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The latest Regulatory jobs

Jobs: (Regulatory)

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Associate Director Regulatory Affairs - Switzerland
Switzerland
May 25
I am interested to speak with highly experienced Regulatory Affairs professionals in the Biosimilars / Biologics field that are interested in working for a small biotech who are going through a very exciting period of growth! This position sits with a senior team where you will provide leadership on Biosimilar products.
Regulatory Affairs Professional- CMC
Vienna
May 25
ProClinical is working with a leading, niche, full-service global Regulatory Solutions and Services Company that supports Large, Medium and Small size global Life sciences companies in their entire Regulatory value-chain; ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions etc. This company is seeking a Regulatory Affairs Professional- CMC to be based in Vienna, Austria on a contract basis. ...
Regulatory Affairs Contract – 12months “Cover CTA’s, PiPs and Scientific Advice prep for EU development Projects”
South-East - M4 Corridor
May 25
We have a 12 month contract role for an expanding client in the M4 Corridor where you will be preparing scientific and regulatory documents for submission, providing input into development plans and creating regulatory strategy proposals. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com and call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Manager - consultant
Hertfordshire
May 25
Minimum 6-12 month contract for experienced senior reg affairs consultant / contractor offering competitive daily rate of pay. No line management required
Associate Director Regulatory Affairs - Switzerland
Switzerland
May 25
Plans and manages regulatory activities on new and in-line products.
Senior Regulatory Affairs Associate
Uxbridge
May 25
Our client is a pioneering company focused on combating heart disease and pushing the boundaries of science to transform medicine.
Regulatory Associate - Durham
Durham
May 25
Lucy Stendall is recruiting for a Regulatory Associate to join world leading science-led healthcare company at their site based in Durham, on a contract basis....
Regulatory Associate - Uxbridge
Uxbridge
May 25
Lucy Stendall is recruiting for a Regulatory Associate to join world leading science-led healthcare company at their site based in Uxbridge, West London, on a...
Regulatory Officer Submissions
Dublin, Republic of Ireland
May 24
Our client, a global pharmaceutical company, are currently recruiting for a Regulatory Officer Submissions. This is a 12 month contract role initially.
Regulatory Affairs Associate
Middlesex
May 24
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Affairs Associate on an initial 10 month contract to be based in their offices in Middlesex.
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Regulatory Affairs Labelling - Associate Director
Hertford
May 24
A leading pharmaceutical client is searching for an Regulatory Affairs Labelling - Associate Director to join their team in the UK. The company specialises in various therapy areas including oncology, neurology and gastroenterology, and employs several thousand across the globe. ...
Sr Manager Regulatory Affairs
Los Angeles
May 23
Sr. Manager, Regulatory Affairs SciPro Global are currently working with one of our key clients, a biopharmaceutical company who is actively engaged in the development of innovative cancer immunotherapies, based in California. Together, we are looking for a Manager/ Sr. Manager Regulatory Affairs to join their growing Regulatory Affairs team. As the Sr. ...
Regulatory Associate - Surrey
Surrey
May 23
Lucy Stendall at CK Group is recruiting for a Regulatory Associate to join a world leading pharmaceutical company at their site based in Surrey on...
Regulatory Affairs Director / Essex / Consultancy, Team Management, Strategy and `Hands-on` - Lead the Team
Essex
May 23
Director, Regulatory Affairs; Team management; Consulting; Client facing skills; full Regulatory Pipeline experience - Development, Registrations and Post marketing; Biologics and Pharma Product experience
Regulatory Affairs Assistant
England
May 23
This internationally recognised pharmaceutical organisation seeks a Regulatory Affairs Assistant to join their Medical Device sector.
Regulatory Affairs Specialist / RA Specialist / RA / Medical Devices / ISO 13485 / Surrey
Surrey
May 23
Job Title:  RA SpecialistSalary: CompetitiveLocation: SurreyI am currently working with a Medical Device company based in Surrey who are looking for an RA Specialist to join the team on a permanent basis.Interviews will be taking place starting next week so well worth a read.A great new opportunity has been created for an experienced Regulatory Affairs Specialist who will assist with the management of regulatory affairs and deputise for the Regulatory Affairs Manager, as necessary. ...
OPTION SUISSE Regulatory CMC Director Pure mAbs and Team Management role Development and Marketed, US and Europe and Int’l Majors
Switzerland
May 22
OPTION SUISSE ** Regulatory CMC Director *** Pure mAbs & Team Management role ** Development & Marketed, US and Europe & Int’l Majors? This role is based in Switzerland, within easy commute of Lausanne, Geneva, or Bern. The role comes with an advantageous package including RSUs.
Senior Specialist, Global Regulatory Affairs
Central London / West End
May 22
Regulatory Professionals are currently working with a long standing and established CRO with global a presence.
Senior Regulatory CMC Manager
Hertfordshire
May 22
Regulatory Professionals are working with a research based pharmaceutical company based in Hertfordshire.
Senior Regulatory Affairs Manager CMC
Cambridgeshire
May 22
Regulatory Professionals are working with a leading International pharmaceutical company who are looking for Senior Regulatory Manager CMC.
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Senior Regulatory Affairs Manager, CMC
Hertfordshire
May 22
Regulatory Professionals are working with a research based pharmaceutical company who works across the healthcare sector, aiming to discover and develop innovative medicines worldwide.
Regulatory Affairs Specialist - Medical Device - Home Based
Dublin
May 21
I am currently working with a Life Sciences Consultancy company who is looking for a Regulatory Affairs professional for a Medical Device end client.  The...
Regulatory Affairs Specialist - Medical Device
Home Based
May 21
I am currently working with a Life Sciences Consultancy company who is looking for a Regulatory Affairs professional for a Medical Device end client. The...
Regulatory Submissions Specialist/ Study Start Up
Belgium
May 21
REGULATORY SUBMISSIONS SPECIALIST/ STUDY START UP ASSOCIATE | BELGIUM | PERMANENT CONTRACT A client in Belgium is looking for a Submission Specialist or Study Start-up Associate to join their team in the Belgium.This international company is one of the top 10 in the whole market and is looking for ambitious candidates who are willing to join a new challenge for their career. ...
Regulatory Affairs Manager
Germany
May 21
Global Pharmaceutical company based near Frankfurt looking for a Regulatory Affairs Consultant for a 6 month period.
Regulatory Affairs Manager
Germany
May 21
This leading life science, health care and technology organisation seeks an experienced Regulatory Affairs Manager to join their established team.
Regulatory Affairs Manager- Medical Devices- Paris
France
May 21
Regulatory Affairs Manager- Medical Devices- Paris One of the most reputable Medical Device company is looking for experienced (4+ years) specialist with vast knowledge in Regulatory Affairs for Medical Device sector. If you'd like to join one of the most passionate teams in Paris, contact us today to find out more.
Senior Regulatory Affairs Officer
Warwickshire
May 21
Regulatory Professionals are working with an innovative medical device company specialising in medical imaging technology for cardiac activity.
Senior / Medical Writer, Regulatory (Home-based)-146315
Europe, Middle East and Africa-SA-Gauteng-Johannesbu
May 19
As part of our on-going growth, we are currently recruiting for a Senior / Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific. ...
Director Regulatory Affairs CMC - Biologics
Pennsylvania
May 18
Director Regulatory Affairs CMC – BiologicsEast CoastWorking together with one of our international clients, SciPro Global is actively searching for a Director Regulatory Affairs CMC Biologics to join a strong and established organization where you can provide your regulatory CMC expertise into in-licensing activities or new product development. ...
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Vice President, Regulatory Affairs – NA
Pennsylvania
May 18
Vice President, Regulatory Affairs – NAEast CoastWorking together with one of our international clients, SciPro Global is actively searching for a Vice President, Regulatory Affairs NA to join a strong and established organization to lead a great team of regulatory affairs professionals.My client, a pharmaceutical company based on the East Coast, is looking for someone who wants to join a strong international team to make a difference and change lives. ...
Regulatory Systems Analyst
Uxbridge
May 18
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory System Analyst- to be based at their offices in West London.
Regulatory Affairs Manager
Worthing
May 18
An exciting opportunity has arisen for a Regulatory Affairs Manager to join a Leading and Growing Speciality Immunotherapeutic Company. The position will lead the Regulatory function in the Registration and maintenance of company Vaccines across Europe and Internationally. This will report into the Head of Regulatory Affairs and may have line reports in UK and the EU. ...
Medical Devices - Regulatory Affairs (relocate to Stockholm)
Finland
May 18
Located in Finland but fluent in Swedish and open to relocate to Stockholm? If so, there an interesting opportunity at the moment with our global Medical Device client in their Stockholm office. Role would suite very experience candidate in Regulatory Affairs area with medical device products. ...
Regulatory Affairs Manager (m/w) in Hamburg
Hamburg
May 18
Regulatory Affairs Manager (m/w) in HAMBURG Sind Sie auf der Suche nach einer neuen, spannenden Herausforderung? Möchten Sie bei einem renommierten Pharmaunternehmen arbeiten? Suchen Sie nach interessanten Entwicklungsmöglichkeiten mit einem dynamischen und internationalen Team? Lesen Sie dann bitte weiter!Ihre Aufgaben: * Validierung elektronischer eCTD Zulassungsdokumentationen * Elektronische Archivierung länderspezifischer Unterlagen (Deutschland und Osteuropa) in einem Dokumentenmanagem ...
Associate Director, Regulatory Affairs - Netherlands
Leiden
May 18
Role Summary We are looking for an experienced Regulatory professional that wants to join a global pharmaceutical company and to act as an Associate Director of Regulatory. This individual will be responsible for managing regulatory strategy globally for a number of advanced therapies.
Executive Director Regulatory Affairs
Amsterdam
May 17
ProClinical is working with a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. This CRO is seeking an Executive Director Regulatory Affairs - Medical Devices to be based in the Netherlands on a permanent basis. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. ...
Regulatory Affairs Executive
Dublin, Republic of Ireland
May 17
Our client, a pharmaceutical drug discovery and development company, are currently recruiting for a Regulatory Affairs Executive. This is a permanent position within an exciting and innovative company.
Regulatory Affairs Manager
Dublin, Republic of Ireland
May 17
Our client, a pharmaceutical drug discovery and development company, are currently recruiting for a Regulatory Affairs Manager. This is a permanent position within an exciting and innovative company.
Associate Director Regulatory Affairs - Netherlands
Netherlands
May 17
Provides regulatory expertise for New Product Planning and Licensing due diligence activities. Manages the preparation and review of registration packages to ensure effective data presentation and quality scientific data against regulatory requirements. Interacts with FDA and global health authorities. Implements regulatory strategies and priorities, including original NDAs. 
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Senior Regulatory Affairs CMC Manager (m/w)
Frankfurt am Main
May 17
Position: Senior Regulatory Affairs CMC Manager (m/w)We are searching for a Senior Regulatory Affairs CMC Manager (m/w) for a fast-growing, successful and international leader in the pharmaceutical industry! An attractive salary, a very engaged, motivated and international team, as well as the opportunity to make a real difference in improving the lives of people await you!Location: Hessen, GermanyMain Responsibilities: * Provide strategic regulatory leadership and oversee all global CMC reg ...
Regulatory Affairs Director (Global Expansion Lead)
South East
May 17
A fantastic opportunity for a Global Regulatory Lead to join a well-established biopharmaceutical company as the Global Expansion Lead (Director). The GEL will be responsible...
Regulatory Consultant - Emerging Markets
Surrey
May 17
Here is an exciting pharmaceutical job one of the industry's most prestigious organisations. There is a vacancy for a Regulatory Consultant to join a global top 10 pharmaceutical company at their offices located in Surrey UK.Job Responsibilties: * Create and deliver strategic regulatory guidance for assigned projects/products, within Emerging Markets. ...
Senior Regulatory Affairs Associate – Global Markets – London
UK, Central London
May 17
My client is looking for an experienced regulatory affairs professional to join their established Regulatory team as a Senior Regulatory Affairs Associate in London. This role is perfect for ambitious people who want to grow their career with a highly reputable company.
Do you have five years regulatory CMC experience and want to lead a team of two International role
Midlands
May 17
To apply for this CMC Regulatory Affairs Manager please call Julie Cooper on 07951 082482 to discuss this role. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Global CMC Regulatory Affairs Manager - Midlands - will consider project manager level
Midlands
May 17
To apply for this CMC Regulatory Affairs Manager please call Julie Cooper on 07951 082482 to discuss this role. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Project Manager - Belgium
Belgium
May 17
This position develops and implements regulatory strategies and processes to assure timely global commercialization of CSS products in compliance with applicable European regulations and international standards. 
Associate Director Regulatory Labelling - Hertfordshire
Hertfordshire
May 17
Mary Bolt is recruiting for an Associate Director Regulatory Labelling to join a global pharmaceutical company committed to contributing to better healthcare at their site...
Associate Director, Regulatory Affairs, Marketed Products
London
May 17
A top 20 global biopharmaceutical company is looking to add a Regulatory Affairs Associate Director to their team in London to lead all regulatory work...
Regulatory Operations Manager
Sofia city
May 17
A Fantastic opportunity for a Regulatory Operations Manager to join a dynamic, fast growing Pharmaceutical Consultancy and work within the EU Regulatory team in managing...
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Regulatory Affairs Specialist/Senior Specialist
London
May 17
A growing company that specialises in Cosmetic Products in Central London is looking to add a Regulatory Affairs Specialist to their UK office to work...
Senior Regulatory Affairs Officer
West Midlands
May 17
Exclusive Regulatory Affairs Senior Officer job opportunity with a mid-sized, dynamic European medical device company to support the regulatory function in achieving regulatory compliance for...
Regulatory Affairs Consultant
London
May 17
This growing biopharmaceutical organisation seeks a Regulatory Consultant to join their team focusing on regulatory labelling on a short term contract basis.
Senior Regulatory Affairs Officer
South East
May 17
My client is a speciality pharmaceutical company who are looking to add a Regulatory Affairs Senior Officer to join the EU regulatory team. The Senior  ...
Regulatory Affairs Snr Manager - Join a dynamic Biotech with a great pipeline offering training to become a GRL - Brussels
Belgium
May 17
With their focus on natural, long-term growth, this amazing organisation depends on the contributions of talented and committed professionals like you who are determined to drive through progress. In turn, they make sure your work environment leaves you the space you need to attend to your personal goals, meet your family obligations, and pursue your professional development. Contact Theo Moore or Matt Greig NOW on +44 207 801 3384 or email us via CV@AdvRegualtory.com
Regulatory Affairs Director (Early Phase Global Development)
UK, M4 Corridor
May 17
You will work on US and EU as well as AP INDs, from regulatory strategy documents which you will co-author. The role is focused on early stage molecules, supporting 4 or so groups of indications, in a company where R&D is mostly based in Europe. A car allowance, bonus and stock plan are on offer for this role. 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.
Regulatory Policy and Intelligence Director UK W London or M4 OR 2/3 different EU locations
Multiple UK / EU Locations
May 17
NEW ROLE *** Regulatory Policy & Intelligence Director or Associate Director, Reg Policy & Intell We have 2 possibly 3 European locations open for this position, including the UK M4 Corridor area, and either French speaking, German or Dutch location. My client is a well-known, global, drug development company with a strong foothold in their chosen therapy areas and with a global objective ... >>> click to read on >>>
Regulatory Affairs Director - Lead Regulatory Policy for EMEA
UK, South-East
May 17
Would you consider a new opportunity if it gave you the chance to drive and shape policy across the entire development portfolio of Biologicals in a highly visible and influential role? This is highly visible and influential role, which would suit someone looking for a big challenge with a quickly developing and growing organisation. 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.
Sr. Manager, Regulatory Writing
Los Angeles Metro Area
May 16
The Senior Manager, Regulatory Writing will report to the Director of Regulatory Writing. The regulatory writer will be responsible for writing and/or editing clinical documents for INDs, BLAs, MAAs, and associated regulatory submissions. ...
QARA Officer / Quality / Regulatory Officer / Medical Devices / ISO 13485 / Essex
Essex
May 16
Job Title: QARA OfficerSalary: £25,000 - £35,000Location: EssexA brand new position has just opened up with a Medical Devices company based in Essex.They are looking for someone with 2 – 3 years’ experience in Quality Assurance and Regulatory Affairs within the Medical Devices industry.The position will enable the QARA Officer to develop and expand their Quality and Regulatory experience within a dynamic team that is constantly looking to expand and grow as the company grows. ...
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Regulatory Affairs Manager in Norddeutschland gesucht (m/w)
Hamburg
May 16
Regulatory Affairs Manager in Norddeutschland gesucht (m/w)Office-based in Hamburg Mein Kunde, ein hoch innovatives weltweit agierendes Unternehmen, das Weltmarktführer seiner Produktsparte ist, sucht kluge Köpfe, die Lust haben sich neuen Herausforderungen zu stellen. ...
Freelance Regulatory Consultant - Clinical Trial Focussed
Europe, Home Based
May 16
**URGENT ** FREELANCE ** REGULATORY AFFAIRS ** CLINICAL TRIALS ** EUDRACT **
Regulatory Affairs Specialist - Danderyd
Sweden
May 16
Din nya rollDu kommer som huvudsaklig uppgift att ansvara för regulatoriska ansökningar främst inom Europa och Kanada men naturligtvis stödja alla typer av internationella ansökningar. Du kommer att ha ett tätt samarbete med hela organisation dock främst utvecklings- och marknadsavdelningen. ...
Pre-Clinical Regulatory Consultant - Freelance
Home Based, Europe
May 16
**URGENT ** FREELANCE ** MODULE 2.4/2.6 ** REGULATORY CONSULTANT **PRE-CLINICAL **
Regulatory Affairs Senior Officer
Belgium
May 16
An exciting opportunity has arisen to join this medium sized global company and manage their regulatory activities. In the function of Regulatory-Affairs Officer you are responsible for writing scientific documents, regulatory reports and managing the lifecycle of the drug from preparation, submission and launch of the registered drug.
Senior Regulatory Officer / Regulatory Affairs
Wiltshire
May 16
Theyre expanding the Regulatory Affairs department and are looking to bring on a new Regulatory CMC professional who will keep member of the team.
Regulatory Affairs RIMS Specialist
Germany
May 16
Zur Zeit suche ich nach Regulatory Affairs RIMS Spezialisten in Hessen. Ein internationaler Biopharma Unternehmen braucht Unterstützung beim eCTD, NeeS und XEVMPD Aktivitäten. ...
Regulatory Start Up Manager (Spain)
England
May 16
Premier Research helps highly innovative biopharmaceutical and medical device companies transform life-changing ideas into reality. We take on the most challenging areas of study, with a special focus on unmet needs in such areas as analgesia, CNS, rare diseases, medical device and diagnostics, and pediatric research.
Regulatory affairs - Submissions Expert
Paris
May 16
ProClinical is working with a specialty pharma that is seeking a Regulatory Affairs Submissions Expert to be based in Paris on a contract basis. This RA Submissions Expert role will ensure regulatory compliance on a portfolio of approximately 125 licences. ...
Senior Regulatory Affairs Manager - Biotech
Amsterdam
May 16
ProClinical is seeking a Senior Regulatory Affairs Manager for a global biotech leader. This role is a 3-6-month contract and will be based in Amsterdam.Job Responsibilties: * Lead regulatory strategy and operational implementation of development programs * Prepare and compile the Common Technical Document (CTD) for dossier submission according to regulatory requirements of different regions (e.g. ...
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Regulatory CMC Lead
Amsterdam
May 16
An excellent regulatory affairs job opportunity has arisen for a Regulatory CMC Lead to work with a leading global contract research organisation at the forefront of drug development. The company boast an excellent working environment, challenging training and development programmes and exciting projects to work on. ...
Regulatory Labelling Manager
Amsterdam
May 16
A well-known international pharmaceutical company with sites around the globe is looking to hire a Regulatory Labelling Manager to be based in Netherlands. The company specialises in developing and producing medicines and vaccines for a wide range of therapeutic areas including oncology, cardiology and immunology. ...
Team Director Regulatory CMC Biologicals (mAbs) Based in 1 of 3 UK or EU Locations Big team, decent pipeline, great people
UK, CH or Europe
May 16
You will have a strong track record in regulatory strategy leadership for CMC for biologicals and some team management either full line or fuller matrix, and want to take on more of a people leadership role, in a company where behaviours and success factors, are important mantras in management roles.
UK Regulatory Affairs Manager
Hertfordshire
May 16
Exciting full-time permanent opportunity for an experienced regulatory professional with post-marketing lifecycle experience to join our client - competitive package available
Regulatory Affairs Assistant (f/m)
Germany Munich 80636
May 16
Regulatory Affairs Assistant (f/m) - Munich Office-based   Who We Are Synteract is a global full-service contract research organization with a successful three-decade track record supporting biotechnology, medical device and pharmaceutical companies. With our mission of ”Bringing Clinical Trials to Life,” we provide customized Phase I through IV services internationally, offering expertise across multiple therapeutic areas including notable depth in Oncology, Neuro Degenerative...
Quality and Regulatory Affairs Manager, Medizintechnik
Stuttgart
May 16
Quality and Regulatory Affairs Manager – innovativer Medizintechnikhersteller, Stuttgart Sie haben bereits Erfahrung im Bereich Qualitätsmanagement und Compliance in der Medizintechnik? Sie fühlen sich in einem regulierten Umfeld wohl? Sie arbeiten gern in einem kollegialen Team? Wenn ja, dann ist die Position genau das Richtige für Sie! Unternehmen:Das Unternehmen gehört zu den weltweit führenden Herstellern in der Medizintechnikbranche. ...
Regulatory Affairs Manager (m/f)
Darmstadt,Germany
May 15
For one of the most successful global players in the pharmaceutical industry DOCS is hiring a Senior Regulatory Affairs Manager (m/f). If you like to challenge yourself with interim projects in the area of regulatory affairs or you are looking to get a foot in the door of one of the top players in the pharmaceutical industry, than this might be for you. The successful candidate will support the national RA team in Germany working on/with text variations, MRP’s,...
Regulatory Officer Compliance
Dublin, Republic of Ireland
May 15
Our client, a global pharmaceutical company,  are currently recruiting for a Regulatory Officer Compliance. This is a 12 month contract role initially.
Regulatory Affairs Project Officer
Belgium
May 15
An exciting opportunity has arisen to join this medium sized global company and manage their regulatory activities. In the function of Regulatory-Affairs Officer you are responsible for writing scientific documents, regulatory reports and managing the lifecycle of the drug from preparation, submission and launch of the registered drug.
Regulatory Affairs Spezialist für Software Produkte gesucht
Switzerland
May 15
Regulatory Affairs Spezialist für Software Produkte gesucht!Office-based in der Schweiz Sie legen besonderen Wert auf eine gute Arbeitsatmosphäre und einen tollen Team Spirit?Sie bilden sich gerne weiter und lieben die Herausforderung?Sie möchten Teil eines hoch innovativen und stark wachsenden Unternehmens sein? Dann nutzen Sie Ihre Chance jetzt! Alles was Sie brauchen: * Ein technisches Studium * 1 Jahr Berufserfahrung in der Medizintechnik- Branche * Kenntnisse im Qualitätsmanagement nach ...
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Regulatory Affairs Manager - UK
Glasgow
May 15
Clintec are actively recruiting for a Regulatory Affairs Manager to join our team here in the UK. The successful candidate would ideally be working office based from our Glasgow HQ however we may also consider candidates working from home based or partially home based elsewhere in the UK
Regulatory Affairs Officer
Edinburgh
May 15
My Client a Global Healthcare company has opened a new vacancy within their Regulatory Affairs team. They are actively seeking to recruit a Regulatory Affairs Officer to work at their offices in the Scotland.
Regulatory Affairs Manager
Edinburgh
May 15
My Client a Global Healthcare company has opened a new vacancy within their Regulatory Affairs team. They are actively seeking to recruit a Regulatory Affairs Manager to work at their offices in the Scotland.
Regulatory Project Manager
Belgium
May 15
Based in the European HQ in Belgium, the Regulatory Project Manager reports to the Director, Regulatory Affairs, Global & EU. This position develops and implements regulatory strategies and processes to assure timely global commercialization of CSS products in compliance with applicable European regulations and international standards.
Study Start up / Regulatory Affairs
Munich, Germany
May 15
If you are interested in learning more, please get in touch
AD Regulatory Labeling
Massachusetts
May 15
My client is an exciting biotech company who have one of the most exciting pipeline's in the Boston Hub. This is a pivotal role within the organization as they are looking to file their first BLA in Q3/Q4 and this person will be responsible for all labeling activities.
Regulatory Officer (Home Based) 6 Month Contract (Urgent)
Home Based
May 15
One of our top clients is actively searching for a Home based Regulatory Affairs contractor to join the company for a 6-month period (with potential to be extended to a permanent position) and to work from home for this period. This fantastic global Clinical Research Organisation are at the forefront of the clinical market and are looking to expand their Regulatory Team long term. 
Regulatory Operations Specialist DACH
Germany
May 15
Aktuell suchen wir nach einen Regulatory Operations Spezialisten für die DACH Region.Sie werden verantwortlich für die Erstellung und Betreung von eCTD, Nees, XEVMPD und IDMP sein. ...
Regulatory Operations Manager (m/w) in Frankfurt
Frankfurt am Main
May 15
Regulatory Operations Manager (m/w) in FRANKFURTHaben Sie schon Erfahrung im Bereich Regulatory Operations gesammelt? Sind Sie auf der Suche nach einer neuen, spannenden Position? Möchten Sie bei einem renommierten Pharmaunternehmen mit innovativen biopharmazeutischen Produkten arbeiten? Suchen Sie nach interessanten Entwicklungsmöglichkeiten mit einem dynamischen und internationalen Team? Lesen Sie dann bitte weiter!Ihre Aufgaben: * Validierung elektronischer eCTD Zulassungsdokumentationen ...
Quality and Regulatory Affairs Managerr, Medizintechnik
Stuttgart
May 14
Quality and Regulatory Affairs Manager – innovativer Medizintechnikhersteller, Stuttgart Sie haben bereits Erfahrung im Bereich Qualitätsmanagement und Compliance in der Medizintechnik? Sie fühlen sich in einem regulierten Umfeld wohl? Sie arbeiten gern in einem kollegialen Team? Wenn ja, dann ist die Position genau das Richtige für Sie! Unternehmen:Das Unternehmen gehört zu den weltweit führenden Herstellern in der Medizintechnikbranche. ...
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Regulatory Affairs Manager - Surrey
Surrey
May 14
Mary Bolt is recruiting for a Regulatory Affairs Manager to join a global biopharmaceutical company that strive to enhance lives and quality of life at...
EMEA Regulatory Affairs Manager - Oncology - High Wycombe
High Wycombe
May 14
Mary Bolt is recruiting for an EMEA Regulatory Affairs Manager - Oncology to join a highly established research-based pharmaceutical company with a mission to change the...
EMEA Regulatory Affairs Manager - High Wycombe
High Wycombe
May 14
Mary Bolt is recruiting for an EMEA Regulatory Affairs Manager to join a highly established research-based pharmaceutical company with a mission to change the way...
Senior Regulatory Project Manager - High Wycombe
High Wycombe
May 14
Mary Bolt is recruiting for a Senior Regulatory Project Manager to join a highly established research-based pharmaceutical company at their site based in High Wycombe...
Regulatory Affairs Manager (m/w) EU
Berlin
May 14
Regulatory Affairs Manager (m/w) EUBerlin, Deutschland / office-based, Vollzeit Aufgaben:- Das Erlangen und die Aufrechterhaltung von Zulassungen in Europa, inklusive das Management aller Aktivitäten Rund um der Enreichung und Behördenkommunikation- Das Erstellen aller relevanter Zulassungsdokumentationen, sowie deren Einreichung und das Management der Submissions Tracking Applikationen- Die Überwachung des regulatorischen Umfeldsum sicher zu stellen, dass alle relevanten Änderungen umgesetz ...
Regulatory Manager
Bedford
May 14
Regulatory Professionals are currently working with an innovative Global Biopharmaceutical Company whose focus is to deliver life changing medicines, push boundaries and ways of thinking.
Regulatory Affairs Manager UKandI
Surrey
May 14
Exciting full-time permanent opportunity for an experienced regulatory professional to join our client as Reg Affairs Manager for UK & Ireland - highly competitive package available
Regulatory Operations Switzerland
Switzerland
May 14
Der Regulatory Operations Market in der DACH Region ist stark am wachsen. Vor kurzem haben wir zwei Projekte in Deutschland besetzen können. Ein projekt in Deutschland ist noch aktiv und jetzt bieten wir auch eine Stelle in der Schweiz. Aktuell suchen wir nach Reg Ops Spezialisten in der Schweiz. Unser Auftraggeber ist ein internationaler Biopharma Unternehmen das Unterstützung im eCTD, NeeS und XEVMPD Bereichen braucht. Die Stelle ist Office Based mit 1 FTE zu besetzen. ...
LOCAL REGULATORY AFFAIRS LEAD - United Kingdom
Reading, United Kingdom
May 14
At PRA we know our greatest strength is our people. We have a commitment to employee development and a culture that values innovation. Where great minds work everything is possible.
Regulatory Affairs Consultant (m/f) 4 Month Contract
Germany
May 14
Regulatory Affairs Consultant (m/f) Freelance 4 Months Project Role: - Developing and driving global regulatory aspects for all types of drugs. - Post-market applications of existing products. - Providing advice and assistance to clients in all regulatory matters - Authorship of regulatory key documents. Requirements: - Degree in pharmacy, biology, biotechnology or equivalent in other Life Sciences. ...
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The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.