einhaltung folgender Richtlinien: MDD, FDA, - Berücksichtigung des Produktentwicklungsprozess- Erstellung, Prüfung und Freigabe der Dokumente innerhalb des Regulatory- Bereichs- Koordination, Zulassung und Aufrechterhaltung aller essentiellen Regulatory- Affairs- Aktivitäten und Int ...
Team Leader Regulatory Affairs (m/w)
Brandenburg
Apr 28
Team Lead Regulatory Affairs (m/w)Office-based in Brandenburg vollzeit- unbefristetAufgaben:- Dokumentation, Prüfung und weitere Bearbeitung von Zulassungen von Medizinprodukten im nationalen und internationalen Umfeld- Abstimmung und Mitarbeit mit dem zuständigen Fachbereich bis hin zur Markteinführung- Verantwortungsvoller Aufbau des RA Bereichs- Vorbereitung und Durchführung von internen und externen Audits- Durchführung von Schulungen hinsichtlich regulatorischer NeuerungenVoraussetzunge ...
Head of Regulatory Affairs (m/w)
Stuttgart
Apr 28
Head of Regulatory Affairs (m/w)Office-based in Stuttgart vollzeit- unbefristetAufgaben: - Erarbeitung und Umsetzung von Zulassungsstrategien und –plänen für neue Produkte weltweit.- Koordination und Erstellung von Produktakten für EU und weltweite Zulassungen- Definition und Erstellung von Produktkennzeichnung (Label) und Gebrauchsinformationen (IFU)- Unterstützung und Zusammenarbeit bei der Erstellung von Prüf- und Validierungsplänen. ...
Regulatory Manager CTA
England
Apr 28
Regulatory Manager CTA - Home-basedMy client, a leading Regulatory Affairs consultancy, is looking for an experienced candidate to join their development team as a Regulatory CTA Manager. This could suit a Senior Associate looking to make the transition to management. This position can be offered fully home-based. ...
Regulatory Manager CTA
England
Apr 28
Regulatory Manager CTAMy client, a leading Regulatory Affairs consultancy, is looking for an experienced candidate to join their development team as a Regulatory CTA Manager. This position can be offered fully home-based. ...
Regulatory Affairs Manager (EU) GI
Buckinghamshire
Apr 28
We are looking for a Regulatory Affairs Manager with our client in Buckinghamshire to start ASAP working in GI. This is a full time - permanent role. Competitive rate of pay - full details on application
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URGENT: Regulatory Affairs and Information Officer Consultant – Germany
Germany
Apr 28
Just Pharma are seeking an established Regulatory Affairs and Information Consultant on behalf of their client in Germany.
Regulatory Affairs Officer - Munster - Flexibility for full-time or part-time
Munster, Republic of Ireland
Apr 28
Our client, a pharmaceutical company now have an immediate requirement for a Regulatory Affairs Officer. This is to be based in Munster, Ireland. The company are open to candidates working full-time or part-time.
Senior Regulatory Affairs Manager - Great consultancy with some remote working and flexible hours - Oxfordshire
Oxfordshire
Apr 27
To apply for this Regulatory Affairs Manager please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
REGULATORY AFFAIRS MANAGER (MDandD) - UK/EU - PERMANENT ROLE
UK or EU home based
Apr 27
Regulatory Affairs Manager with expertise in MD&D required to build MD&D arm of regulatory affairs department in specialist CRO. UK or EU, home based.
Associate Director, Global Regulatory Affairs; Immuno-Oncology
USA
Apr 27
For more info please call Sam Murphy on 0044 208 544 3423 / sam.murphy@tecgroup.net
Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
Apr 27
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
Regulatory Affairs Manager - San Fran
bay area
Apr 27
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
Clinical Submission/Regulatory Expert
Munich
Apr 27
Unsere Kundin, eine globale Top 10 CRO, sucht eine/n Senior CRA oder Junior CTM, der/die in einer Submission/ Regulatory Expert-Position arbeiten möchte. Die Position ist office-based in München bei einem Sponsor. ...
Regulatory Affairs Officer
Berkshire
Apr 27
Our client is a pharmaceutical manufacturing and marketing company based out of the United Kingdom. They provide a variety of services from manufacturing to R&D through UK based facilities and several global partnerships. They are seeking a Regulatory Affiars Officer to be based in Berkshire, UK.Job Responsibilities: Prepare and submit applications of reliable quality in a timely manner to MHRA (UK) via National Procedure. ...
Regulatory Affairs Specialist / Medical Devices / RA / RA Specialist / Post Market Surveillance / PM
Berkshire
Apr 26
Job Title: Senior Regulatory Affairs SpecialistLocation: BerkshireSalary: £35,000 - £42,000 Depending on Experience I am currently working with a global recognised Medical Device company based in Berkshire who are looking for a Senior Regulatory Affairs Specialist to join the team.Some of the Key Activities & Accountabilities:The medical device company are seeking a Senior Regulatory Affairs Specialist (Post Market) to work in the UK distribution site based in Berkshire. ...
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GSK Consumer Healthcare - Regulatory Affairs Associate Benelux
Belgium
Apr 26
Job Purpose: • Getting quality products* to the market with optimal claims and keeping them there, by knowing relevant legislation and complying/respecting to it. • Providing product-related quality information to other departments, authorities, consumers, health care professionals and trade associations.
Manager, Global Regulatory Affairs
Belgium
Apr 26
Position holder (PH) will have global responsibility (for Regulatory Affairs) of given activities for a Project/Product within GSK Vaccines.
Manager Non-clinical Pharmacology Global Regulatory Affairs
Belgium
Apr 26
The Manager, non-clinical pharmacology, GRA, will have responsibility for the coordination, writing and the preparation of the non-clinical pharmacology regulatory documents (CTD, IND, CTA, , Q&A, etc) during vaccine development, for new submissions, and during product lifecycle.
Lead Regulatory Affairs Specialist - Biocides - EMEA role - Great new role for the new year
Midlands
Apr 26
To apply for this regulatory affairs specialist role please call Julie Cooper on 07951 082482 or alternatively please send your CV to :julie@mosaicrecruitment.co.uk in the strictest confidence.
Near beautiful Canal City GHENT - Regulatory Manager - Medical Devices - NPD , Strategy and Compliance - International role
Belgium
Apr 26
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
EMEA Regulatory Affairs Specialist - Medical Devices
Malta
Apr 26
EMEA Regulatory Affairs Specialist - Medical Devices - Development and post market
Senior Regulatory Affairs Manager - Great consultancy with some remote working and flexible hours - Oxfordshire
Oxfordshire
Apr 26
To apply for this Regulatory Affairs Manager please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Some remote working and flexible hours.Great variety of work and work for a company that is different.
Oxfordshire
Apr 26
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Global Regulatory Labelling Director - US and EU experience - Lead a team - Part remote working available- Central London
London
Apr 26
To apply for this Regulatory Affairs Labelling Director please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Medical Writer Germany
Germany
Apr 26
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.
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Senior Regulatory Affairs Associate / Manager - CTA
South East
Apr 26
Senior Regulatory Affairs Associate / Manager - CTA Location: East London/Cambridge/Essex Salary: up to £52,000 per annum + benefits + Both Quarterly and Annual bonus Reference: J28368
Regulatory Associate - Ware, UK
Ware
Apr 26
EZ/5781Regulatory AssociateWare, HertfordshireOffice-based Here at inVentiv Health Clinical we are currently recruiting for a regulatory professional to work fully embedded with our pharmaceutical sponsor as a Regulatory Associate office based in Ware.This role can be offered either as a permanent contract of employment or as a 12 months freelance contract.inVentiv Health: Work Here. Matters Everywhere. ...
Regulatory affairs specialist
West Midlands
Apr 26
A medium sized diagnostic company are offering the opportunity for an experience regulatory professional to work on variety
Regulatory Affairs Associate Director
Berkshire
Apr 26
Regulatory Affairs Associate Director Location: Berkshire Salary: £70,000 - £85,000 per annum depending on experience + pension, healthcare, bonus, 25 days holiday, life assurance Reference: J28371
Senior Manager \ Associate Director Regulatory Affairs
Berkshire
Apr 26
Senior Manager \ Associate Director Regulatory Affairs: Berkshire Salary: £65,000 - £85,000 per annum depending on experience + pension, healthcare, bonus, 25 days holiday, life assurance Permanent
Regulatory Affairs Specialist
Billerbeck
Apr 26
My client is a leader in surgical, implantable medical devices. Their continued success has led to expansion, and they now require a Regulatory Affairs Specialist. ...
Regulatory Affairs Senior Specialist
Switzerland
Apr 26
A global leading Medical Devices company is currently looking for a Regulatory Affairs Senior Specialist for its Swiss site. This could be for you a great opportunity to get into an well-established company and therefore continue to develop your expertise with an international exposure.
Associate Director Regulatory Affairs
Cambridge
Apr 26
Regulatory Director SummaryAre you an experienced Regulatory professional with a background in CMC (small molecule or biologics) looking to move into a massively expanding Consultancy to lead a small team of Consultants and act as Regulatory lead on projects? Due to the expansion of the group they are looking to recruit an experienced Regulatory Professional to manage a small team and act as lead on some very interesting projects. ...
Director of Regulatory Affairs
Cambridge
Apr 26
Director of Regulatory AffairsSummaryAre you an experienced Regulatory professional with a background in CMC (small molecule or biologics) looking to move into a massively expanding Consultancy to lead a small team of Consultants and act as Regulatory lead on projects? Due to the expansion of the group they are looking to recruit an experienced Regulatory Professional to manage a small team and act as lead on some very interesting projects. ...
Regulatory Director
Cambridge
Apr 26
Regulatory Director SummaryAre you an experienced Regulatory professional with a background in CMC (small molecule or biologics) looking to move into a massively expanding Consultancy to lead a small team of Consultants and act as Regulatory lead on projects? Due to the expansion of the group they are looking to recruit an experienced Regulatory Professional to manage a small team and act as lead on some very interesting projects. ...
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Regulatory and Site Services - Lead (Study start up Lead)
United Kingdom,Belgium,Czech Republic,France,Germany,Hungary,Ireland,Italy,Netherlands,Poland,Portugal,Spain,Sweden
Apr 26
Working for Chiltern - home or office based - UK/EU
Regulatory Affairs Director
Surrey
Apr 26
We are currently seeking an experienced and highly motivated Regulatory Science Professional for the position of Director, Regulatory Science, Drugs & Biologics.The ability to lead by example in a positive environment is paramount in order to support our dynamic team. Our projects include the design and implementation of innovative drug/biologics development strategies and the preparation of regulatory submissions.
Teamlead Regulatory Affairs Medical Devices - Flache Hierarchien
Frankfurt am Main
Apr 25
Eine einmalige Gelegenheit Ihre Kompetenzen aus Regulatory Affairs und Qualitaetsmanagement in einem innovativen Unternehmen einzubringen und das Wachstum weiter auszubauen. Arbeiten bei einem dynamischen und...
Senior Regulatory Intelligence Manager - Surrey- £60,000-£70,000
England
Apr 25
Excellent opportunity for regulatory professional with expert knowledge in legislation for technical and regulatory aspects of ethical unlicensed medicines. Offering a consultative approach to pharmaceutical clients demands, identifying industry trends, providing regulatory processes from development through to launch including pricing and reimbursement processes.
Senior Associate Regulatory Affairs
Berkshire
Apr 25
Senior Associate Regulatory Affairs- CMCA fantastic opportunity for an experienced Regulatory Professional to join a global CRO. You will Prepare and review CMC regulatory submissions and have CMC responsibility for a portfolio of assigned products. ...
Regulatory Manager
Berkshire
Apr 25
Regulatory Affairs Manager - CMCA fantastic opportunity for an experienced Regulatory Professional to join a global CRO. You will Prepare and review CMC regulatory submissions and have CMC responsibility for a portfolio of assigned products. ...
Regulatory Manager
Italy
Apr 25
Regulatory Manager – Medical DeviceJOB SUMMARYExcellent opportunity for a Regulatory Professional with extensive Medical Device experience to join a cutting-edge company who specialise in the development of innovative products and procedures for Class III Medical Devices.Job TitleRegulatory Manager – Medical DeviceLocationNorthern East of ItalyBenefits – Above market salary, 15% Bonus, option to work 2 days from home a week, health insurance, pension. ...
Regulatory Manager
Italy
Apr 25
Regulatory Manager – Medical DeviceJOB SUMMARYExcellent opportunity for a Regulatory Professional with extensive Medical Device experience to join a cutting-edge company who specialise in the development of innovative products and procedures for Class III Medical Devices.Job TitleRegulatory Manager – Medical DeviceLocationNorthern East of ItalyBenefits – Above market salary, 15% Bonus, option to work 2 days from home a week, health insurance, pension. ...
Regulatory Submissions Coordinator - contract
Kent
Apr 25
Minimum 12 month contract for a regulatory affairs coordinator / regulatory submissions coordinator to join our client in Kent - competitive rate of pay available
Regulatory EMEA Director with a Global Top 20 Biotech company - Team leading role with opportunities to become a GRL
Brussels
Apr 25
This is a great role with a great company, offering excellent salaries and full re-location packages. The culture here is one of visibility and real product responsibility but with real regulatory support operational and strategic support available. Contact Theo Moore on +44 207 801 3384 or email your CV in confidence to CV@advregulatory.com
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OPTION BELGIQUE Director Regulatory Affairs Lead a Team 6 FTEs on new indication, market expansion, Biological Major Blockbuster
Brussels
Apr 25
You may be working as a matrix leader, or full direct manager, either in a CRO or within a pharmaceutical company. You may be working on a mix of products, and now want to focus and consolidate your lifecycle (including new indications) experience. You will be ready to embrace change and want to work in a leadership team which is visionary, has what it takes to turn the word innovation in to something a regulator will sign up to!
Regulatory Director and Associate Director Roles in Oncology (mAbs) – Become a GRL or Lead a Team - Salaries range from 100-165K Euros
Amsterdam and Leiden
Apr 25
They are seeking individuals who are ready or at Associate Director or Director level, want to work on both complex EU and / or global product development strategies in Oncology and want a career which can either encompass team management in time or GRL status - 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 / Global Regulatory Affairs strategy for early stage biological development projects / Brussels -
Brussels
Apr 25
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 Associate (1 year contract with possibility to extend)
Warsaw
Apr 25
PAREXEL Poland is looking for a clinical trial regulatory professional to join their Warsaw team.
Regulatory Affairs Director – EMEA strategy and Team Leading Role – Great Salary and Package - Brussels
Brussels
Apr 25
This role is a good mix of strategic input, global project management and covers early and late-phase development for a strong therapeutic franchise with a great mix of products. You will need enormous drive and enthusiasm, with the ability to inspire your team and the wider group to perform / achieve to a higher level. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
New Regulatory Affairs CMC Biologicals CONTRACT – Good rate – Flexible working hours – South-East
Maidenhead or Uxbridge
Apr 25
You will prepare, review and manage registrations and lifecycle activities for Biologicals in EU and International markets. It’s essential to have prior experience of working on Biologicals and ideally have hands-on experience of writing/authoring IMPD's. Call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Quality Assurance and Regulatory Officer, £30-40k, Medical Devices, South Wales
South Wales, Cardiff, Swansea, Newport, Hereford
Apr 25
This company are seeking a well organised, effective communicator to support the business in areas of Quality Assurance of Products and Services, meeting customers’ needs and achieving business results whilst ensuring Regulatory Compliance and driving excellence. The site is one of many across the UK and is part of a wider group, for which it acts as the flap ship for as it has been well established for over a decade.
Junior Regulatory Affairs Executive
United Kingdom Frimley / Camberley
Apr 25
Job Summary Do you want to work for a Global Generics company where you will get recognized for your hard work and commitment? Look no further, apply today. Sandoz is currently recruiting for an experienced Junior Regulatory Affairs Executive to join the team. Job purpose The purpose of the Junior Regulatory Affairs Executive role is to support the performance of pre and post approval regulatory activities to ensure compliance whilst supporting business needs. ...
Regulatory Affairs Executive
United Kingdom Frimley / Camberley
Apr 25
Job Summary Do you want to work for a Global Generics company where you will get recognized for your hard work and commitment? Look no further, apply today. Sandoz is currently recruiting for an experienced Regulatory Affairs Executive to join the team. Job purpose The purpose of the Regulatory Affairs Executive role is to perform pre and post approval regulatory activities to ensure compliance whilst supporting business needs. ...
Associate Director, Regulatory Affairs (Vaccines)-139817
Europe, Middle East and Africa-Belgium, Europe, Midd
Apr 25
Associate Director, Regulatory Affairs PPD Regulatory Affairs department has a new career opportunity available. The purpose of this role is to provide innovative solutions including global regulatory therapeutic area expertise and client interface to provide strategic regulatory intelligence, guidance and regulatory expertise for product development from preclinical through registration and product optimization. ...
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Regulatory Consultant-MDR Change Project-Medical Devices-Switzerland
Switzerland
Apr 24
After a recent partnership with a market leading Medical Device company I have been enlisted with an urgent contract for a regulatory affairs and quality assurance consultant. If you are available with short notice and have directly worked on the MDR changes, get in touch ASAP. You will play a crucial role within a leading medical device company to work on their gap analysis and lean improvement for the changes that are speculated around April time.
Global Regulatory CMC Expert - Biologics
Geneva
Apr 24
A renowned and world leading Pharma company with global reach are searching for a CMC expert. The CMC expert is in largely an operational role. This is a great opportunity for someone taking their first steps into Switzerland and would benefit a professional looking to make some positive changes to gain international experience working with one of the leading companies in the life science industry.
Regulatory Affairs Assistant - Essex
Essex
Apr 24
Oliver Care is recruiting for a Regulatory Affairs Assistant to join a company in the Chemical industry at their site based in Essex on a...
Manager, International Regulatory Affairs
Mahwah, New Jersey
Apr 24
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 Associate - Hertfordshire
Hertfordshire
Apr 24
Oliver Care is recruiting for a Regulatory Associate to join a company in the pharmaceutical industry at their site based in Hertfordshire on a 6...
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. ...
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 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 ...
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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. ...
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. ...
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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 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 ...
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.
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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. ...
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 ...
regulatory jobs : 100 +
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