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The latest Regulatory Affairs / Reg affairs jobs - BETA

Jobs: Regulatory Affairs / Reg affairs

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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 ...
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
Offaly
May 26
I have an immediate opening for Regulatory Affairs Specialist based in Co. Offaly. This is a 12 month fixed term contract position to work on a specific project as the company continues to grow.
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
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
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. ...
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.
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
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,...
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.
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.
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
Senior Regulatory Affairs Associate - AFRICA region- Whole submission experience - Cambridge- Excellent salary and bonus
Cambridge
May 22
To apply for this regulatory affairs associate please call Julie Cooper on 07951 082482 Alternatively please send his CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - LATAM role
Cambridge
May 22
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 Project Officer- Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
May 22
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 22
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
Regulatory affairs manager - Netherlands - affiliate role - must speak Dutch
Netherlands
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
Regulatory Affairs Associate - Affiliate role - Netherlands
Netherlands
May 22
To apply for this regulatory affairs associate role please call Julie Cooper on 07951 082482 Alternatively please send your CV to: ulie@mosaicrecruitment.co.uk
Regulatory Affairs Associate Manager - EU role - Based Uxbridge with one day travel
Uxbridge or Cambridge
May 22
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 and Patient Safety - Team Leader
Amsterdam
May 22
Do you want a cross-functional position which would give you the possibility to work together with different and diverse departments? My client an innovative Pharmaceutical company with a very interesting and fast growing pipeline is looking for someone who is willing to take the next step to a leading function.
Senior Regulatory Affairs Associate - UK - ROW and EU role
Cambridge
May 22
To apply for this role please call Julie Cooper on 07951 082482. Alternatively please send your CV to :julie@mosaicrecruitment.co.uk
Regulatory Affairs Opportunities, Switzerland
Switzerland
May 22
Regulatory Affairs Opportunities for Pharmaceuticals, Switzerland, Zurich, Basel, Geneva and Bern
URGENT freelance 6 months EU Reg Affairs Manager HIGH RATE
Buckinghamshire
May 22
Hi All,URGENT freelance 6 months EU Reg Affairs Manager **HIGH RATE** 70-90£/hourThe ideal candidate will:Supports the implementation of regulatory strategy in Europe and the EEA and provides regulatory support for the registration and post-licensing activities of medicinal products. Develops and maintains knowledge of EU regulatory procedures .Contributes to the European Regulatory Affairs team. ...
URGENT - Global Senior Regulatory Affairs Manager - Medicines
England
May 22
My Client, a top Consumer Healthcare company are aspiring to find the best Senior Regulatory Affairs Associate to work with them on a global level.
EXCLUSIVE - SENIOR REG AFFAIRS ASSOCIATE
England
May 22
My Client, a top Consumer Healthcare company are aspiring to find the best Senior Regulatory Affairs Associate to work with them on a global level. Their innovative take on the industry has led them to be one of leaders in the field.
Regulatory Affairs Manager CMC (daily rate contract)
Buckinghamshire
May 22
Daily rate contract role: Regulatory Affairs Manager CMC required by client in Bucks until end of year - highly competitive daily rate payable!!
Regulatory Affairs Manager, Gloucester, Dynamic
Gloucestershire
May 22
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
Global Pharma - Regulatory Affairs Associate - Sydney
Sydney
May 22
Global Pharmaceutical Company - Regulatory Affairs AssociateSydney$70,000 - $90,000 plus benefitsOur client are currently the fastest growing pharmaceutical company in Australia in terms of both profit and growth. They have won several awards and have numerous successful brand names. Coming into 2015 they have a solid pipeline with several of the leading drugs in the market.
Regulatory Affairs Manager (m/w)
Hamburg
May 21
Regulatory Affairs Manager m/wOffice-based in der Nähe von HamburgEin dynamisch wachsendes, international tätiges Pharmaunternehmen mit Sitz in Hamburg sucht einen Regulatory Affairs Manager.Aufgaben:? Erstellung und Pflege von Zulassungsdossiers und Qualitätsdokumenten.? Vorbereitung und Durchfürung von Zulassungsverfahren.? Verantwortung für das Lifecycle-Management? Mitarbeit in verschiedenen interdisziplinären Projektgruppen. ...
Regulatory Affairs Specialist – CMC – Belgium
Belgium
May 21
A small and growing pharmaceutical company is looking for a regulatory affairs specialist with focus on CMC. You can use your experience in redaction of CMC variations, registrations and renewals but also gain more experience for pharmaceuticals used in different therapeutic areas.
Regulatory Affairs Manager - Immediate Start
Berkshire
May 21
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. ...
Regulatory Affairs CMC Director
Switzerland
May 21
Regulatory Affairs CMC Director - Small Molecules - Leading Pharmaceutical Group
Senior Regulatory Affairs Specialist-Freedom To Shape Your Work
Antwerp
May 21
Senior Regulatory Affairs Specialist-Freedom To Shape Your WorkMy client, a company who specialise in Molecular Diagnostics is seeking a Senior Regulatory Specialist to join their rapidly expanding Regulatory team. With 2 new people already on board in the team, you will work together to drive the companies new products onto the global market.
Regulatory affairs submissions specialist - Regulatory Operations and Info Management - UK - London- Contract
London
May 21
To apply please send your CV to:julie@mosaicrecruitment.co.uk or call me on 07951 082482
Regulatory Affairs Liaison Manager- Switzerland
Schweiz
May 21
Regulatory Affairs Liaison Manager, Switzerland * You have at least 3 years experience in the area of regulatory affairs and you would like to work for a global biopharmaceutical company? * You have a good understanding of the entire regulatory affairs processes and have worked at a strategic level? * You would like to work for a market leader with innovative products and a very international atmosphere?Then I have a fantastic opportunity for you at a biopharmaceuticals company in Switzerlan ...
Mitarbeiter Regulatory Affairs (m/w)
Frankfurt am Main
May 21
Mitarbeiter Regulatory Affairs (m/w)Office-based im Raum FrankfurtVoll- oder Teilzeit, befristet bis Ende 2015Aufgaben:? Inhaltliche und formale Überprüfung von regulatorischen Unterlagen auf Plausibilität und Eignung für die Zulassungsdokumentation? Umgang mit Publishing Software und selbständiges Erstellen von eSubmissions? Eingabe von Daten in Datenbank? Vorbereitung und Unterstützung bei der Durchführung von Zulassungsverfahren und Einreichung von Änderungsanzeigen)Voraussetzungen:? Erfo ...
Regulatory Affairs Manager CMC - Raum Basel
Basel-Landschaft
May 21
Regulatory Affairs CMC Manager (w/m) Raum BaselFür ein mittelständisches Pharmaunternehmen im Raum Basel suche ich einen Regulatory Affairs CMC Manager (m/w). ...
Regulatory Affairs associate –Career development -Ireland
Republic of Ireland
May 21
My client are a global pharmaceutical company based in Ireland who are currently looking for a Regulatory Affairs associate to join their team on an initial 6 month contract. This is an excellent opportunity for learning new skills and taking on some excellent experience with the chance for repeat contracts.
Regulatory Affairs Officer – Global Pharma – Ireland
Republic of Ireland
May 21
My client is a large pharmaceutical company who are currently looking for a Regulatory Affairs Officer and kick start your career with Regulatory Affairs within Ireland. With this opportunity you will find an excellent chance to learn and develop different skill sets that will springboard your career.
Regulatory Affairs Manager, Zurich Area
Zürich
May 20
Regulatory Affairs Manager, Zurich Area, Broad role with very good commitment for growth and rewards- 140k+
Associate Director for Regulatory Affairs, Biosimilars
Zürich
May 20
Associate Director for Regulatory Affairs, Biosimilars
Regulatory Affairs Manager
Portugal
May 20
My client is a leading bio-pharmaceutical company looking for an enthusiastic Regulatory Affairs professional to join their passionate and innovative team. The ideal individual would deal with the regulatory affairs activities in Spain and Portugal with direct support from the Portuguese Technical Director where you will be ensuring conformance to national and EU drug laws.
Regulatory Affairs Manager - CMC
England
May 20
An exciting opportunity has arisen for a Global Regulatory Affairs Manager to join their thriving team within a global biopharmaceutical organisation.
Senior Regulatory Affairs Manager
England
May 20
Our client is a global market leader in providing biopharmaceutical services. They have extensive therapeutic, scientific and analytics expertise within biopharmaceutical and health sciences.
Senior Regulatory Affairs Manager
England
May 20
A market leading bio-pharmaceutical consultancy company has an exciting new position for a Senior Regulatory Affairs Officer based in the city of London.
Regulatory Affairs Officer
England
May 20
This opportunity is for a leading biopharmaceutical services organisation that has helped develop or commercialize some of the top selling drugs on the market. They have a high focus on dedication to ethics and high quality in the pursuit of success in human measures.
Regulatory Affairs Officer
England
May 20
Our client is a global market leader in providing biopharmaceutical services. They have extensive therapeutic, scientific and analytics expertise within biopharmaceutical and health sciences.
Global Regulatory Affairs Manager
Portugal
May 20
My client is one of the most innovative and dedicated groups within the Pharmaceutical industry today who are looking to extend their Regulatory team on a global basis. The role will play an integral part of their development plans and would influence their product portfolio for years to come.
Global Regulatory Affairs Manager
Portugal
May 20
My client is one of the most innovative and dedicated groups within the Pharmaceutical industry today who are looking to extend their Regulatory team on a global basis. The role will play an integral part of their development plans and would influence their product portfolio for years to come.
Regulatory Affairs Projects – Continuous Growth
Netherlands
May 20
Gain a fantastic varied role within regulatory affairs with a leading organization based in South of the Netherlands. You will be working within a wide range of project from 250 clients within the biopharmaceutical, medical device and life science industry.
Regulatory Affairs pharmacist - France - entry level
France
May 20
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)
Senior Regulatory Affairs Specialist-Global Market Exposure-BE
Antwerp
May 20
Senior Regulatory Affairs Specialist-Global Market Exposure-BEA company who specialise in the field of Molecular Diagnostics are looking for a Senior Regulatory Specialist to join their Regulatory team. My client aim to be market leaders in their field of work and as such are looking to expand their market reach outside of Europe, offering you a position where you will always learn and develop new skills.
Regulatory Affairs Specialist - Orthopaedics
Hertfordshire
May 20
If you woke up this morning wishing you could work with an expansive portfolio of class I to III devices, look no further!My client are a renowned orthopaedics manufacturer that are looking for experienced regulatory affairs professionals to come on board as soon as possible to take part in a variety of projects within the medical devices area. ...
Regulatory Affairs Manager – Relocation Assistance – Austria
Austria
May 20
As Regulatory Affairs Manager you will be responsible for the quality part, mainly module 2.3 and 3, for international submissions. You will be working in life cycle development but also life cycle maintenance. In addition to working on submissions, renewals, and variations, you will be working on CMC strategies and how to improve the regulatory process. Another aspect to you work is the communication with regulatory agencies, including EMA and AGES.
Trainee Regulatory Affairs (w/m) (München - Deutschland)
Munich / München - Germany
May 20
Shared Work – Shared Vision: The way we do business, a promised standard that includes ongoing support from a specialized team dedicated to meeting or exceeding our clients’ expectations. Zur Unterstützung unseres Regulatory Affairs Teams in Deutschland suchen wir zum schnellstmöglichen Zeitpunkt eine/n motivierte/n Trainee (w/m).
Regulatory Affairs Managers wanted in Brussels, Belgium - Global CMC roles covering EU/US//Emg/Japan/LatAm
Brussels, Belgium
May 20
These exciting opportunities will allow you to take the CMC strategic lead for development and marketed products, managing the generation of high quality regulatory submissions .If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Global CMC Project Manager – Brussels -
Brussels, Belgium
May 20
Work on Global CMC projects - Have real autonomy, scope and responsibility for your own varied product portfolio - Receive excellent training & guaranteed career development. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Operations Consultant
Cambridge
May 20
This is a new job opportunity at a biopharmaceutical company focused on developing cancer treatments. They are currently recruiting for an experienced Regulatory Affairs Operations Consultant to join their expanding team in Cambridge. This is an exciting time to join this company who operate across the United States, Europe and other international markets and have an extensive pipeline of products under development. This is a 3 month contract job with the opportunity to extend. ...
Regulatory Affairs CMC Associate Director – Brussels – Strategic CMC role for EMEA regions Salary to 110,000 euros + Car + Bonus
Brussels, Belgium
May 20
Reporting directly into the Global Head of CMC, you will be the CMC lead for your projects, which includes a A Late stage development project & Supporting a Centralized MAA -If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Operations Consultant
Maidenhead
May 20
An internationally known biotechnology company situated in Berkshire and operating in over 70 markets worldwide is looking for a Regulatory Affairs Operations Consultant. The company specialises in neurological conditions and puts a great emphasis on teamwork and delivering biological products. This role will be based in Maidenhead and is a 6 month contract role with the possibility of an extension. ...
Regulatory Affairs Officer; exciting new permanent opportunity
North West
May 20
A great development opportunity has become available for a regulatory professional seeking new challenges in the fast moving generic market. My client is one of the largest generic companies in the UK with over 350 employees and a growing product portfolio; a company that values the importance of professional growth. The permanent Regulatory Affairs Officer position will be office based in the North West of England.
Regulatory Affairs Manager
England
May 19
My client is looking for a Global Regulatory Affairs Manager to join their thriving team. This is an exciting opportunity that would require the successful individual to manage regulatory/technical projects for both internal and external clients. You will also be expected to provide strategic regulatory/technical consultancy on a variety of projects.
Senior Regulatory Affairs Manager (m/w) - Tuttlingen
Tuttlingen
May 19
Senior Regulatory Affairs Manager (m/w) der MedizintechnikOffice-Based in Tuttlingen, DeutschlandIhre Aufgabe• Maintenance and optimization of the quality management system• Assists in strength / weakness analysis of the Quality Management System• Responsible for compliance to all applicable standards• Review and approval of processes, creates/revises procedures and work instructions to ensure these processes are correctly documented• Serves as a checkpoint to ensure procedures are written i ...
Regulatory Affairs Associate
Prague
May 19
Due to our success and expansions we are looking to recruit Regulatory Affairs Associate.
Director EU Regulatory Affairs
Hampshire
May 19
EU Regulatory Strategy Lead - DirectorPermanent JobCompetitive negotiable salary + bonus and benefitsBased in Hampshire, UKCurrently recruiting are global specialty pharmaceutical company who are fast becoming major players in the industry. After a recent restructure and a massive last quarter with increased revenue of 30%, they are now looking for exceptional regulatory affairs professionals to support their up and coming pipeline of products. ...
Regulatory Affairs Specialist - Ophthalmology
Paris
May 19
Key words: Regulatory Affairs, Executive, Officer, Specialist, Associate, LCM, EU, Global, Ophthalmology, MAA, Contract, Interim, Freelance, Paris, France
Regulatory Affairs Professional- CMC
Dublin, Republic of Ireland
May 19
Our client a leading pharmaceutical manufacturing company now have an immediate requirement for a Regulatory Affairs Professional- CMC. This is a full time fixed term contract based in Dublin. Applicants should have a strong knowledge and experience of working with quality documentation for drug products and drug substances.
Regulatory Affairs CMC - Contract
Berkshire
May 19
My client, a global Biopharmaceutical company are searching for a Regulatory Affairs CMC Specialist, to start a 1 year contract, where you can either be based in Belgium or South East England. My client is looking for a consultant with a minimum of 5 years in industry. My client is offering a very competitive hourly rate for this role. For more information and to apply for to this role, please call Richard Williamson on 0203 327 3072 or apply via this advert.
Regulatory Affairs Manager Bei Lübeck, Deutschland FREELANCE
Norderstedt
May 18
Regulatory Affairs ManagerBei Lübeck, DeutschlandFREELANCEKlasse III ProduktAufgaben:• Produktzulassungen auf internationaler und nationaler Ebene• Durchführen von Design Dossies nach CE standard• Erstellen aller nötigen Dokumente für die internationale Registrierung • Erfahrung mit Risikoanalysen nach ISO 14971• Einhaltung von Zertifizierungsanforderungen für Medizinprodukten und deren Zubehör (MDD, FDA, PAL)• Abstimmung aller Tätigkeiten im RA Bereich, • Cross-Funktionen mit den jeweiligen ...
Regulatory Affairs Manager Nord-Deutschland FREELANCE
Lubeck
May 18
Regulatory Affairs ManagerNord-DeutschlandFREELANCE12 MonateIn 90% Home-OfficeAufgaben:• Einhaltung von Zertifizierungsanforderungen für Medizinprodukten und deren Zubehör (MDD, FDA, PAL)• Abstimmung aller Tätigkeiten im RA Bereich, • Cross-Funktionen mit den jeweiligen Fachbereichen• Globale Koordination der Zulassungen • Direkter Kontakt mit globalen Vertriebsorganisationen • Direkter Kontakt mit globalen BehördenIhr Profil: • Abgeschlossenes Studium im Bereich Medizintechnik o.ä. ...
Regulatory Affairs Manager - Established Products
England
May 18
A fantastic and immediate need has arisen at a global pharmaceutical company for a Regulatory Affairs Manager to join the team. You will be responsible for Established Products within your designated therapeutic area (CVM) My client is a research-based global pharmaceutical company, and is amongst the leading pharmaceutical companies in the world.
Regulatory Affairs Specialist/Senior Specialist MDandD
Stevenage, Herts
May 15
Are you an experienced medical device Regulatory Affairs professional? Are you looking for an additional contract in a successful and growing medical device regulatory team where you can demonstrate your prowess in Medical Device Regulatory Affairs. Then Novella Clinical, a Quintiles company, is looking for you.
PW 6317 Interim Associate Director Regulatory Affairs / Senior Regulatory Manager
Oxfordshire
May 15
An opportunity for an experienced Regulatory professional to join a niche biopharmaceutical company at either Associate Director or Senior Manager level. Trials are at Phase I and II stage and require support at an operational level. The position is offered on a 6 to 9 month contract basis. Development experience is required.
Regulatory Affairs Manager
Berkshire
May 15
Regulatory Affairs Manager: Berkshire. Our client is recognised globally as one of the top 10 companies within the pharmaceutical industry, the company have a low turnover of staff, which is testament to their investment in their employees and work environment. Our client is looking for a Regulatory Affairs Manager to provide regulatory support for regulatory submissions, technical files, agency responses and internal informational queries
Global Regulatory Affairs Director – EU, US and RoW regions – Salary to 120,000 + Car + Bonus + Stock Options -South-East
South-East UK
May 15
This role will suit a regulatory professional who is looking for a bigger role with more challenges and the opportunity to work in a Global Head office. You will need strong project management and strong technical capabilities to provide oversight and alignment for global regulatory strategies - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380
Regulatory Affairs CMC Manager
London
May 15
A major biotechnology company, with an extensive pipeline and commercial portfolio in oncology and immunology, currently has an exciting new job opportunity for a Regulatory Affairs CMC Manager to join their West London team. This is an excellent opportunity to join an innovative company that delivers life-changing drugs with over 4,000 employees in over 50 countries worldwide. ...
Senior Associate Regulatory Affairs (Clinical Trials) Contract
Buckinghamshire
May 15
Contract opportunity: Minimum 12 month contract position for a Senior Associate Regulatory Affairs within Clinical Trials to start ASAP with a Global pharma company!
Global Regulatory Affairs Director – EU, US and RoW regions – Salary to 140,000 + Car + Bonus + Stock Options - Brussels
Belgium
May 15
This role will suit a regulatory professional who is looking for a bigger role with more challenges and the opportunity to work in a Global Head office. You will need strong project management and strong technical capabilities to provide oversight and alignment for global regulatory strategies - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore in the UK London office, on +44 (0)207 801 3380
Senior Regulatory Affairs Associate, Clinical Trials Group
Marlow
May 15
• 12 month contract initially (PAYE) – hope to go temp to perm • Leading Pharma company • Office based Marlow • MUST have worked on Clinical Trial Applications, in Regulatory Affairs
SENIOR REGULATORY AFFAIRS OFFICER - UK
England
May 14
Chiltern is looking to recruit a Senior Regulatory Affairs Officer on a permanent basis. This role will ideally be office based in Slough, Berkshire. We may also consider field based options.
Switzerland Reg Affairs Emerging Market Freelancer ASAP
Switzerland
May 14
Hi All,As a Regulatory Affairs consultant (Emerging Market) you will be required to provide your services to an established international company based in Switzerland. ...
Regulatory Affairs Officer
Wrexham
May 14
McGinley Scientific are a recruitment partner for an ever expanding Pharmaceutical Manufacturing Organisation who are currently experiencing a phase of rapid growthWe have been engaged to search the market for an experienced Pharmaceutical Regulatory Affairs Officer.
Senior Regulatory Affairs Consultant
London
May 14
Here we have a brilliant opportunity to join an international biopharmaceutical company as a Senior Regulatory Affairs Consultant at their base in West London. This is an organisation that seek to deliver truly innovative drugs and specialise in cancer treatments and other severe, immune, inflammatory conditions. This is a 6 month contract role with the possibility of an extension. ...
Regulatory Affairs Programme Manager\Associate Director
East Anglia
May 14
Regulatory Affairs Programme Manager\Associate Director Up to £80,000 – flexibility for highly experienced candidates Generous benefits package including car or car allowance Location: East Anglia OR Home Based
Associate Director Regulatory Affairs - RoW/International
London
May 14
A major biotechnology company, with an extensive pipeline and commercial portfolio in oncology and immunology, currently has an exciting new job opportunity for an Associate Director Regulatory Affairs to join their UK, London or Swiss team. This is an excellent opportunity to join an innovative company that delivers life-changing drugs with over 4,000 employees in over 50 countries worldwide. ...
Regulatory Affairs Manager Klasse III - Medizintechnikprodukte
Germany
May 13
Regulatory Affairs ManagerKlasse III MedizintechnikprodukteJapan/ USAFREELANCEIn 90% Home-OfficeAufgaben:• Aktive Hilfe bei der Zusammenstellung aller nötigen Dokumente für eine strategische und schnellstmögliche Produktzertifizierung von Klasse IIa/ III Produkten der Medizintechnik in China & Brasilien• Start: Juni´15• Zeitraum: 12 Monate• Ort: 90% Home-Office Ihr Profil: • Abgeschlossenes Studium im Bereich Medizintechnik o.ä. ...
Contract CMC Manager/Regulatory Affairs
City of London
May 13
Our client is looking for an experienced contract Regulatory CMC Manager to join their team. Our client is looking for an contractor with a wide range of experience to come and support upcoming submissions in the CMC department.
Senior Director Regulatory Affairs
City of London
May 13
Our client is looking for an experienced Director in Regulatory Affairs professional to join their Global team. The client is looking for a high level manager that can work closely with different Regulatory teams to ensure projects are met.
Regulatory Affairs/Regulatory Officer
City of London
May 13
Our client is looking for an experienced Regulatory professional to join their international team. The client is looking to launch new oncology and CNS products and need experienced regulatory professionals to manage some hands on submissions.
Regulatory Affairs Specialist
Clare
May 13
I have immediate opening for a Regulatory Affairs Specialist with a leading medical device company based in Co Clare. This is a maternity cover backfill position (9-12 month contract) with a company that is undergoing major growth and offer fantastic opportunities for career progression
Regulatory Affairs Associate (Food Supplements, Vitamins) £35k
Derbyshire
May 13
Regulatory Affairs Associate - (Food Supplements, Vitamins, FMCG) - £35k - MidlandsAbout the role:My client is a leading vitamins & supplements manufacturer, with some instantly recognisable brands.
Regulatory Affairs Associate
London
May 13
An attractive job opportunity has arisen at a leading multinational pharmaceutical company who are seeking a Regulatory Affairs Associate to work at their UK site in West London. The company employs 100,000 personnel across 150 countries, working across multiple therapy areas including cardiovascular, oncology, and respiratory. This is a 6 month contract role with the possibility of an extension. ...
Regulatory Affairs Associate-contract
Cork
May 13
Reporting to the Regulatory Affairs & Laboratory Section Manager, you will thrive in an environment where your natural talents of attention to detail, responsibility, adherence to standards and regulations, your ability to think and act independently; and your flexible and adaptable approach to work will be key.
Senior Regulatory Affairs Associate - LATAM role
Cambridge
May 12
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 Affairs Specialist
Bolton
May 12
A medical device company based in Bolton are looking for an interim regulatory affairs professional to assist them on an initial 6 month contract. The role will involve compiling technical files for a range of devices and also working on new product development projects. They are looking for someone to assist with the projects as soon as possible.
Regulatory Affairs Manager (m/w), Option auf Teamleitung
Baden-Württemberg
May 12
510(k), FDA, MPG und ISO 13485 sind Ihnen ein Begriff?Sie sind interessiert an einer neuen Herausforderung?Dann bewerben Sie sich bei einem Global Player aus der Medizintechnik-Branche mit Sitz in Baden-Württemberg und übernehmen Sie ein spannendes Aufgabengebiet alsRegulatory Affairs Manager (m/w) mit Option auf TeamleitungsfunktionWo: Baden-WürttembergWann: Ab sofortWas bietet das Unternehmen? * Exzellente Entwicklungsmöglichkeiten durch regelmäßige Fortbildungen und Seminare * Modernste T ...
Director, EU Regulatory Affairs - Drugs and Biologics CHF160k+
Lausanne
May 12
SEC is currently working closely with an outstanding worldwide consultancy firm to find an exceptional Regulatory Professional to join their team. Starting in France, with one individual who had a vision to provide excellent life science consultancy to the drug development innovators of the world, they have grown into one of the most respected consultancies in the industry with Offices in in the UK, Singapore, Switzerland and the USA. ...
3. Regulatory Affairs Manager
North Brabant
May 12
For one of our Key Clients in the Netherlands, located in Noord-Brabant, I am looking for a Regulatory Affairs Manager (Medical Device) OrganisationThis organisation is one of the Top 5 Medical Device companies in the world, located in the Netherlands. PositionYou will be part of a driven and enthusiastic team of 4 people who work together in an open culture. The position is very hands-on regarding regulatory submissions and contact with the authorities. ...
Switzerland Reg Affairs Emerging Market Freelance Contract ASAP
Switzerland
May 11
Hi All,A Regulatory Affairs Emerging Market Freelance Contractor is required to join a successful international company based in Switzerland.The role is office based and the ideal candidate will be expected to:- Manage and execute successful regulatory strategies in cooperation and alignment with Commercial Operations Regional and Local Regulatory Managers (RRM/LRM) throughout the product lifecycle for the allocated products/sub-region Emerging Europe Middle-East Africa (EEMEA). ...
Senior Regulatory Affairs Executive
England
May 11
As we go from strength to strength, we are looking to grow our Regulatory team in the UK. These roles will be based from our Head Office in Maidenhead; however you will be required to work at client sites depending on business requirements.
Director, Regulatory Affairs - France
Paris, France
May 11
Pharm-Olam International are a privately owned, mid-sized global Clinical Research Organization (CRO). With Headquarters in Houston, TX, Pharm-Olam has a global presence in over 40 Countries and since being established in 1994 Pharm-Olam have offered clients a wide range of comprehensive, clinical research services in phase I to phase IV trials. For more information about Pharm-Olam please visit our website, www.pharm-olam.com
Quality Management and Regulatory Affairs Specialist
Heidenheim
May 11
I am working with a global leader in the medical device, healthcare and hygiene industries, employing over 10,000 people across the world.
Global Pharma - Regulatory Affairs Manager
Sydney
May 11
Global Pharmaceutical Company - Regulatory Affairs ManagerSydney$160,000 - $200,000k + super + bonusManaging a team of 5 across Regulatory and PharmocovigilanceWorking with a global pharmaceutical company this is a fantastic opportunity to join a highly experienced team as their Regulatory Affairs Manager. The successful candidate will be working on several new products across a number of therapy areas including a range of Biological Drugs.
Regulatory Affairs Officer - Midlands - junior role - must have at least 6 months regulatory experience
Nottingham
May 8
To apply for this role please 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 8
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 8
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
Head of Regulatory Affairs - Middle East and North Africa Dubai-based
Dubai-based
May 8
Head of Regulatory Affairs - Middle East and North Africa Dubai-based
Regulatory Affairs Manager
Rep. Ireland
May 8
Our client a leading healthcare company now have a new opportunity for a Regulatory Affairs Manager to join their organisation. Based in Dublin this is a full time permanent opportunity.
Regulatory Affairs CMC Manager - Biotech - Bavaria
Bayern
May 8
For a biotech company in Southern Bavaria, I am looking for a Regulatory Affairs CMC Manager. This is an exciting opportunity at an entrepreneurial, innovative and agile small company that has the financial backing of a major pharmaceuticals company. ...
Senior Director, Regulatory Affairs, Head of Projects Team (Switzerland or UK based) Job
BOUDRY, Neuchâtel, Switzerland
May 8
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. ...
Associate Director Regulatory Affairs
Parsippany
May 7
Our client is a Global Pharmaceutical company that is offering the right incumbent the opportunity to work on brand-new molecular entities, hands-on experience with FDA...
Regulatory Affairs Manager
Zentral Schweiz
May 7
Unser Kunde sucht zum nächstmöglichen Zeitpunkt einen Regulatory Affairs Manager
Regulatory Affairs Director The Netherlands Manage global regulatory submissions for an expanding Pharma company - Salary to 150,000
The Netherlands, The Hague
May 7
You will manage a small RA team for a company with excellent sales and 1st class resources in a role which will be varied, broad-based and cover all strategic aspects of EU and global development and filings. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg on +44 (0)207 801 3380
Regulatory Affairs Associate Director - Belgium - Take the lead for NME’s (Strategy, Scientific advice and Agency liaison) and become a GRL within 3 years
Belgium, Brussels
May 7
Provide EU leadership into global project teams & • Become a GRL within 2 to 3 years. Take the lead for NME’s in development (Strategy, Scientific advice & Agency liaison) & Take the lead for Centralised MAA’s. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Senior Manager Global CMC - Brussels - Great Salary and full Re-location Packages Available
Brussels, Belgium
May 7
You will need at least 5 years of Regulatory affairs CMC experience and be ready for a role where you have real autonomy, scope and responsibility for your own varied product portfolio, managing multiple products in multiple countries. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380
Astellas – Regulatory Affairs Group Lead (LCM) - Graded Director or Senior Director
Leiden, The Netherlands
May 7
First and foremost, this is a people management role to steer the future growth of an expanding team, to support the new therapy area aligned structure. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore on Matt Grieg on +44 (0)207 801 3380
Regulatory Affairs Director EMEA - Lead the development strategy and L/Cycle management of a Global Brand
Brussels, Belgium
May 7
There focus is always on Innovation, co-creation, thinking outside of the box and reinventing ways of doing things to develop drugs where medical needs remain unmet. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Project Manager - Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
May 6
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 6
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
Regulatory Affairs Officer - Midlands - junior role - must have at least 6 months regulatory experience
Nottingham
May 6
To apply for this role please 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 6
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
Senior Regulatory Affairs Manager (m/w) - Freiberufler
Germany
May 6
Senior Regulatory Affairs Manager (m/w) der MedizintechnikSüddeutschland6 to 8 Monate; Teilzeit mit Home-office optionIhre Aufgabe• Produktzulassungen auf internationaler und nationaler Ebene• Durchführen von Design Dossies nach CE standard• Erstellen aller nötigen Dokumente für die internationale Registrierung • Erfahrung mit Risikoanalysen nach ISO 14971• Erfahrung mit EN ISO 62366• Erfahrung mit EN ISO 60601 3rd edition• Machbarkeitsanalyse und Design-Reviews• Testplänen erstellen und Pro ...
Regulatory Affairs Associate
San Rafael
May 6
This position's primary focus is the formatting, publishing, transmission and archival of submissions to Regulatory Agencies.
PW 6300 Regulatory Affairs Manager / Labelling Manager
Cambridgeshire
May 6
Opportunity for a regulatory consultant to join this exciting pharma company based in Cambridge as their Labelling Manager. You’ll take responsibility for European Labelling, including PILs, CCCDs, maintain records within database and provide internal expertise. Labelling experience is desirable, however not essential if you do have exposure within your regulatory experience.
Head of Quality Assurance and Regulatory Affairs, Munich
München (Kreis)
May 6
For a company in the pharmaceuticals industry in Munich I am currently looking for a Head of Quality Assurance and Regulatory Affairs. If you have management experience in the area of quality and regulatory and are looking for a challenging role at an international company, then this could be the next step in your career. ...
Regulatory Affairs Officer - Midlands - junior role - must have at least 6 months regulatory experience
Nottingham
May 6
To apply for this role please 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 6
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 Manager
London
May 6
My client, a very well established Regulatory Affairs consultancy are searching for a Regulatory Affairs Manager to join their expanding team. The role is permanent, you will be managing a team of 4 consultants, in a vibrant and dynamic office based in the South of England. This is a great opportunity if you are serious about furthering your Regulatory Affairs career.
Regulatory Affairs Project Manager -UK Pharma
England
May 5
Oversees the preparation of Marketing Authorisation Applications (MAAs), variations and Product Information and manages the Regulatory interaction with all Marketing Partners. Responsible for all Regulatory maintenance activities. The job holder will manage a small Regulatory team.
Senior Regulatory Affairs Associate - UK Pharma - North West
England
May 5
A fantastic opportunity has arisen for a Senior Regulatory Affairs Officer to join a growing Pharmaceutical company in the North West of England. This is a great position for someone who is looking to grow with a company and gain some valuable experience.
Regulatory Affairs Associate - Contract - Large Pharma - UK
England
May 5
This is a fantastic opportunity for an experienced CMC contractor to join one of the world’s leading Pharmaceutical companies.
Regulatory Affairs Associate - Large CRO - UK
England
May 5
A fantastic opportunity has arisen for a Senior Regulatory Affairs Associate to join the world’s leading CRO. In this role you will be required to prepare and/or review regulatory submissions to support clinical trial and marketing authorisation activities for either internal and/or external clients. Providing regulatory support for assigned projects.
Senior Regulatory Affairs Officer - CRO - London
England
May 5
An exciting opportunity has arisen for a Senior Regulatory Affairs Officer to join one of the world’s leading CROs in their London Branch. This position can offer the successful candidate some great experience and opportunities to progress further in their career.
Regulatory Affairs Manager - Interim, 80%, on site, Norddtl.
Hamburg
May 5
Aktuell suche ich für einen unserer Kunden, ein global agierendes pharmazeutisches Unternehmen, einen Regulatory Affairs Manager - Interim (m/w).
Specialist in Regulatory Affairs (Medical Devices) – Hamburg – 6-month contract – €300 p/d
Germany
May 5
Optimus Search are working with a medical devices company to find a Regulatory Affairs Specialist to join their team based in Hamburg. The right candidate with take full responsibility for all global regulatory submissions and be the point of contact for global regulatory Authorities. Therefore must have strong knowledge of ISO 13485 and other relevant regulations associated with medical devices.
Regulatory Affairs Manager, CMC, Leading Pharma, Netherlands
West Netherlands
May 5
An exciting new and unique opportunity has become available for an experienced regulatory CMC professional to join a leading pharmaceutical company. The company is well known for its commitment to developing market leading products and to developing staff to reach their maximum potential. The position on offer is at Regulatory Affairs Manager level on a permanent basis, at the company's office in West Netherlands.
Regulatory Affairs Officer - Midlands - junior role - must have at least 6 months regulatory experience
Nottingham
May 2
To apply for this role please 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 2
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
Regulatory Affairs Project Manager - Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
May 2
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 Manager - Cosmetics - Nottingham
Nottingham
May 2
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
Seniore Regulatory Affairs Consultant - Munich - Biologics , CMC work - Admired consultancy
Munich
May 1
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
Regulatory Affairs Project Manager - Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
May 1
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
Senior Regulatory Affairs Manager
Utrecht
May 1
Due to fast growth, a manufacturer of innovative medical devices, located in the middle of the Netherlands is looking for a Senior Regulatory Affairs Manager. In this complete new position you will be the European lead and be in contact with your American colleagues on a regular basis. ...
Regulatory Affairs Specialist
Leeds
May 1
A leading medical device company based in Leeds are looking for an interim Regulatory Affairs Specialist on an initial 6 month contract. The role will involve compiling technical files in accordance with the requirements of the Medical Device Directive 93/42/EEC. You will be required to co-ordinate with other Regulatory Affairs Associates and personnel in all departments.
Regulatory Affairs Manager
North East
May 1
A leading IVD company are looking for an RA Manager on an interim basis on an initial 3 - 6 month contract.
Regulatory Affairs Specialist
Leeds
May 1
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 Affairs Executive - Pharmaceuticals
Wrexham
May 1
A Regulatory Affairs Executive is required to join an expanding team, on a permanent basis for a large and successful global Pharmaceutical company.The rapid growth of the company in the UK means that an ability and willingness to put your hands to most things in the Regulatory field is a prerequisite. With fantastic training and development on offer this is an excellent opportunity to gain a broad experience in all aspects of Regulatory Affairs.
Regulatory Affairs Manager - N West
North West England
May 1
Our client is a highly regarded medical device company that specialise in the Infection Control, Wound care and Surgical consumables marketplace.In the role of RA Manager, you will come with 5-10 years experience in the medical device/pharmaceutical industry and also have some exposure to European regulations.
International Regulatory Affairs – Markets and Compliance Manager - STRONG COSMETICS EXPERIENCE NEEDED - Midlands
Midlands
Apr 30
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 Operations Manager - South East
Cambridge
Apr 30
To apply for this regulatory affairs operations manager please call Julie Cooper on 07951 082482 or email her on : julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Liver disease Cambridge - EU work
Cambridge
Apr 30
To apply for this regulatory affairs manager please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Cosmetics - Nottingham
Nottingham
Apr 30
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
Senior Regulatory Affairs Associate - AFRICA region- Whole submission experience - Cambridge- Excellent salary and bonus
Cambridge
Apr 30
To apply for this regulatory affairs associate please call Julie Cooper on 07951 082482 Alternatively please send his CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - LATAM role
Cambridge
Apr 30
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
Apr 30
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 - Midlands - junior role - must have at least 6 months regulatory experience
Nottingham
Apr 30
To apply for this role please 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
Apr 30
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
Various Director Level Regulatory Affairs opportunties
London
Apr 30
I am currently recruiting for various Associate Director/Director level Regulatory Affairs positions currently.
Regulatory Affairs - Biozide - Hamburg gesucht
Hamburg
Apr 30
Für ein mittelständiges Chemieunternehmen in Hamburg, suche ich absofort einen Experten (m/w) im Bereich der Zulassung von Desinfektionsprodukten. In Ihrer Rolle vertreten Sie das Unternehmen in externen Gremien und führen ein kleines Team. ...
Quality und Regulatory Affairs Manager (m/w) Medical Device
Geneva
Apr 30
Quality und Regulatory Affairs Manager (m/w) Medical DeviceFreiberufler/FreelancerBei Genf12 Monate, VollzeitAufgaben:• Quality Project Lead in den Projekttätigkeiten der F&Es Abteilung• Erstellen der regulatorischen Projektanforderungen unter DIN EN ISO 13485• Abteilungsübergreifende Aufgaben mit “clinical team” zur Einführung von klinischen Strategien für eine 510(k) Einreichung• Team Verantwortung für die Erstellung der technischen Dokumentation • Entwickeln der Projektstruktur für Zielve ...
Regulatory Affairs Analyst - North West
North West England
Apr 30
Our client is a highly regarded medical device company that specialise in the Infection Control, Wound care and Surgical consumables marketplace.This role will be responsible for the continuous review of applicable laws and regulations, to ensure implementation and ongoing review of procedures and routines for correct handling of all applicable tasks within GDP/GMP and Regulatory Affairs.
Regulatory Affairs Strategist CMC
Basel, Switzerland
Apr 30
A business critical role with direct responsibility for linking Genpact Pharmalink and the Client in a true outsourcing partnership.
Regulatory Affairs Consultant, CMC, Permanent, Consultancy, Netherlands
West Netherlands
Apr 30
My client offers international consultancy services to reputable clients in various sectors, including the Pharmaceutical Industry. They’re currently seeking experienced regulatory professionals with particular expertise in CMC and a keen interest in consultancy to work on key pharmaceutical and biotech projects.
Regulatory Affairs Manager (m/w) - Basel
Basel
Apr 29
Regulatory Affairs Manager (m/w) Medical DeviceFreiberufler/FreelancerBei Basel18 Monate, VollzeitAufgaben:• Überprüfen & Erstellung der Gebrauchstauglichkeit (IEC 62366:2007/60601-1-6)• Erstellung nötiger Zulassungsdokumente von Medizinprodukten 21CFR820• Erstellen einer Risikomanagementsysteme Analyse (EN ISO 19471)• Optimierung des QS-Systems für die europäische Tochtergesellschaft eines international agierenden Medizintechnikunternehmens• Entwicklung, Umsetzung regulatorischer VorgabenIh ...
Regulatory Affairs Associate
London
Apr 29
My client, a rapidly growing Pharmaceutical company, who have a main focus on Generics products are looking for a Life Sciences Graduate who has around 1 year in industry, preferably working in Regulatory Affairs, to join their team. The role is permanent, it is based in the South East of England is offering fantastic career progression for the successful candidate. For more information please contact Richard Williamson on 0203 327 3072 or apply to this advert.
Regulatory Affairs Associate/Manager, Clinical Development
Dublin, Ireland
Apr 29
My client is a specialist consultancy made up of a number of experienced regulatory professionals. The company offers broad regulatory services for clinical trials, medicinal products, medical devices and cosmetics. Currently in demand as a result of this dynamic company’s expansion is a Regulatory Affairs Associate/Manager to be office based in Dublin.
Regulatory Affairs Manager \ Regulatory Project Manager
East Anglia
Apr 29
Regulatory Affairs Manager \ Regulatory Project Manager Location: East Anglia / Home Based. £50,000 - £62,000 per annum – flexibility for highly experienced candidates Our client is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our client has the luxury of working with clients/partners in many different leading organizations.
Regulatory Affairs Director-Oncology
Chicago Bmc
Apr 28
Our client is looking for a Regulatory Affairs Director to head the Clinical functions for Oncology-based pharmaceuticals. Please enquire for more details. 
Regulatory Affairs Project Manager - Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
Apr 27
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 Operations Manager - South East- eCTD , Publishing , Operations , Submissions - Excellent role in exceptional company
Cambridge
Apr 27
To apply for this regulatory affairs operations manager please call Julie Cooper on 07951 082482 or email her on : julie@mosaicrecruitment.co.uk
International Regulatory Affairs – Markets and Compliance Manager - STRONG COSMETICS EXPERIENCE NEEDED - Midlands
Midlands
Apr 27
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 - Cosmetics - Nottingham
Nottingham
Apr 27
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
Senior Regulatory Affairs Associate - AFRICA region- Whole submission experience - Cambridge- Excellent salary and bonus
Cambridge
Apr 27
To apply for this regulatory affairs associate please call Julie Cooper on 07951 082482 Alternatively please send his CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - LATAM role
Cambridge
Apr 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
Senior Regulatory Affairs Associate - Must have Middle East and Africa experience - UK - Bucks - 12 months FTC
Buckinghamshire
Apr 27
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
Senior Regulatory Affairs Officer - Nottingham - CMC , Clinical , CTA experience
Nottingham
Apr 27
To apply for this senior regulatory affairs officer please call Julie Cooper on 07951 082482 or alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Officer - Midlands - junior role - must have at least 6 months regulatory experience
Nottingham
Apr 27
To apply for this role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Officer - Nottingham - CMC , Clinical , CTA experience
Nottingham
Apr 27
To apply for this senior regulatory affairs officer please call Julie Cooper on 07951 082482 or alternatively please send your CV to: julie@mosaicrecruitment.co.uk
VP Regulatory Affairs - Consulting
Any European location - Home or Office based
Apr 26
This is a new position due to the growth of my client. They are looking for an experienced Regulatory candidate to Lead their European team. The right level of candidate will be a Director / Senior Director / Vice President Regulatory Affairs. You will be well connected within the industry, coupled with a strong background of advising clients and delivering high calibre project work.
PW 6294 EU Systems and Publishing Associate / Regulatory Affairs
Hertfordshire
Apr 23
This is a fantastic opportunity to gain exposure to a wide range of key stakeholders across business functions. You play a key role in helping to develop and improve a variety of different software and systems within a global regulatory environment. This is a newly developed role managing submission dispatch to all affiliates, logistics and systems work and will include back up and support to all regulatory publishing activities.
Senior Director, Regulatory Affairs - Hertfordshire
Hertfordshire, Welwyn Garden City, Hatfield Herts
Apr 23
As Senior Director, Regulatory Affairs the incumbent will be the Deputy Head for the Neuroscience & General Medicines (NGM) Therapeutic Area (TA). Duties to include: 1. Manage the EU NGM TA budget. 2. Attend EU Health Authority meetings as NGM TA representative. 3. Monitor the EU regulatory environment & assess implications for NGM products 4. Advice NGM TA Heads on emerging regulatory trends in EU
Global Franchise Head, Regulatory Affairs
England
Apr 23
Objectives and Scope of Position   Provides leadership and strategic regulatory oversight for their designated franchise across the projects portfolio Provides line management, people development, and performance management for their designated franchise Global PDR representative on TA Franchise for designated disease area and provides regulatory leadership to decisions specific to the designated franchise Member of relevant PDR TA leadership team Provides leadership t ...
Associate Director, EMEA International Regulatory Affairs - Based in UK or Switzerland. Job
Hillingdon, England, United Kingdom
Apr 20
POSITION Associate Director, EMEA International Regulatory AffairsSUPERVISOR Director, EMEA International Regulatory AffairsDEPARTMENT Regulatory Affairs EMEALOCATION Celgene R&D, Switzerland or Celgene Europe, UKPREREQUISITES• Bachelor’s degree in scientific discipline or equivalent required• Significant experience in Regulatory Affairs (RA) and International RA and an in-depth understanding of the International regulatory landscape• Line management experience preferredSUMMARYResponsible fo ...
Regulatory Affairs Specialist - Medical Devices
Berkshire
Apr 17
Regulatory Affairs Specialist - Medical Devices. Berkshire. Regulatory Professionals are pleased to be representing a genuine leader in the medical devices and diagnostics field in their search for a part-time Regulatory Affairs Specialist for a 9 month contract. The Regulatory Affairs Specialist will report into the Director of Strategic Regulatory Affairs for the UK and Ireland and will take responsibility of guaranteeing that the regulatory requirements are met throughout the UK and Ireland
Regulatory Affairs Specialist
Ireland
Apr 17
Regulatory Affairs Specialist. Galway - Ireland On-going contract - 0.5 FTE / Part Time An Exciting opportunity with an expanding Medical Device Manufacturers in Ireland has become available for an RA Specialist with a year or mores experience to join them on an on-going part time contractual basis.
Project Manager, Regulatory Affairs (Post Licensing) - EMEA-116915
Asia Pacific
Apr 17
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...
Regulatory Affairs Associate
Rep. Ireland
Apr 16
With 5 commercial products, 7 more in the pipeline and over half a billion dollars of revenue, a global footprint in 40 countries, and a personal connection to our patients, BioMarin is the recognized industry leader in rare disease development. Come work in an entrepreneurial environment where you’ll have the resources and infrastructure combined with visibility and opportunity to tangibly impact patent’s lives and the future of our company. This is your chance to be part of something amazing!
Senior Manager, Global Regulatory Affairs MEA
Bavaria
Apr 16
SEC is currently collaborating with a major global generics company (part of a bigger healthcare group) whose affordable medicines are currently available to 90% of the world's population.I have personally been tasked with find an inovative, stategic thinking regulatory professional to join their Global Regulatory Affairs Department within the MEA team at Senior Manager Level. ...
Regulatory Affairs Snr Manager Wanted for a Top Ten 20 Pharma Company – The Netherlands – Salary 90,000 + Bonus -
The Netherlands
Apr 15
Provide strategic leadership for MAA’s, lifecycle & development projects - The culture here is friendly, positive and has a real feel of self-improvement and you will be taught/mentored by a Snr RA Director with a number of successful RA strategies and submissions behind him. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore on Matt Grieg on +44 (0)207 801 3380
Senior Regulatory Affairs Executive
Berkshire
Apr 15
Senior Regulatory Affairs Executive. Berkshire A leading Global Pharmaceutical company currently requires an experienced Regulatory Affairs professional to join their Consumer division. Working from Pre-Approval to Post-Approval on new and established products, this job offers broad responsibility in a position considered to be the first step into management within the company.
Regulatory Affairs Lead - Medical Devices
Gloucestershire
Apr 14
My client is searching for a Regulatory Affairs Lead to join their exciting company. As a leading supplier of single use Medical Devices to the global market and they have an innovative and very exciting product portfolio, which has been updated and expanded in line with technological advances. At the core of their philosophy is the drive to develop products, which satisfy the current and future needs of both patients and healthcare professionals.
Regulatory Affairs Associate Director / EU and Global Strategy and Project Management - Belgium
Brussels, Belgium
Apr 14
My client has exciting products and challenging project work. It’s a company with a very good growth rate and has a promising future. They have lots of products in the pipeline which means more growth and exciting times are ahead. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs CMC Global Regulatory Liaison roles MAbs and Vaccines Great Salary, re-location and Career Development Belgium
Brussels
Apr 14
If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Regulatory Affairs Senior Manager CMC Biologicals Brussels Provide Strategic leadership for CMC Bio projects Excellent pipeline
Brussels
Apr 14
My client is seeking professionals who can show leadership, high level influencing and persuading with an excellent cross-cultural awareness and understanding of the regulatory framework.Excellent salary and a broad based role. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Managers wanted in Basle Switzerland- Global CMC roles covering EU/US/Japan/Emg/Japan/LatAm – Salary to 150,000CHF + Bonus
Switzerland
Apr 14
These exciting opportunities will allow you to take the strategic lead for marketed products, managing the generation of high quality regulatory submissions required for the filing of technical changes to health authorities globally. 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)207 801 3380
Regulatory Affairs Senior Global CMC Specialist / Switzerland – Global Projects – Excellent Salary – Fantastic Company…
Switzerland
Apr 14
This Global CMC department provides leadership for commercialized products and your role will be to operate as the Regulatory project lead for interactions with all major global regulatory agencies. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Senior Regulatory Affairs Officer \ Regulatory Affairs Project Manager
Berkshire
Apr 13
Senior Regulatory Affairs Officer \ Regulatory Affairs Project Manager Permanent – Part time; 3 days per week. The company are global leaders within prevention, diagnosis and treatment of allergies and are in partnership with other global pharmaceutical companies to develop new treatments. They have a hard working, dedicated culture that is looking to commit to the long term development plans.
Regulatory Affairs Manager - Global Pharma - Sydney
Sydney
Apr 13
Global Pharmaceutical Company - Head of Regulatory - Regulatory Affairs ManagerSydney$160,000 - $230,000k + super + bonusWorking with an award winning global pharmaceutical company this is a fantastic opportunity to join a highly experienced team heading up their Regulatory Affairs Department as their Regulatory Affairs Manager. The successful candidate will be looking after their Oncology, Diabetes and General Medicine portfolios.
PW 6283 Director/Senior Director Regulatory Affairs
Hertfordshire
Apr 10
This is a key opportunity for an experienced regulatory professional to play a Deputy Head role with broad responsibility for the Neuro and General Medicines therapy area of this global Pharma company. You will hold budgetary responsibility, attend key EU Health Authority meetings, play the EU regulatory lead for key General Medicines development projects and closely monitor the regulatory environment.
Regulatory Affairs Associate Director - CMC
Berkshire
Apr 8
Regulatory Affairs Associate Director - CMC Location: Berkshire Reference: J16839 Salary: £65,000 - £85,000 per annum - negotiable dependant on experience Employment type: Permanent
Regulatory Affairs Specialist - 12 Month Maternity Cover-120887
Belgium
Apr 8
PPD has a new vacancy for a Regulatory Affairs Specialist. This opportunity is for 12 month maternity cover. In this role you will provide regulatory advice and carry out projects in the provision of regulatory affairs services. You will also act as liaison with internal and external clients in the provision and marketing of regulatory affairs services. ...
Head of Regulatory Affairs EU and International
Dublin, Republic of Ireland
Apr 7
On behalf of our client, a global pharmaceutical company, we are currently recruiting for a Head of Regulatory Affairs EU and International.
Regulatory Affairs Specialist/Senior Regulatory Affairs Specialist - EMEA-122360
France
Apr 7
PPD is recruiting for Regulatory Affairs Specialists. In this role you will provide regulatory advice and carry out projects in the provision of regulatory affairs services. You will also act as liaison with internal and external clients in the provision and marketing of regulatory affairs services. ...
Regulatory Affairs CMC Bio "Snr Manager" - Global CMC role that covers all phases of development - Expanding company with great opportunities
Belgium, Brussels
Apr 2
This organisation has a fantastic portfolio of products in development so you will have a great platform from which to take the lead in your projects. Based in Brussels, Belgium you will be working from the EU headquarters in a role that covers all major regions. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Global CMC Project Manager – South-East - Global Role with the opportunity to gain Bioteh exp.
South-East
Apr 2
***Be the voice for RA CMC Strategy in development & through MAA’s***• Be the voice for RA CMC Strategy in development & through MAA’s***Be the voice for RA CMC Strategy in development & through MAA’s***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)207 801 3380
Regulatory Affairs Manager / Snr Manager – West London/Berkshire - Salary to £70,000 + Bonus
London/Berkshire
Apr 2
This is a real learning company, one where you will have a succession plan and real career development. 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)207 801 3380 -
Regulatory Affairs Contract Role – Early Phase Development Projects for Orphan Products {Oncology and Immunology} - To £75per hour
Berkshire, Maidenhead or Uxbridge
Apr 2
You will working with an experienced Director to provide hands on leadership and support in a varied role which will include preparing, reviewing and compiling regulatory Early phase applications. 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)207 801 3380
Regulatory Affairs Snr Manager in EU Development – Berkshire – Expanding Pharma with a great portfolio - Pharma and Biotech products
Berkshire
Apr 2
This is an excellent role for those that seek autonomy and want to work with an organisation that see career development and succession planning as essential for people to grow and develop their expertise. 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)207 801 3380 -
Associate Director, Regulatory Affairs - Chemistry, Manufacturing, and Controls (CMC)-122323
England
Apr 2
PPD has a new vacancy for an Associate Director, Regulatory Affairs. The ideal candidate will be an international regulatory CMC professional, and will be responsible for human pharmaceutical products, encompassing small and large molecules, injectable devices, investigational and marketed products, as assigned. ...
Regulatory Affairs Global CMC Roles - Brussels - Great Salary and full Re-location Packages Available - Gain Biologicals exp.
Brussels, Belgium
Apr 1
The organisation is extremely active in the international markets and has been ensuring all their major drugs are registered in all major and emerging markets worldwide. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Associate Director Oncology – Take strategic leadership for mid and late development and new EU and RoW submissions
Brussels
Apr 1
Take responsibility for a mid and stage development pipeline of Oncology NME’s, operating as the regulatory voice for Scientific advice and EU and Row submissions - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Associate Director – EU/US development role - Based in the M4 corridor with a Great Salary available and Full re-location package
Maidenhead
Apr 1
Regulatory Affairs Associate Director – EU/US development role - You will be involved in Scientific advice and providing global regulatory strategy. 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)207 801 3380
Regulatory Affairs CMC Manager – Maidenhead - A role with Scope and Variety covering Pre and Post activities for EU
Maidenhead
Apr 1
This role covers Global registrations and my client is happy to provide excellent training for an RA CMC manager who has the capacity, attitude and approach to learn and develop their expertise. These roles are good mix of strategic input, global project management and cover development and marketed products. 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)207 801 3380
Regulatory Affairs Snr Manager and Associate Director Roles - The Netherlands (close to Amsterdam)
The Netherlands - close to Amsterdam
Apr 1
This organisation has shown strong levels of growth over the last 3 years and they continue to develop their Regulatory franchise in a number of areas. 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)207 801 3380 -
Regulatory Affairs Specialist
Berkshire
Apr 1
Exciting opportunity with a global pharmaceutical company for a Regulatory Affairs Specialist - highly competitive package available!!
Senior Regulatory Affairs Specialist
Berkshire
Apr 1
Looking to advance your career? An exciting opportunity for a Senior Regulatory Affairs Specialist required for post marketing role - a permanent position with a global pharma company. Highly competitive salary offered!!
Regulatory Affairs (Principal) - Leading Global Pharmaceutical Company - £55k + Bonus + Benefits
Greater London and surrounding areas
Mar 31
We are currently sourcing for a Principal Regulatory Affairs Officer to join a Leading Global Pharmaceutical Company in the UK.
Regulatory Affairs Director Oncology – Take strategic leadership for Mid and late development and new EU and RoW submissions
Belgium, Brussels
Mar 31
If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, French and German speaking candidates should call Matt Grieg or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
Regulatory Affairs Senior CMC Manager – Biologicals – Close to Lausanne – Develop your expertise in MAbs and Global development projects
Lausanne
Mar 31
My rapidly expanding, and hugely successful Bio/pharmaceutical is expanding its global Biologicals CMC team which is based in Switzerland, close to Lausanne. If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above call Matt Grieg or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
Regulatory Affairs Snr Manager and Associate Director Roles - The Netherlands (close to Amsterdam) – Strategic roles for EU and Row markets
The Netherlands - close to Amsterdam
Mar 31
These roles come with a great salary, a full re-location package and the opportunity to work in a dynamic environment here there is a good atmosphere between colleagues and where people are always respectful and helpful. If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above all Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
Regulatory Affairs Contract - Early Phase Development Role - To £80 per hour for 12months - Maidenhead or Uxbridge
Maidenhead or Uxbridge
Mar 31
This role is a good mix of strategic input, Global project management and cover early and mid-phase development for biologicals and small molecules. 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)207 801 3380
Regulatory Affairs Manager
Uxbridge
Mar 31
PAREXEL UK is looking for experienced RA Manager with Line Management experience to join their Uxbridge team in the UK.
Regulatory Affairs Manager/Associate Director- Life Cycle Maintenance/CMC/Labelling - Permanent, Reading, UK
Reading, UK
Mar 31
Entrust Clinical People are actively resourcing for their Global CRO client for a Regulatory Affairs Manager or Associate Director, Regulatory Affairs. This is an exciting time to join a newly created team and work on a range of key projects within Regulatory Affairs, specifically on Product Life Cycle maintenance, Regulatory CMC and Labelling.
Regulatory Affairs (Associate Officer/Officer/Senior Officer) - Regulatory Life Cycle Maintenance/CMC/Labelling
Reading, UK
Mar 31
Entrust Clinical People are actively resourcing for their Global CRO client. This is an exciting time to join a newly created team and work on a range of key projects within Regulatory Affairs, specifically on Product Life Cycle maintenance, Regulatory CMC and Labelling.
Associate Corporate Regulatory Affairs (m/w)
Rhein-Main-Gebiet, Germany
Mar 31
Regulatory Affairs - Vollzeit - office based Rhein-Main-Gebiet - Sponsor
Senior Regulatory Affairs Manager - CMC - Germany-121359
France
Mar 27
PPD has a new vacancy for Senior Regulatory Affairs Manager. The ideal candidate will be an international regulatory CMC professional, and will be responsible for human pharmaceutical products, encompasses small and large molecules, injectable devices, investigational and marketed products, as assigned. ...
Principle Consultant Regulatory Affairs
Berkshire
Mar 26
Principle Consultant Regulatory Affairs - IDMPThe companyThis company is a top 5 global CRO with a large and ever growing consulting arm. This company is global company with over 10,000 employees across all continents. They are a company that help their clients get medicines into the hands of those who need them most. They offer scientific know how, industry expertise and an outstanding environment to learn and grow. ...
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