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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Associate Director, Regulatory Labeling (CCDS) - Salary to $185,000 + Bonus / LTI - Northbrook, Illinois
Northbrook, Illinois
May 30
We invite you to apply, please contact, Matt Greig, at Advanced Regulatory, on 855-505-1382 (Toll Free). Alternatively, send a full CV quoting reference STAR1505/01 to Star@AdvRegulatory.com and we will be in touch directly.
Associate Director, Regulatory Labeling (CCDS) - Salary to $185,000 + Bonus / LTI - Northbrook, Illinois
Northbrook, Illinois
May 30
We invite you to apply, please contact, Matt Greig, at Advanced Regulatory, on 855-505-1382 (Toll Free). Alternatively, send a full CV quoting reference STAR1505/01 to Star@AdvRegulatory.com and we will be in touch directly.
Director, Regulatory Advertising/Promotion - Salary to $220,000 + Bonus / LTI - Northbrook, Illinois
Northbrook, Illinois
May 30
We invite you to apply, please contact, Matt Greig, at Advanced Regulatory, on 855-505-1382 (Toll Free). Alternatively, send a full CV quoting reference STAR1505/02 to Star@AdvRegulatory.com and we will be in touch directly.
Regulatory Director - Latin America - Salary to $220,000 + Bonus / LTI - Northbrook, Illinois
Northbrook, Illinois
May 30
We invite you to apply, please contact, Matt Greig, at Advanced Regulatory, on 855-505-1382 (Toll Free). Alternatively, send a full CV quoting reference STAR1505/03 to Star@AdvRegulatory.com and we will be in touch directly.
Senior Manager, Regulatory Affairs - Inhalation Products
Germany
May 29
SEC has been enlisted to assist the Centre of Excellence of a global pharma group in their search for two experienced regulatory professionals to join their Development Regulatory Team. This particular client site is “ground zero” for the manufacturing of respiratory and ophthalmic products. ...
Solutions Engineer (Life Sciences), Regulatory and Medical
Buckinghamshire
May 29
As one of the preferred recruitment partners, SEC Pharma is collaborating with a growing international life sciences product development company in recruiting for a “Solutions Engineer” for their Regulatory and Medical Affairs product development/services areas. ...
Regulatory Affairs Manager
Maidenhead
May 29
An internationally known biotechnology company situated in Maidenhead and operating in over 70 markets worldwide is looking for a Regulatory Affairs Manager. The company specialises in neurological conditions and puts a great emphasis on team work and delivering biological products. This is a 9 month contract role with the possibility of an extension. ...
Senior Regulatory Associate - 12 month contract (Development)
West London
May 29
We are currently assisting a large pharmaceutical company with the search for a Senior Regulatory Associate to join their team on a 12 month contract basis. This vacancy has become available due to recent expansion within the team. The ideal candidate will have 1-3 years of Regulatory experience and have a solid understanding of the drug development process.
Senior Regulatory Consultant
London
May 29
An internationally known pharmaceutical company situated in London and operating in over 150 markets worldwide is looking to hire a Senior Regulatory Consultant. The company develops a broad range of products in pharmaceuticals, vaccines and consumer healthcare. This is a 6 month contract role with the possibility of an extension. ...
Head of Quality Management and Regulatory Affairs (m/w)
Bavaria
May 29
Head of Quality Management and Regulatory Affairs (m/w) Im Raum München, DeutschlandIhre Aufgabe• weltweite Verantwortung für alle qualitätsrelevanten Themen• Aufrechterhalten und Weiterentwicklung des QM-System nach den Anforderungen der MDD, ISO 13485:2003, cGMP und 21 CFR 803, 806, 820• Überwachung und Optimierung von Prozessen und Dokumentationen• Unterstützung der Geschäftsführung durch ein aktives Risikomanagement• Vorbereitung und Durchführung regelmäßiger Management-Reviews• Schnitt ...
Regulatory Affair Specialist
West London
May 29
I am currently representing a medium sized life sciences company based in West London.
Medical Device Regulatory Manager (m/w) Freelance
Bavaria
May 29
Medical Device Regulatory Manager (m/w) FreelanceVZ, ½ Jahr – 8 Monate Im Raum München, DeutschlandIhre Aufgabe• Normprotokolle neu erstellen• Risiko Analysen nach ISO 14971 durchführen• Erfahrung mit Klasse IIa/b Medizinprodukten• Produktzulassungen auf internationaler und nationaler Ebene• Erstellen aller nötigen Dokumente für die internationale Registrierung • Direkter Ansprechpartner für Behörden und Ämter• Interne und externe Anfragenbearbeitung der RA RichtlinienIhre Qualifikation• Erf ...
SSU and Regulatory Specialist II - Israel (temporary)
Tel Aviv, Israel
May 29
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.
Astellas - Associate Director, Regulatory Labeling (CCDS)
Northbrook, Illinois
May 29
Astellas is an organization where our people matter, individuals empower and support each other, for the peaks in our work-streams, peer review and to support cross-functional working and initiatives. If you are based in North America and want to apply, please contact, Matt Grieg, at Advanced Regulatory, on 855-505-1382 & If you are based in the EU and wish to apply, please contact Theo Moore in the UK London office, on +44 (0)207 801 338
Astellas - Director, Regulatory Advertising/Promotion
Northbrook, Illinois
May 29
This is a highly visible and rewarding position for a credible, talented individual with the depth and breadth of US Advertising and Promotion experience. If you wish to apply for this role please contact, Matt Grieg, at Advanced Regulatory, on 855-505-1382 or for EU based candidates send your CV to CV@AdvRegulatory.com or call Theo Moore on +44 (0)207 801 3380
Astellas - Regulatory Director, Latin America
Northbrook, Illinois
May 29
Astellas is an organization where our people matter, individuals empower and support each other, for the peaks in our workstreams, peer review and to support cross-functional working and initiatives. If you wish to apply for this role send your CV to Star@AdvRegulatory.com and we will be in touch directly.
Regulatory Affairs Consultant (Medical Devices)
Yorkshire and the Humber
May 29
Are you looking for a short-medium term Regulatory Affairs Contract that can be done from home?*EXPERIENCE IN MEDICAL DEVICES ESSENTIAL* An exciting, growing international Medical Device company is currently seeking a Regulatory Affairs Consultant for a couple of short term projects which can be done from home if required.
Drug Regulatory Affairs Manager (m/w)
Basel-City
May 29
Regulatory Affairs CMC Manager (m/w)Office-based in der Nähe von BaselAufgaben:? Kontakt zu Behörden in der EU, CH, JP und den USA, sowie z.B Scientific Advice und Pre-submission Meetings? Erstellung und Pflege der relevanten Zulassungsdossiers und Zulassungen, sowie Scientific Advice requests, IMPDS/INDs, MAAs/ANDAs, Lifecycle Managment- und Maintenance-Aktivitäten? Überprüfung und Erstellung der CTD Module 1-5, insbesondere die CMC/Qualitätsdokumentation (QOS Modul 2. ...
Senior Regulatory Affairs Manager (m/w)
Munich
May 29
Senior Regulatory Affairs Manager (m/w)Office-based in MünchenAufgaben:? Sie beurteilen Zulassungsprojekte? Sie planen, koordinieren und führen nationale sowie auf EU Ebene befindliche Zulassungsverfahren (DCP, MRP) und Variations durch? Sie übernehmen die regulatorische Betreuung bestehender Zulassungen, auch im Kontakt mit anderen Abteilungen des Geschäftsbereiches)? Sie erstellen und aktualisieren chemisch-pharmazeutische Dossiers? Sie arbeiten eng mit Behörden und unseren industriellen K ...
Regulatory Affairs Associate – Labeling – Ulm
Ulm
May 29
Als Regulatory Affairs Associate arbeiten Sie an verschiedenen Projekten im Bereich Regulatory Affairs. Ein besonderer Schwerpunkt wird auf der Erstellung von Produktinformationen und andere Aufgaben im Bereich Labeling liegen. Ein anderer Schwerpunkt Ihrer Arbeit liegt in der Kommunikation mit verschiedenen Kunden und Repräsentation des Unternehmens. Sie werden Ihre Tätigkeiten mit anderen Mitarbeitern in der Zulassung sowie anderen Abteilungen koordinieren.
Contract Junior Regulatory Affairs Specialist
Leeds
May 29
Contract Junior Regulatory Affairs Specialist Our client, a globally recognised Healthcare company, have an opportunity for a Junior Regulatory Affairs Specialist to join their team in Leeds. Offering a fantastic working environment and the opportunity to work for a company which is internationally recognised, we are looking for someone who has good regulatory affairs experience with technical files and design dossiers. ...
Regulatory Affairs Manager (Medical Devices)
Gloucestershire
May 29
*EXPERIENCE IN MEDICAL DEVICES ESSENTIAL* An exciting, growing international Medical Device company is currently seeking a Regulatory Affairs Manager focused on QMS and Technical files.The Regulatory Affairs Manager will be responsible for ensuring compliance with all medical device standards for the QMS, Leading the maintenance of technical files, design dossiers and device master records, maintenance and continuous improvement of the established QMS.
EXCLUSIVE REGULATORY AFFAIRS MANAGER
England
May 29
One of the most innovative and fastest growing consumer healthcare companies in the UK/IE has an opportunity for a talented Global Regulatory Affairs Director to join their team based in London, in order to complete regulatory leadership across assigned categories e.g. Urologicals, Pain. Team Mission: To be a world class regulatory function which everyone wants to join and no-one wants to leave.
Regulatory Submissions Specialist
Basel, Switzerland
May 28
Our client is a leading biopharmaceutical company with more than 30 operating affiliates worldwide. With 5 products on the market and a rich pipeline, the company continuously invests in innovation and growth.
Global Regulatory Affairs – High Risk – Near Frankfurt
Frankfurt am Main
May 28
Global Regulatory AffairsHigh Risk Product - Class IIIFuture Forward MarketManagement Position
Senior Regulatory Manager (m/w) der Medizintechnik Freelance
Bavaria
May 28
Senior Regulatory Manager (m/w) der MedizintechnikFreelance3-4 Tage Auslastung, 7 Monate mit späterer 90%iger Home-Office OptionIm Raum München, DeutschlandIhre Aufgabe• Erfahrung mit Drug/ Device Products (nice to have)• Erfahrung mit CE Zertifizierung (must have)• Erfahrung mit 510 (k) Zertifizierung (must have)• Erfahrung mit aktiven Medizinprodukten (must have)• Erfahrung mit Sterilisations- und Biocomp. ...
EXCLUSIVE REGULATORY AFFAIRS DIRECTOR
France
May 28
One of the most innovative and fastest growing consumer healthcare companies in the UK/IE has an opportunity for a talented Global Regulatory Affairs Director to join their team based in London, in order to complete regulatory leadership across assigned categories e.g. Urologicals, Pain.
Senior Regulatory Affairs Manager – UK / Ire Markets – London
UK, London
May 28
My client is looking for an experienced regulatory affairs professional to join their established Regulatory team as a Senior Regulatory Affairs Manager in London. This role is perfect for ambitious people who want to grow their career with a highly reputable company. Get in touch with Nick@peoplewithchemistry.com for more details
Regulatory Affairs Coordinator, Asia-Pacific
Amsterdam, The Netherlands
May 28
My client is a dynamic and expanding specialist biopharmaceutical company; a patient focused organisation that strives for innovation to develop medicines to address areas of unmet medical need. The high performing and talented regulatory team in the Netherlands is currently offering an opportunity for an experienced Regulatory Affairs Coordinator to project manage Asia-Pacific submissions on a permanent basis.
EMEA Regulatory Affairs Director – UK
United Kingdom
May 28
I am currently partnering with a smaller sized, extremely innovative, global pharmaceutical company on an Executive Search assignment to appoint the right individual into a senior level position within Regulatory Affairs.
Senior Regulatory Affairs Officer - Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
May 28
To apply for this regulatory affairs project manager role you will need to either call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Head of Regulatory Operations
Germany
May 28
An excellent opportunity has arisen to join one a leading pharmaceutical company based Germany. They are looking for an experienced regulatory professional for the position of Head of Regulatory Operations - based in Germany.
Regulatory Affairs Manager - Biocides - Hamburg
Hamburg
May 28
I am currently searching for a Regulatory Affairs manager for Biocidal products for one of my clients based in Hamburg, Germany. This is the perfect opportunity for someone that would like to work in a friendly and supportive environment with lots of training opportunities!Int his role you will be responsible for all regulatory supervision of international development projects for biocides and related product categories. ...
Regulatory Writer- State of the Art Facilities – Cambridgeshire
Cambridge
May 28
My client is looking for a Senior Regulatory Writer to join their Leading Pharmaceutical Company in their new state of the art facilities. You will have access to some of the best resources. Due to the size of this company you will have chance to liaise with a wide range of different teams across the globe. As a result of the size of this company you there are clear paths of progression mapped out, so you won’t be stuck beneath a glass ceiling. ...
Regulatory Affairs Document Controller
Cambridgeshire
May 28
We have a new and exciting pharmaceutical career opportunity for a Regulatory Affairs Document Controller to work within a rapidly expanding pharma company that specialises in the research and development of treatments for areas that have unmet medical need. This job will be based at their UK site in Cambridgeshire. Role: For this Regulatory Affairs Document Controller job you will be working with other Document Coordinators to manage the documentation required for regulatory submissions. ...
Regulatory Officer, CMC, Belgium
Ghent, Belgium
May 28
My client is an expanding and dynamic consultancy offering specialist regulatory consultancy services to Pharma and Biotech industries. As a result of business growth through the company’s excellent reputation, there is a need for a regulatory professional on a permanent basis close to Ghent in Belgium. In return the Regulatory Officer can look forward to a challenging and varied technical position.
Regulatory Project Manager
Belgium
May 28
Oliver Care at CK Clinical is recruiting for a Regulatory Project Manager to join a company in the pharmaceutical industry at their site based in...
Regulatory Affairs Specialist
Leeds
May 28
Oliver Care at CK Clinical is recruiting for a Regulatory Affairs Specialist to join a company in the Pharmaceutical industry at their site based in...
Regulatory Specialist-Leading Medical Technology Company-BE
Brussels
May 28
Regulatory Specialist-Leading Medical Technology Company-BEMy client, a leading medical technology company in Belgium is looking for a Regulatory Affairs Specialist to join their European Regulatory team. With operations across 50 countries globally and a company ethos of promotion within, you will take the steps to learn, develop and further your career in a supportive environment, whilst gaining huge visibility within a growing market area.
Global Regulatory Strategist
New Jersey
May 27
This position is with a global pharmaceutical company and gives the incumbent the opportunity to lead a team with Global Medical Device Regulatory Strategy. The...
Regulatory Affairs CMC Assistant Contract
North West England
May 27
My client, a global Pharmaceutical company are searching for a Regulatory Affairs CMC Assistant to join them in their office based in the North West of England. The role is a contract and is running for a 6 month period, with the potential for a further 6 month extension. My client is offering a competitive salary for this role and is looking for someone to start ASAP.
Regulatory Affairs Associate – Growing Company – Belgium
Belgium
May 27
Do you want to work for a global pharmaceutical company? Do you like to be involved in the regulations of a big product portfolio? Career progression? Then this opportunity gives you the perfect combination. The company is looking for a regulatory affairs associate responsible for the generic product portfolio. Because they are growing globally you can grow within this company and take on more responsibilities.
Regulatory Affairs Manager – Cross-Functional Role – Belgium
Belgium
May 27
A pharmaceutical company is looking for a regulatory affairs manager who will be responsible for the regulatory affairs team and a big portfolio of generic products. You will have contact with other departments so also coordinate their activities which will give you a lot of variety in the job.
Regulatory Affairs Specialist
Switzerland
May 27
Global medical devices company with their headquarters in Switzerland is looking for a Regulatory Affairs Specialist to join their team to help support daily activities for maintenance of technical files. This is 6 months contract based on site in Switzerland to start ASAP.Role: This Regulatory Affairs Specialist job will have some key accountabilities that include: - Reviewing of Risk Management Documentation according to EN ISO 14971:2012 with respect to regulatory requirements. ...
Interim – Regulatory Affairs Manager
Amsterdam
May 27
My client a world leader in the Pharmaceutical sector is looking for an all-around experience regulatory affairs manager to join their division. This would be an excellent opportunity for you to get into one of Europe's top employers and work for a company which operates in more than 140 countries across the globe. This position would require you to work 4 days a week offering you flexibility and work life-balance.
Regulatory Executive – Labelling
Middlesex
May 27
Great new opportunity available for a Regulatory Associate to join an expanding team within a global pharma. Please contact me for more details!
Head of Regulatory Affairs UK and Ireland
England
May 27
*** Permanent position *** Head of Regulatory Affairs UK & Ireland. Competitive salary offered!
Regulatory Affairs Specialist
Dublin
May 27
A leading consultancy with an international client portfolio is currently recruiting for a Regulatory Affairs Specialist to join its growing Regulatory Affairs technical team specialising in chemicals. The company’s industry sectors are diverse and include pharmaceuticals, fine chemicals, cosmetics, IT, medical devices, mining and food.As a Regulatory Affairs Specialist, you will support the development and delivery of a variety of Regulatory and technical programmes that are assigned. ...
Senior Regulatory Affairs Associate - LATAM role
Cambridge
May 27
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Executive Senior
Middlesex
May 27
Oliver Care at CK Clinical is recruiting for a Regulatory Executive Senior to join a company in the Pharmaceutical industry at their site based in...
Senior Regulatory Affairs Officer
Kent
May 27
Senior Regulatory Affairs Officer. Our client is a globally recognised company specialising in IVD’s and medical devices operating in over 50 countries worldwide. They are a recognised investor in people and take pride in advancing careers. We are looking for a standalone self-initiated professional who is looking to expand their knowledge within a globally focussed role.
Regulatory Affairs Associate (m/w)
Frankfurt am Main
May 27
Regulatory Affairs Associate (m/w)Office-based near BerlinJob Description:? Formal review of the content of regulatory documents for plausibility and suitability for submissions? Managing the publishing software and creating eSubmissions? Maintaining the database and coding of information? Preparation and support the implementation of submissions and registration procedures and submit notifications of changesRequirements:? Life science training or relevant degree? 2 years of experience in th ...
Freelance Study Start-up Specialist – Regulatory, Growing CRO, Ethics, Submissions – CZECH REP
Prague office, Czech Rep - some home working
May 27
New opening has arisen to join one of the worlds leading mid-size CROs, looking to add a talented, ambitious Regulatory Start-up Specialist to their Czech Republic division. Working office based in Prague (50% of time minimum) this position will see you working across the full range of study start-up activities from ethics & regulatory submissions for local committees and health authorities, working closely with clinical teams. 3 – 6 month initial contract paying a competitive hourly rate.
Regulatory Affairs Manager
Germany
May 27
Regulatory Affairs Manager. Standort: Hamburg, Germany Haben Sie eine Interesse in den Regulatory Affairs und eine Höhe Affinität zur asiatischen Kulturen? Mein Klient ist einer maßgebenden Hersteller von innovativen optischen und digitalen Ausrüstung für die Bereiche Gesundheitswesen und Consumer-Elektronik. Er sucht nach eine begeisterte Person mit ausgezeichneten kommunikativen Fähigkeiten und Aufmerksamkeit zum Detail in den Regulatory Affairs.
Regulatory Affairs Officer - Dublin
Dublin
May 27
Regulatory Affairs Officer Location: Dublin. Salary: €39,000 + Great Benefits. An amazing opportunity has arisen to become part of one of the largest generics company in the world. The position will benefit anyone who is looking to broaden their experience within Regulatory Affairs as well as offer successful candidates the opportunity to work across a wide range of therapy areas in a fast paced, structured environment.
Regulatory Affairs Specialist, Galway
GALWAY
May 27
Regulatory Affairs Specialist required for Galway based medical device company!
Senior Associate - Clinical Trial / Regulatory
Marlow
May 27
This opportunity is for a leading Pharmaceutical & Medical Device company based in Buckinghamshire (not far from West London). As a large pharmaceutical organisation they are focused on discovering, developing and commercialising innovative pharmaceuticals, biologics, medical devices and over-the-counter consumer products.
CONTRACT Senior Medical Writer - Regulatory/Clinical
England
May 27
For a confidential consultation call Meghann Price on 0044 (0) 207 255 6665 or email your CV to meghann.price@secpharma.com Contract/Freelance Experienced Medical Writer - Home-based Regulatory/Clinical
Head of Regulatory Information Systems Management
Harlow
May 26
Have you got a background in Life Science or similar degree? Do you bring a strong eye for detail coupled with an analytical mind, with experience in the pharmaceutical industry? You might be just what we're looking for.Teva are looking for a Head of Regulatory Information Systems Management who will have responsibility for leadership of significant technology and process projects impacting Global Regulatory Affairs and its partner organisations.
Regulatory Affairs pharmacist - France - entry level
France
May 26
Le candidat sera en charge de la validation des dossiers AMM génériques et leurs modifications dans le cadre de procédures centralisés, MRP et décentralisés. Bien d'autres responsabilités seront incluant le controle de la publicité, suivre quantitativement et qualitativement la production et l'approvisionnement etc... (Nous pouvons vous renseigner par téléphone pour les autres missions)
Abteilungsleiter Regulatory Affairs (m/w)
Basel-Country
May 26
Director of Regulatory Affairs (m/w)Office-based in der Nähe von BaselAufgaben:In dieser Position sind Sie verantwortlich für die operative Führung und die Führung der neu geschaffenen Regulatory Affairs Abteilung einschließlich der beiden bereits existierenden RA- Gruppen. Sie sorgen für die zeitnahe Erstellung von regulatorischen Dossiers für unsere pharmazeutische Wirkstoffe (APIs) sowie die nachhaltige Archivierung und Pflege dieser Dossiers bei den Gesundheitsbehörden weltweit. ...
Regulatory Affairs Manager (m/w) APIs
Aargau
May 26
Regulatory Affairs Manager (m/w) APIsOffice-based in Aargau (AG)Aufgaben:? Bearbeitung aller regulatorischen Anliegen für eine Reihe von Wirkstoffen und Darreichungsformen? Selbstständige Koordination und Verantwortlichkeit für die Zusammenarbeit mit zahlreichen Fachabteilungen? Erstellung neuer Drug Master Files und Registrierungsdossiers nach vereinbarten Zeitplänen und den aktuellen länderspezifischen Richtlinien (CH, EU, USA, Japan), sowie Pflege bestehender Dossiers? Vertretung der regu ...
Regulatory Affairs - Leading Consultancy
Den Haag
May 26
My client a leading consultancy delivers projects for more than 250 clients within the (bio) pharmaceutical, Medical Devices and Life Science industry. With projects covering early development to commercial production, you will have the opportunity to work in a wide variety of projects and be in direct contact with clients expanding your scope and understanding within Regulatory Affairs.
Regulatory Affairs Manager - Cosmetics - Nottingham
Nottingham
May 26
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Liver disease - One product in development , one post approval - Cambridge - EU work
Cambridge
May 26
To apply for this regulatory affairs manager please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - AFRICA region- Whole submission experience - Cambridge- Excellent salary and bonus
Cambridge
May 26
To apply for this regulatory affairs associate please call Julie Cooper on 07951 082482 Alternatively please send his CV to:julie@mosaicrecruitment.co.uk
Respiratory Regulatory CMC Manager/Senior Manager
Sandwich, Kent, UK
May 26
Great Opportunity - Respiratory Regulatory CMC Manager/Senior Manager - Mylan Kent, UK
Senior Regulatory Affairs Associate - LATAM role
Cambridge
May 26
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - Must have Middle East and Africa experience - UK - Bucks - 12 months FTC
Buckinghamshire
May 26
To apply for this senior regulatory affairs associate please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Officer - Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
May 26
To apply for this regulatory affairs project manager role you will need to either call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Project Manager - Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
May 26
To apply for this regulatory affairs project manager role you will need to either call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Seniore Regulatory Affairs Consultant - Munich - Biologics , CMC work - Admired consultancy
Munich
May 26
To apply for this senior regulatory affairs role please call Julie Cooper on 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - UK - ROW and EU role
Cambridge
May 26
To apply for this role please call Julie Cooper on 07951 082482. Alternatively please send your CV to :julie@mosaicrecruitment.co.uk
Regulatory Affairs Associate Manager - EU role - Based Uxbridge with one day travel
Uxbridge or Cambridge
May 26
To apply for this regulatory affairs associate manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Officers
Dublin, Republic of Ireland
May 26
Our client, a growing Dublin based pharmaceutical company are currently recruiting for a Regulatory Affairs Officers for permanent and contract roles.
Director for Regulatory Affairs, Biologics
Zürich
May 26
Director for Regulatory Affairs, Biologics, Programme Lead, Lead EU submissions for Biologics in a well backed start-up. 150-200k + Share options + Bonus
Principal Consultant- Regulatory Services
Germany
May 26
My client, a leading Contract Research Organisation, is looking for an experienced CMC Consultant to join their team in Europe.
Senior Regulatory Associate
Marlow
May 26
A leading pharmaceutical company based in Marlow are looking for an interim Senior Regulatory Associate on an initial 12 month contract.
Senior Regulatory Affairs Consultant
Berkshire
May 26
An internationally known biotechnology company situated in Berkshire and operating in over 70 markets worldwide is looking for a Senior Regulatory Affairs Consultant. The company specialises in neurological conditions and puts a great emphasis on team work and delivering biological products. This is a 6 month contract role with the possibility of an extension. ...
OTC Regulatory Director (Pharma, OTC, Consumer Health)
Berkshire
May 26
This is a rare opportunity for a senior level professional to step into a fantastic company. This client is a global leader in the pharmaceutical and consumer health market.As the successful Regulatory Director, you would be tasked with further strengthening the clients' position across the international landscape.
Regulatory Project Manager – EU Locations, or Home Based
England
May 26
A fantastic opportunity has become available, working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level, this company invest heavily to attract and retain high quality staff; this organisation has a very credible reputation for being one of the best employees in its arena. My client invests heavily in talented teams as this is central to their ambitious expansion plans.
Senior Regulatory Affairs Consultant
London
May 26
A large global pharmaceutical company with leading products across various therapeutic areas are looking to hire a Senior Regulatory Affairs Consultant at their office in London, UK. This vacancy is an exciting opportunity to work at a top 10 global pharmaceutical company that employs approximately 100,000 people worldwide. This is a 6 month contract role with the possibility of an extension. ...
Project Manager/Senior Project Manager – Regulatory Affairs
France
May 26
A fantastic opportunity has arisen to join an award winning health care service provider in a home based project manager role. They provide drug discovery, development and lifecycle management services and have presence globally. Their clients and partners include pharmaceutical, biotechnology, medical device, and academic and government organizations.
Regulatory Specialist-Progressive Environment Enabling Growth
Brussels
May 26
Regulatory Specialist-Progressive Environment Enabling GrowthAn organisation who are currently leaders in the field of Medical Technology are looking for a Regulatory Affairs Specialist to join their European Regulatory team. With operations across 50 countries globally and a company ethos of promotion within, you will take the steps to learn, develop and further your career in a supportive environment.
Senior Regulatory Affairs Manager
England
May 26
My client is a leading research-based global pharmaceutical company, and they focus on the discovery, development, manufacturing and marketing of a large variety of top-quality pharmaceutical products. They have recently created this role in London for an experienced senior manager to join their team in order to sustain compliance and aid the company's Marketing Authorisations.
Senior Regulatory Affairs Consultant
Berkshire
May 26
An internationally known biotechnology company has an opening for a Senior Regulatory Affairs Consultant job at their Berkshire office. The company has a strong reputation for developing innovative therapies for neurological diseases and employs approximately 7,000 people worldwide. This is a 6 month contract role with the possibility of an extension. ...
Regulatory Affairs Manager, Bristol, Dynamic
Bristol
May 26
A family owned but extremely well established chemical business is looking for a Regulatory Affairs Manager, to take on a dynamic permanent position.The company is in a great position at the moment and for over a century now have been growing with an impressive international reach, but the culture and feel of a smaller company. The successful candidate will be given the opportunity to liaise with various other departments
Senior Project Manager/Regulatory Manager: Cambridge
Cambridge
May 26
A fantastic opportunity has become available, working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level, this company invest heavily to attract and retain high quality staff; this organisation has a very credible reputation for being one of the best employees in its arena. My client invests heavily in talented teams as this is central to their ambitious expansion plans.
Regulatory Affairs Manager
Rep. Ireland
May 25
We are currently seeking applications on behalf of our client for the role of Regulatory Affairs Manager. A new position within the company, lots of autonomy, great opportunity!
Regulatory Affairs Scientist - Biotech
Cork
May 25
Regulatory Affairs Scientist A leading innovative global Biotech company is currently seeking a Regulatory Affairs Scientist to join their expanding business in their Cork site. This company is committed to further developing its growing portfolio of pharmaceutical products. Their products are marketed to almost 150 countries worldwide and this is a fantastic opportunity for someone looking to progress their career within regulatory affairs. ...
Regulatory Affairs Manager - Needed ASAP
Berkshire
May 23
If working in a fast-paced environment with a wide variety of innovative class I to III devices at the forefront of the industry is where you see yourself, get in touch now!This is a great opportunity within regulatory affairs to join a world leading medical device company based in South East UK on an interim. Join an international regulatory affairs and quality team and gain the opportunity to develop your career on the global platform. ...
Senior Manager of Regulatory Affairs-CMC
Seattle
May 23
A growing pharmaceutical Company headquartered in the Seattle, Washington area is looking for a Sr. Manager of Regulatory Affairs-CMC.  This position offers unprecedented growth opportunities,...
ASAP - The Regulatory Program Manager – 6 months freelance roll
Belgium
May 22
The Regulatory Program Manager will be responsible for Global Regulatory Team (GRT) support.Will represent Regulatory Program Management (RPM) at the GRT translates the Regulatory strategy into realistic and executable Regulatory deliverables with clear assumptions based on GRT input. Works out Regulatory scenarios to support decision making in line with Regulatory and Compound Development Team (CDT) strategy. Will support early risk identification and development of mitigation strategies. ...
Senior Regulatory Affairs Officer
London
May 22
My client, a large pharmaceutical company, is looking for an experienced Regulatory Affairs professional to join they Project Management team. The company is bringing through some of their major pipeline products and are looking for new professionals to join their team. The successful candidate will have exposure to a wide range of Regulatory skills and will be look to be developed within the company.
CMC Regulatory Affairs Consultant – CMC, Contract, Europe – Global Pharma – Bucks
Berkshire, Middlesex, Buckinghamshire area
May 22
Regulatory Affairs, CMC, Contract – Fantastic new contract has opened up for a 6 month contract to join this established, top pharma as a CMC Regulatory Affairs Consultant. The positon, based from their HQ in Buckinghamshire, will see you responsible for CMC Dossier submissions in Europe. The role will be reviewing full dossiers from US submissions, amending as appropriate and ensuring successful completion for EU regulations.
CMC Regulatory Consultant – CMC Dossiers, EU, Global Pharma – Buckinghamshire
Berkshire/Buckinghamshire region
May 22
CMC Consultant, Regulatory Affairs, Contract – An excellent contract for 6 months has become available within this growing, Top 15 pharma business for an EU CMC Consultant. The position is office based in Buckinghamshire, with focus in EU CMC dossier review, working closely with US counterparts and filings for FDA. Requires those with proven background of EU orientated dossier work, able to take ownership on this and review FDA submissions to ensure EU submission success.
Senior Quality and Regulatory Affairs Manager-Consumable Devices
Belgium
May 22
Due to rapid growth, my client, an international healthcare company with an outstanding reputation in the industry, is currently looking to grow their team and currently looking a Senior Quality and Regulatory Affairs Manager with strong experience with Consumer care Medical Devices products to be based in Belgium.
EDMS Regulatory Business Systems Manager - World leading Pharma - Central London
London
May 22
To apply for this EDMS Regulatory Affairs System role please call Julie Cooper on 07951 082482 or send your CV to- julie@mosaicrecruitment.co.uk
Regulatory affairs associate - EMEA work-Buckinghamshire
Buckinghamshire
May 22
To apply for this regulatory affairs associate please call Julie Cooper on :Julie@moaiccrecruitment.co.uk Alternatively please send CV to: Julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Cosmetics - Nottingham
Nottingham
May 22
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
jobs : 100 +
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