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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Regulatory CMC Senior Specialist, London
England
Sep 1
A fantastic opportunity to working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level.
Regulatory CMC Manager
England
Sep 1
Your primary function will be advising clients on strategic regulatory considerations for CMC product development, and be responsible for authoring and critically reviewing CMC sections of dossiers.
Regulatory Affairs Manager – Drug Development
Scotland
Sep 1
The main purpose of this role will be to define project and product regulatory strategy of the Development Group in line with commercial and company strategy, consulting with appropriate departments where necessary, to include: Representation of regulatory affairs at project team meetings for defined projects, providing information, feedback and strategic advice. Management of the regulatory activities associated with project team plans
Regulatory Project Manager
England
Sep 1
In the regulatory affairs franchise they provide innovative solutions including global regulatory therapeutic area expertise and to provide strategic regulatory intelligence, guidance and expertise.
Regulatory Project Manager – EU Locations, or Home Based
England
Sep 1
A fantastic opportunity has become available, working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level, this company invest heavily to attract and retain high quality staff; this organisation has a very credible reputation for being one of the best employees in its arena
Regulatory Affairs Manager - Established Products
England
Sep 1
A fantastic and immediate need has arisen at a global pharmaceutical company for a Regulatory Affairs Manager to join the team
Senior Project Manager/Regulatory Manager: Cambridge
Cambridge
Sep 1
A fantastic opportunity has become available, working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level, this company invest heavily to attract and retain high quality staff; this organisation has a very credible reputation for being one of the best employees in its arena.
Regulatory Affairs Manager
Surrey
Sep 1
Regulatory Affairs Manager Surrey, UK. Our client is a growing specialist healthcare company, working with pharmaceuticals and device technology and are looking for a Regulatory Affairs Manager to work within the Medical Devices division. This is an opportunity to help advise a team to work with some of the most cutting edge medical technologies on the market, and be part of a constantly growing and expanding company.
Regulatory Affairs Specialist
Germany
Sep 1
Regulatory Affairs Specialist Location: Freiburg area Clinical Professionals are working with one of the globe’s leading Devices companies to find a specialist with excellent experience in Regulatory Affairs to join their team in south-west Germany and aid in the development of exciting new Devices in conjunction with the US team.
Regulatory Affairs Manager \ Project Manager \ Regulatory Submissions Lead
East Anglia
Sep 1
Regulatory Affairs Manager \ Project Manager \ Regulatory Submissions Lead £50,000 - £65,000 – flexibility for highly experienced candidates Location: Flexible home working (can be entirely home based) or East Anglia Are you looking for a flexible company which allows you to be based from home? Are you interested in working for a forward thinking, innovative company?
Regulatory Affairs Associate \ Officer
Surrey
Sep 1
Regulatory Affairs Associate \ Officer Surrey Salary: up to £35,000 dependent upon experience. Do you have at least 6 months regulatory affairs experience? Would you like to work for a leading healthcare organisation that offer excellent training and development prospects?
Regulatory Affairs Officer\Regulatory Affairs Associate
Surrey
Sep 1
Regulatory Affairs Officer\Regulatory Affairs Associate Surrey •Do you want to work for an international Pharma Company? •Do you want to work for a company with cutting edge innovative Products?
Regulatory Affairs Submissions Manager / Regulatory Affairs Operations Manager
Ireland
Sep 1
Regulatory Affairs Submissions Manager / Regulatory Affairs Operations Manager Location: Ireland, East Coast. Salary: 80,000 - 100,000 Euros plus benefits. Our client will also offer a relocation package including 3 months rental property whilst you find your own place to live.My client a biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines is seeking a Regulatory Affairs Submissions Manager / Regulatory Affairs Operations Manager
EMEA Regulatory Liaison
Buckinghamshire
Sep 1
EMEA Regulatory Liaison: Buckinghamshire A fantastic opportunity has arisen for a Senior Regulatory Affairs Specialist with a leading pharmaceutical company. This is a contract position, office-based in Buckinghamshire. The aim for this role is to provide strategic and tactical input in development, post-approval and Life cycle management and EMEA liaison.
Medical Devices – Senior Regulatory Affairs Specialist
South East
Sep 1
Medical Devices – Senior Regulatory Affairs Specialist Office based (South East). Are you looking for an exciting opportunity to join an evolving company in a position which allows scope and progression?
Regulatory Affairs Manager – North West – Medical Devices
North West
Sep 1
Regulatory Affairs Manager – North West – Medical Devices Our client is an established ostomy and wound care medical devices specialist with over 6500 employees globally. Due to a change in structure they are now recruiting for a Regulatory Affairs Manager to be based within their North West office.
Senior Manager Regulatory Affairs
Netherlands
Sep 1
Senior Manager Regulatory Affairs Employment Type: Permanent Location: Netherlands A great opportunity has arisen for a Senior Manager within Regulatory affairs to join an established Medical Device company based in The Netherlands. This is a reputable company with strong presence not only across Europe but also the U.S.
Senior CMC Regulatory Director-Small Molecules Developmental
California
Sep 1
An experienced CMC professional with a background in small molecules is wanted to join my client, one of the leading pharmaceutical companies in California.
Senior Regulatory Affairs Specialist/ Medical Devices
Highland
Sep 1
A leading Medical Devices company is currently looking to hire a Senior Regulatory Affairs Specialist for a exiting new project based in Scotland. Job Description: * This role will support the RA project Leads for the new blood glucose monitoring system development projects. * Assisting in preparation of pre-market applications to regulatory agencies. ...
Senior Regulatory Consultant
London
Sep 1
A large global pharmaceutical company with leading products across various therapeutic areas are looking to hire a Senior Regulatory 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 with the possibility of an extension. ...
Regulatory Affairs Manager (m/w), Süddeutschland
München
Sep 1
Für ein internationales Pharmaunternehmen suche ich einen Regulatory Affairs Manager (w/m) für den Standort München. ...
Regulatory Specialist-Global Exposure-Netherlands
Netherlands
Sep 1
Regulatory Specialist-Global Exposure-NetherlandsA leading medical devices company are looking for two Regulatory Affairs Specialists to join their expanding team in Maastricht. You will be given exposure to a wide range of product portfolios across the world and be responsible for developing and coordinating international registration and documentation of Regulatory Affairs.
Head of Regulatory Licencing + Compliance
England
Sep 1
A very exciting opportunity for the Head of Licencing + Compliance.
Junior Regulatory Affairs Manager (m/w) in Magdeburg gesucht
Magdeburg
Aug 31
Junior Regulatory Affairs Manager (m/w)Arbeitsort: MagdeburgVertragsart: Unbefristete FestanstellungVertragsstart: SofortDie Medizintechnik-Junioren von heute sind die Fach- und Führungskräfte von morgen. Sie haben erste Erfahrungen im MedTech-Umfeld und sind interessiert daran, bei einem Global Player Karriere zu machen? Dann sind Sie der/die Richtige für uns!Ihre Aufgaben * Unterstützung von Medizinprodukte-Zulassungen in Europa, USA, Brasilien usw. ...
Broad Global Regulatory Affairs Associate position
London
Aug 31
Broad Regulatory Affairs Associate positionI currently have an interesting Regulatory Affairs associate opportunity available.
Top Pharmaunternehmen sucht Regulatory Affairs Manager (m/w)
Hessen
Aug 31
Für ein führendes Pharmaunternehmen im Raum Frankfurt suche ich einen Regulatory Affairs Manager (m/w) für die Durchführung von europäischen Verfahren. ...
Regulatory Affairs Manager (m/w) Raum Frankfurt
Frankfurt am Main
Aug 31
Für ein innovatives, mittelständisches Pharmaunternehmen mit tollem Betriebsklima suche ich derzeit einen Regulatory Affairs Manager (m/w). ...
Regulatory Specialists – Cosmetics – France
France
Aug 30
These exciting opportunities can offer you the position you've always wanted, from working with small or large companies to working with raw materials or finished products. Because I'm a specialist in this area, I understand your professional needs that allows me to find the best psotions that will advance your career and give you better job satisfaction.I can help you get your professional life to where you want to be!
Regulatory Toxicologist – Leading Consultancy – FR
Lyon
Aug 30
This is an exciting opportunity to join and agrochemical company that realises that people are the key to their future and will offer a mixture of on the job learning and professional training allowing you to keep your regulatory and technical knowledge as up to date as possible. They also realise that some people thrive when working independently so they have a home office option allowing you to manage your time efficiently.
Senior Regulatory Associate
Berkshire
Aug 29
Senior Regulatory Associate (12 month Contract)– BerskhireAn exciting opportunity for an experienced Regulatory professional with at least a couple of years’ experience to step into a fast paced and dynamic Pharmaceutical company. Join a strong development team focusing on Clinical Trial Applications and submitting them to the relative authoritative and ethical committees. ...
Global Regulatory/Quality Director-Medical Devices-Homebased
Berlin
Aug 29
Looking for a Global Leading Regulatory/Quality Position? Click Here...
Regulatory Affairs/Quality Assurance Manager - Medical Devices
Stuttgart
Aug 29
My client in the Stuttgart region, is currently offering a FANTASTIC opportunity for RA/QA professionals who are looking to develop their international experience in the medical devices industry.
Regulatory Specialist-Portfolio Responsibility-Netherlands
Netherlands
Aug 29
Regulatory Specialist-Portfolio Responsibility-NetherlandsA leading & continually expanding Medical Devices company working with a wide range of products on a global scale are seeking a Regulatory Affairs Specialist. Based in Limburg you will join a newly established team to drive regulatory strategy across the EMEA and eventually taking responsibility for your own product portfolio, a great way to gain visibility in the market.
Regulatory Specialist-Fast Moving Sales Environment-Netherlands
Netherlands
Aug 28
Regulatory Specialist-Fast Moving Sales Environment-NetherlandsA rapidly expanding Medical Devices company are looking for a Regulatory Affairs Specialist to join their team in their European Headquarters. You will have the opportunity to manage your own product portfolio throughout the entire regulatory cycle, ensuring the products are moved to market as soon as possible.
Regulatory Affairs Associate/ Senior Associate
Hampshire
Aug 28
Role: Regulatory Affairs Officer - Regulatory Affairs Senior OfficerSalary: Competitive - Depends on experienceLocation: South UK - (Hampshire) Want to join a company that specialises globally in the market for Ophthalmic Drugs? This company is looking to expand globally with licenses around ¾ of the world.
Regulatory Affairs Specialist - Hamburg - 55000€
Hamburg
Aug 28
Dies ist eine sehr interessante Rolle in einem starken Team, mit einem sehr attraktivem Gehalt und Bonus Packet. Falls Sie glauben das Sie gut in diese Rolle passen, dann senden Sie bitte Ihren Lebenslauf an Robert Marrett (mweber@optimussearch.com) und Wir können uns weiter über die Rolle unterhalten.
Regulatory Affairs Manager – Düsseldorf - €60,000
Düsseldorf
Aug 28
If you are interested in applying to this role, or even just to find out more details, please send a recent CV to mweber@optimussearch.com to arrange a call.
Regulatory Affairs Manager (Parallel Imports Specialist)
West London
Aug 28
Role: Regulatory Affairs Manager PLPI (Product Licence Parallel Import)Location: LondonSalary: Competitive Responsibilities:* Require detailed knowledge of the full licence application process for all the different Regulating Bodies and establish contacts/relationships with key people within these bodies.* Going through all correspondences from the governing boards and logging them in the appropriate databases and looking at the issues raised.
Senior Regulatory Affairs Manager – Duesseldorf – 60.000€
Düsseldorf
Aug 28
Sie haben die Chance in einem großen internationalem Pharma Unternehmen zusammen mit einem dynamischen Team zu arbeiten. Diese Arbeit ist sehr abwechslungsreich und sehr befriedigend. Falls Sie nun interresiert sind, melden Sie sich bitte bei mweber@optimussearch.com
Regulatory Writer - Module 2 focused
Paris
Aug 28
Regulatory Writer - Module 2 focusedI have a broad position in France currently; it could be a nice change for you in a English speaking international environment.
Senior Regulatory Consultant
London
Aug 28
A large global pharmaceutical company with leading products across various therapeutic areas are looking to hire a Senior Regulatory 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 with the possibility of an extension. ...
Regulatory Affairs Manager, EU
Basel
Aug 28
Regulatory Affairs Manager, EU, Partner Collaboration in Europe for Established Products
Regulatory Project Manager - IDMP - Home Based
Paris
Aug 28
I am working with a market leading Pharmaceutical Software company in the search for a Regulatory Information Project Manager with experience in the upcoming IDMP legislation implementation.
Regulatory Affairs Manager (m/w)
Hamburg
Aug 28
Regulatory Affairs Manager (m/w)Office-based near HamburgJob Description:- Writing/compilation and submission of market authorization applications- Regulatory maintenance activities of global approvals, including renewals- Develop regulatory strategies- Coordinate and respond to HA queries and deficiency letters- Maintaining and updating current SmPcs and PILs in cooperation with the relevant departments- Participation in Scientific Advice Meetings- Act as point of contact for health authori ...
Principle Regulatory Affairs Officer
Harlow, Essex, UK
Aug 28
My client, a top 10 global pharmaceutical company, are currently seeking a Principle Regulatory Affairs Officer to join their team in Essex, UK. If you have a number of years’ experience and are familiar with the respiratory therapeutic area then please read on and apply!
EU Regulatory Strategy Product Specialist
Farnborough
Aug 28
EU Regulatory Strategy Product Specialist - Pharmaceutical - UK - Competitive salary, bonus and benefits package.If you would like to apply for the position or wish to learn more about the role and company please call Mark on 0044 (0) 207 255 6665 or email your CV with a brief covering note to mark.wilkins@secpharma.com
clinical Regulatory specialist - Module 2
France
Aug 28
Non Stop is currently looking for a regulatory affairs specialist on behalf of a pharmaceutical group developing innovative diagnostic and therapeutic products in the field of Nuclear Medicine. As part of their development, your key tasks will be the following:
Senior Regulatory Affairs Specialist - experience of authoring documents , IMPDs , CTA work ,leading projects and post submission work with clients
Midlands
Aug 27
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 to discuss. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - International work - must have CTA experience
Cambridge
Aug 27
To apply for this regulatory affairs role please call Julie Cooper to discuss on 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - International work - must have CTA experience
Cambridge
Aug 27
To apply for this regulatory affairs role please call Julie Cooper to discuss on 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - ROW and EU submission work - Uxbridge with one day in Cambridge
Uxbridge or Cambridge
Aug 27
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - CMC - International work
Cambridge
Aug 27
To apply for this CMC Regulatory affairs role please call Julie Cooper on 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Associate -CMC - International
Cambridge
Aug 27
To apply for this regulatory affairs associate CMC please call Julie Cooper on 07951 082482 Alternatively please send your to me at :julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - ROW - Cambridge
Cambridge
Aug 27
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Consultant
Surrey
Aug 27
This Regulatory Affairs Consultant job is an excellent opportunity to work for a global leader in biopharmaceuticals located in the South East of England Surrey. The company has been established for more than 150 years and is a major supplier to the NHS. This is a 6 month contract with the possibility of an extension. ...
Senior Regulatory Affairs Officer
Scotland
Aug 27
The purpose of this role is to prepare, submit and maintain regulatory technical documentation, coordinate creation of product labelling, liaise with internal and external parties and provide regulatory support to the company.
Regulatory Affairs Spezialist – forschendes Unternehmen – Münch
Munich
Aug 27
Als Regulatory Affairs Spezialist arbeiten Sie an der Erstellung zulassungsrelevanter Dokumente für klinische Studien. So arbeiten Sie an Einreichung bei Ethikkommissionen und überprüfen die Dokumente. Weiterhin stellen sicher, dass die Studienzentren den regulatorischen Vorgaben entsprechen und diese richtig umgesetzt werden. Sie sind außerdem intern Ansprechpartner für regulatorische Fragen.
Regulatory Affairs Officer for leading Pharma in the North West
North West England
Aug 27
My client is a leading UK organisation who has grown significantly over the last century in an organic way with brands that have become household names. In this period of continued growth due to further acquisitions they now have a new permanent opening for a Regulatory affairs Officer to join their team based in the North West. This will give you the opportunity to develop your hands-on regulatory experience in submissions and communicating with Health Authorities.
Associate regulatory Affairs Officer - Recent graduate with biological / life science degree- some experience of writing ethic submissions
Midlands
Aug 26
To apply for this regulatory affairs role you will need to call Julie Cooper on 07951 082482 or email me on julie@mosaicrecruitment.co.uk
UK Regulatory Affairs Director
London
Aug 26
UK Regulatory Affairs Director - Permanent - Office or Home based - CRO - £100,000+ salaryIf you would like to apply for the position or wish to learn more about the role and company please call Mark on 0044 (0) 207 255 6665 or email your CV with a brief covering note to mark.wilkins@secpharma.com
Regulatory Affairs Manager, Technical Focus
Basel
Aug 26
Regulatory Affairs Manager, Drug development, CMC, Basel area, Opportunity to work with complex molecules
Regulatory Affairs Manager - Develop A Pharma Division
Berkshire
Aug 26
Regulatory Affairs Manager - Develop A Pharma DivisionI am looking for a Regulatory Affairs manager to develop the pharma division of a leading OTC company.
VP, Head of Regulatory Affairs - EU
South East
Aug 26
Skills Alliance is delighted to announce an exclusive partnership with an emerging US biopharma company who are in the process of establishing their European Headquarters...
Regulatory Affairs Manager/Specialist
South East England
Aug 26
A very exciting role as a Regulatory Affairs Manager has just become available for a rapidly growing pharmaceutical & nutritional supplement manufacturer based in Hertfordshire. You will be responsible for reviewing and approval of Food Supplement for the UK and Ireland. The Regulatory Affairs Manager provides close and active support to the Technical, Marketing and Sales teams in the UK and Ireland & EU.
Regulatory Labelling Manager
Surrey
Aug 26
This Regulatory Labelling Manager job is an excellent opportunity to work for a global leader in biopharmaceuticals located in South East of England in Surrey. The company has been established for more than 150 years and is a major supplier to the NHS. This is a 12 month contract role with the possibility of an extension. ...
Regulatory Affairs Senior Manager - London
London
Aug 26
Senior Regulatory Manager to be based in London.
Senior Regulatory Affairs Associate - ROW - Cambridge
Cambridge
Aug 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 Specialist - CMC - Move to amazing company in leafy surroundings - Nottinghamshire
Midlands
Aug 26
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 to discuss. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Specialist - experience of authoring CMC documents , CTA work ,leading projects -Midlands
Midlands
Aug 26
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 to discuss. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Associate regulatory Affairs Officer - Midlands - CTA and Ethics work - will consider 3 months of this experience or some experience in CRO
Midlands
Aug 26
To apply for this regulatory affairs role you will need to call Julie Cooper on 07951 082482 or email me on julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Specialist - experience of authoring documents , IMPDs , CTA work ,leading projects and post submission work with clients
Midlands
Aug 26
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 to discuss. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Expert, Berlin
Berlin
Aug 26
* You have at least 5-8 years’ experience in the area of regulatory affairs and you would like to work for an innovative German pharmaceutical company? * You have international experience? * You would like to work for a market leading company that offers exciting career prospects?Then I have a fantastic opportunity for you at a pharmaceutical company in Berlin!In this position you will have the following responsibilities:You will… * oversee the entire regulatory process, including new regis ...
Regulatory Affairs CMC Senior Manager - Cambridge.
England
Aug 26
I am looking for a fantastic Senior Regulatory Manager with a focus in CMC and 10 years experience working in Cambridge.
Regulatory Toxicologist – Career Progression - France/England
Avignon
Aug 26
This is a fantastic opportunity for a young regulatory toxicologist who wants to work in a friendly environment where they will receive technical training and encourage to attend industry seminars. This coupled with on the job learning from colleagues and client companies will enhance your professional skillset making you a more valuable asset to the company.
EU Regulatory Affairs Program Manager Pediatric Oncology
Switzerland
Aug 26
The program manager position will cover pediatric and adult programs in hematological malignancies and be responsible for the regulatory strategic and operational management. The role will report to the regulatory iPODD (innovative Pediatric Oncology Drug Development) franchise head. ...
Regulatory Operations Associate
Hertfordshire
Aug 25
Regulatory Operations AssociateFantastic opportunity to join a successful OTC Medicinal company, involved with life changing medication. Unique opportunity to work with this company on a contract basis for initially 6 months.Responsible for the assembly and/or review of electronic and paper submission applications, publishing, production, dispatch, logging and archiving for regulatory submissions and/or notifications. ...
Regulatory Submission Manager - top CRO - Hungary
Hungary
Aug 25
We are currently seeking for an energetic and motivated Regulatory Submission Manager to join our clinical team in Hungary and manage European-wide clinical trial application submissions on a permanent basis In this sounds appealing to you, please contact Aine Uusvel from Meet via email aine@peoplewithchemistry.com or via phone +44 789 650 6004. The applications will be handled with discretion.
Senior Regulatory Affairs Specialist -regulatory lead - experience of authoring CMC documents , IMPDs , CTA work
Midlands
Aug 25
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 to discuss. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Associate regulatory Affairs Officer - Midlands- Ethics and CTA work - must have have some experience of working in similiar environment- 2-3 months
Midlands
Aug 25
To apply for this regulatory affairs role you will need to call Julie Cooper on 07951 082482 or email me on julie@mosaicrecruitment.co.uk
Regulatory Compliance Manager – Small Company – Germany
Germany
Aug 25
As Regulatory Compliance Manager you will be responsible for overseeing the compliance of the regulatory submission documents with regulatory guidelines. You will do this for new submissions, variations and renewals and for EU and global projects. You are in touch with regulatory authorities and answer any questions they may have. Further, you make sure that project dates will be adhered to and that submissions are finished on time.
Regulatory Manager - Full lifecycle - NRW, Germany
Aachen
Aug 25
Apply now for a very interesting position in Regulatory Affairs for a globally renowned company in Germany. The role will involve performing project and full lifecycle management, with a particular focus on Germany and the wider DACH region. It will give you an opportunity to in the future develop and work in the headquarters of the company, thereby gaining an international scope. ...
Senior Regulatory Affairs Associate - International work - must have CTA experience
Cambridge
Aug 25
To apply for this regulatory affairs role please call Julie Cooper to discuss on 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - ROW and EU submission work - Uxbridge with one day in Cambridge
Uxbridge or Cambridge
Aug 25
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Associate -CMC - International
Cambridge
Aug 25
To apply for this regulatory affairs associate CMC please call Julie Cooper on 07951 082482 Alternatively please send your to me at :julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - ROW - Cambridge
Cambridge
Aug 25
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 Specialist - CMC - Midlands
Midlands
Aug 25
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 to discuss. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Specialist - experience of authoring documents , CMC writing - Midlands
Midlands
Aug 25
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 to discuss. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Specialist - Regulatory Lead, write CMC sections, compile and submit CTAs to MHRA.
Midlands
Aug 25
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 to discuss. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Professional EMEA
Buckinghamshire
Aug 25
Oliver Care at CK Clinical is recruiting for a Senior Regulatory Professional for the EMEA to join a company in the pharmaceutical industry at their...
Regulatory Operations Assistant
Cambridge
Aug 25
An exciting opportunity has arisen for a Regulatory Operations Assistant job at a global biopharmaceutical company based in Cambridge, UK. The company is highly patient-focussed with marketed products that are benefitting hundreds of thousands of people, a pipeline of late-stage drug candidates and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. ...
Regulatory Affairs Manager - Regulatory Development
Edinburgh
Aug 25
I am urgently searching for a regulatory professional to work for a rapidly growing speciality pharmaceutical company based near Edinburgh.
Regulatory Affairs Director
North Holland
Aug 25
Head of Regulatory Affairs For an organization, located in the Randstad, I am looking for a Head of Regulatory Affairs. Job DescriptionIn this role you will be responsible for the management and supervision of Regulatory Affairs for the national and international department in line with global and regional strategies and compliance requirements. You support the local RA unit in submissions and regulatory compliance for the organizations portfolio. ...
Regulatory Associate Director
England
Aug 25
Client is a leading global contract research organization supporting their clients from clinical & drug discovery stages. Ideal candidate needs strong development and CTA experience, late stage clinical experience a proactive style and the ability to use initiative.
Senior Associate – Regulatory Publishing, EMEA
Buckinghamshire
Aug 25
A leading organization in Buckinghamshire is looking for an experienced regulatory publisher to join them in the role of a senior associate for EMEA regions.
Quality and Regulatory Specialist-Dedicated QandR Team-Belgium
Brussels
Aug 25
Quality & Regulatory Specialist-Dedicated Q&R Team-BelgiumI am looking for an experienced Q&R professional to join a long standing, global leader in the dental industry. By joining a dedicated team of like minded professionals you will continue to strengthen your knowledge and ultimately your profile, enhancing your exposure and future opportunities.
Regulatory affairs specialist - Clinical - English
France
Aug 25
Non Stop is currently looking for a regulatory affairs specialist on behalf of a pharmaceutical group developing innovative diagnostic and therapeutic products in the field of Nuclear Medicine. As part of their development, your key tasks will be the following:
Regulatory Affairs Manager
Galway
Aug 25
Regulatory Affairs Manager Job Description Due to their current expansion, an exciting opportunity has arisen for a Regulatory Affairs Manager to join a well recognised International Pharmaceutical company. You will be working on both submissions and lifecycle activities for assigned products within your portfolio.Key Duties * Responsible for the implementation of registration strategy for a number of projects ensuring the regulatory approval of successful products. ...
Regulatory Manager - Interim Contract
and Home-Based
Aug 24
Regulatory affairs, cmc, lcm. labelling, post-market, cta, manager, project manager, compliance, global, EU, remote working, Germany
Associate regulatory Affairs Officer - Midlands - writing and managing ethics submissions for clinical trials- 3- 6 months experience
Midlands
Aug 24
To apply for this regulatory affairs role you will need to call Julie Cooper on 07951 082482 or email me on julie@mosaicrecruitment.co.uk
Associate regulatory Affairs Officer - Midlands- will consider fresh graduate with biologics background and CTA understanding as part of placemet
Midlands
Aug 24
To apply for this regulatory affairs role you will need to call Julie Cooper on 07951 082482 or email me on julie@mosaicrecruitment.co.uk
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