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Principle Regulatory Writer - Home Based – UK - £70,000 + car + bonus
Home based, UK
Jun 22
We are a leading pharmaceutical company looking for a Principle Medical Writer to join our global team and support in a home-based capacity supporting our oncology business. The ideal candidate would have worked with a broad range of clinical documents and have submissions experience.  
Regulatory Affairs Manager (m/w)
Switzerland
Jun 22
Regulatory Affairs Manager (m/w)Office-based in St.Gallen Vollzeit- unbefristet Für einen sympathischen Kunden der Medizintechnik -Branche in der Herstellung von dentalen Produkten sind wir auf der Suche nach einem Regulatory Affairs Manager. ...
Regulatory Affairs CMC Manager
Basel
Jun 22
Regulatory Affairs CMC Manager wanted for our Basel based client in the pharmaceutical sector.Your experience/skills: * Degree in Science, e.g. ...
Regulatory Affairs CMC Manager
Germany
Jun 22
Für unseren Kunden sind wir aktuell auf der Suche nach einem Regulatory Affairs CMC Manager (m/w). ...
Regulatory Affairs Officer - work on MAAs , post approval and all aspects of regulatory work
Oxfordshire
Jun 22
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - International role- Cosmetics
Nottingham
Jun 22
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482. Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Global CMC Regulatory Affairs Manager - Midlands
Midlands
Jun 22
To apply for this CMC Regulatory Affairs Manager please call Julie Cooper on 07951 082482 to discuss this role. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Global Principal Regulatory Specialist - Galway
Galway
Jun 22
Just Pharma are currently working with Global Medical Devices company who are searching for a Principal Specialist to join their Global Regulatory Affairs Team. The Principal Regulatory Specialist will be responsible for working with Class II Medical Devices that are new to the company following acquisition and licensing agreements. ...
Regulatory Specialist- Contract
West Yorkshire
Jun 22
This Medical Device client is looking for a Regulatory Specialist to help support with the EUMDRStart ASAP12-18 monthsRate: TBC40 hours across 5 daysLocated in West YorkshireTo provide assistance in preparation and submission of global regulatory documents under little or no supervision.
Senior Regulatory CMC Consultant
Uxbridge
Jun 22
ProClinical is currently recruiting for a regulatory affairs job on behalf of a top 10 global pharmaceutical company located in Uxbridge on a contract basis.Job Responsibilties: * Preparation of high quality, Chemistry, Manufacturing and Control (CMC) detailed regulatory documents using varied information sources. liaising closely with other company personnel to ensure accuracy of such records. ...
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Regulatory Affairs Director - Emerging Markets
Cambridge
Jun 22
A well-known global pharmaceutical company with leading products across various therapeutic areas is looking to hire a Regulatory Affairs Director - Emerging Markets. This vacancy is an exciting opportunity to work at a top global pharmaceutical company that has a workforce of more than 6,700 employees across multiple sites in the UK. ...
Regulatory Affairs CMC Associate Manager
Basel
Jun 22
Regulatory Affairs CMC Associate Manager with profound Basel knowledge wanted for our Basel based client in the pharmaceutical sector. ...
Senior Regulatory Specialist - Clinical Trials
England
Jun 22
A rare opportunity as a Senior Regulatory Specialist at a global CRO has recently emerged. If you are looking for a new opportunity to broaden your scope of work, and further your career get in touch immediately. In your role as Senior Regulatory Specialist, you will be joining their late phase team in one of their excellent European locations. The company in question will enable you to work with professionals dedicated to improving the lives of thousands.
Regulatory Affairs Officer
United Kingdom Frimley / Camberley
Jun 22
Regulatory Affairs Officer, Alcon, UKJob Summary:Would you like to work for Alcon Inc., the world’s leading eye care company dedicated to the provision of not only the highest quality eye care products but to also making significant contributions towards prevention and elimination blindness?We foster the professional growth of our associates by providing ongoing opportunities that can build upon their knowledge and skills to help further their careers. ...
Senior Regulatory Affairs Manager, CMC
Cambridgeshire
Jun 21
Regulatory Professionals are collaborating with a global bio-pharmaceutical company with a strong pipeline including treatments for cancer, HIV and respiratory diseases.
Senior Regulatory Affairs Associate
Slough
Jun 21
ProClinical is seeking a Senior Regulatory Affairs Associate to be based in Slough on a permanent basis. This role will manage clinical trial applications of new and established pharmaceuticals performed at or by the company, ensuring that applications are conducted in accordance with the latest ICH and Regulatory Affairs guidelines. ...
Regulatory and Start-up Specialist
Stockholm
Jun 21
ProClinical is working with a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. This CRO is seeking a Regulatory start-up specialist to be based in Sweden on a permanent basis.This CRO's European activities are growing rapidly, and are currently seeking a full-time, home-based Regulatory Submissions Coordinator to join their Clinical Operations team. ...
Regulatory Affairs - Medical Device - Switzerland
Basel
Jun 21
Jocelyn Blackham is recruiting for a number of Regulatory Affairs Specialists who have expert knowledge within the Medical Device area. The successful candidates will be...
Regulatory Affairs Specialist - Switzerland
Switzerland
Jun 21
Mary Bolt is recruiting for a Regulatory Affairs Specialist to be based with a well known, global healthcare company with a varied portfolio of Medical...
Regulatory and Site Services Specialist (M/W)
Based in Bad Homburg
Jun 21
We are looking to recruit Regulatory and Site Services Specialist About the department: This department provides an efficient, quality-centric approach to study startup activities with a growing focus on site relationships.
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Regulatory Affairs Specialist - Oberdorf, Switzerland
Oberdorf B L
Jun 21
Jocelyn Blackham is recruiting for a Regulatory Affairs Specialist to join a global organisation, specialising in the development of medical devices at their site based...
Regulatory Affairs Specialist Medical Devices
Paris
Jun 21
4 X Regulatory Affairs Specialist Medical Devices - France/Paris Are you interested in working with a friend or colleague? We are looking for 4 X Regulatory Affairs Specialist Medical Devices! This role is based out just outside of Paris for a Medical Device company to which you will be working on a international project. This company is going through a massive restructuring and require intensive support. ...
Regulatory Affairs Director - Emerging Markets
Cambridgeshire
Jun 20
This leading pharmaceutical firm is currently collaborating with Regulatory Professionals, recruiting for a Regulatory Affairs Director within Emerging Markets on a 12 month contract basis.
Regulatory Ad Promo Specialists / Experts – Ad Prom incl. Digi and Traditional Media for a high performing franchise
Georgia
Jun 20
This is not your normal type Ad Prom role, as my client has invested heavily in developing and fine tuning a new way of working for our client organization’s Regulatory Ad Prom folks, by bringing critical review to the beginning of the creative process, and repositioning the role, with an emphasis on partnering in the creative process from the start ...
Regulatory Affairs Team Leader Pre-Clinical (m/w)
Germany
Jun 20
Für unseren Kunden aus Süddeutschland suche ich nach einem Team Leader für die Dokumentation Abteilung der Regulatory Affairs in der präklinischer Phase. Sie bekommen klare Entwicklungsmöglichkeiten und ein attraktives Bonussystem in Verbindung mit einem Awardwinning Work-Life Balance. ...
Regulatory Affairs Director
Cambridgeshire
Jun 20
If you are inspired by developing your career in a stimulating environment where you can make a profound difference to the healthcare of patients.
Senior Regulatory Executive x 2 - Uxbridge
Uxbridge
Jun 20
CK Group is recruiting for a Senior Regulatory Executive to join a company in the Pharmaceutical industry at their site based in Uxbridge on a...
Head of Regulatory Affairs
Netherlands
Jun 20
Head of Regulatory Affairs, Netherlands International organisation is looking for a Head of RA to join their RA department in Netherlands. ...
Regulatory Affairs Manager – Global Clinical Supplies and Regulatory Affairs (CMC), Athlone-146718
Europe, Middle East and Africa-Ireland
Jun 20
PPD has a new position available for a Regulatory Affairs Manager to join our Regulatory Affairs department.  This is a fantastic opportunity to advance your regulatory career in an exciting and fast paced environment.    This position is to be based in PPD Athlone. In this role, you will support the Global Clinical Supplies (GCS) function and Regulatory Affairs (CMC) to provide regulatory and quality advice, and carry out projects in the provision of regulatory affairs services. ...
Regulatory Affairs Manager - Exciting Global Biopharma, Sussex/South England – upto £70,000 + Bonus + Benefits
West Sussex
Jun 19
We are a growing Global Biopharma going through an exciting period of growth and we are now recruiting for an experienced Regulatory Affairs Manager to champion change, provide full oversight of the regulatory function, work on international projects and lead a team of regulatory professionals. This is a really exciting opportunity offering excellent career development and work-life balance.
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Regulatory Affairs Specialist
Limerick
Jun 19
Regulatory Affairs Specialist required for global medical device company!
Regulatory Trainees for Labelling and Advertising and Promo - Real career opportunity - Develop and build your experience...
Atlanta, Georgia
Jun 19
You might have completed a Master’s degree in Regulatory Sciences, or have gained industrial training and rotation experiences in regulatory department as part of or after your degree, and now would like a settled position, where you can master the theory into practical experience. Call Theo Moore or Matt Greig  Toll Free from the US on 855 505 1382.
Academy SSU and Regulatory Specialist
farnborough
Jun 19
Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
Regulatory Site Activation Manager
Flexible Location
Jun 19
Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
Senior Regulatory Affairs Associate
Berkshire
Jun 19
Regulatory Professionals are collaborating with an established CRO based in Berkshire who specialise in oncology and rare diseases.
Regulatory Affairs Associate II
England
Jun 19
Our Client, a global bio pharmaceutical company are seeking a Regulatory Affairs Associate II to join their RoW Markets team in their U.K. Facility.The Position As a Regulatory Affairs Associate II, you will be joining their Rest of The World market team and providing support to the organisations markets outside of the E.U and the U.S. ...
Senior Regulatory Affairs Associate
England
Jun 18
Our Client, a global bio pharmaceutical company are seeking a Senior Regulatory Affairs Associate to join their U.K. facility to work as a country liaison for rest of the world team.The Position As a Senior Regulatory Affairs Associate, you will provide support to the organisations activities in Latin America and the Caribbean. You will maintain the organisations existing licenses and support new licence applications, variations PSURs/RMPs, responses to questions and renewals. ...
Regulatory Affairs Manager
England
Jun 18
Our Client, a global bio pharmaceutical company are seeking a Regulatory Affairs Manager to join their U.K. facility to lead, define and implement the international Regulatory department and Regulatory strategy.The Position As the Regulatory Manager, you will be reporting into the Senior Director of Regulatory Affairs and rapidly expanding their regulatory intelligence foundations. ...
Senior Regulatory Affairs Associate - Lancashire
Lancashire
Jun 18
Mary Bolt is recruiting for a Senior Regulatory Affairs Associate- Medical Devices to join the Medical Device business of a highly established global healthcare company...
Contractor Regulatory Affairs, Oncology - Hertfordshire
Hertfordshire
Jun 18
Mary Bolt is recruiting for a Contractor Regulatory Affairs - Oncology to join a global pharmaceutical company committed to contributing to better healthcare at their site...
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Senior Manager Regulatory Affairs - Oncology - Hertfordshire
Hertfordshire
Jun 18
Mary Bolt is recruiting for a Senior Manager Regulatory Affairs - Oncology to join a global pharmaceutical company committed to contributing to better healthcare at their...
Regulatory Labeling Project Manager
Surrey
Jun 18
Our client, a top 10 global pharmaceutical company who offer medicines and vaccines across a broad range of therapeutic areas with the view to save lives, prevent sickness and improve health.
Regulatory Affairs Associate (temporary contract)
Moscow, Moscow,Russia
Jun 16
The role is a maternity leave replacement (1.5 - 3 years) Role context:As part of a multi-national project team, you will take the lead to coordinate the compilation, review and submission of regulatory agency applications for international clinical trials in compliance with international regulatory requirements as well as internal and client standard operating procedures (SOPs). ...
Regulatory Affairs Snr Manager - Join a dynamic Biotech with a great pipeline offering training to become a GRL - Brussels
Belgium
Jun 15
With their focus on natural, long-term growth, this amazing organisation depends on the contributions of talented and committed professionals like you who are determined to drive through progress. In turn, they make sure your work environment leaves you the space you need to attend to your personal goals, meet your family obligations, and pursue your professional development. Contact Theo Moore or Matt Greig NOW on +44 207 801 3384 or email us via CV@AdvRegualtory.com
Regulatory Affairs Director (Early Phase Global Development)
UK, M4 Corridor
Jun 15
You will work on US and EU as well as AP INDs, from regulatory strategy documents which you will co-author. The role is focused on early stage molecules, supporting 4 or so groups of indications, in a company where R&D is mostly based in Europe. A car allowance, bonus and stock plan are on offer for this role. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Policy and Intelligence Director UK W London or M4 OR 2/3 different EU locations
UK, M4 Corridor
Jun 15
NEW ROLE *** Regulatory Policy & Intelligence Director or Associate Director, Reg Policy & Intell We have 2 possibly 3 European locations open for this position, including the UK M4 Corridor area, and either French speaking, German or Dutch location. My client is a well-known, global, drug development company with a strong foothold in their chosen therapy areas and with a global objective ... >>> click to read on >>>
Regulatory Affairs Director - Lead Regulatory Policy for EMEA
UK, South-East
Jun 15
Would you consider a new opportunity if it gave you the chance to drive and shape policy across the entire development portfolio of Biologicals in a highly visible and influential role? This is highly visible and influential role, which would suit someone looking for a big challenge with a quickly developing and growing organisation. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Site Start-Up and Regulatory Specialist II (Warsaw)
Poland
Jun 15
Syneos Health is looking for an experienced Site Start-up & Regulatory Specialist II based in Warsaw.
Team Director Regulatory CMC Biologicals (mAbs) Based in 1 of 3 UK or EU Locations Big team, decent pipeline, great people
UK, CH or Europe
Jun 15
You will have a strong track record in regulatory strategy leadership for CMC for biologicals and some team management either full line or fuller matrix, and want to take on more of a people leadership role, in a company where behaviours and success factors, are important mantras in management roles.
Regulatory Associate - Ulverston
Ulverston
Jun 15
CK Group is recruiting for a Regulatory Associate to join a company in the pharmaceutical industry at their site based in Ulverston to work part...
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Regulatory Affairs Officer 2 - Office based, Reading, UK
Reading
Jun 15
PURPOSEPrepares and/or reviews regulatory submissions to support clinical trial and marketing authorisation activities for either internal and/or external clients. With guidance from senior staff, provides regulatory support for more complex projects.RESPONSIBILITIESActs as a Regulatory Team Leader on more complex projects, which may include technical writing.Prepares and/or reviews regulatory documentation in area of expertise, as appropriate. ...
Associate Regulatory Affairs Director - Labelling Expertise - Office based, Reading, UK
Reading
Jun 15
PURPOSEDirect, oversee and manage complex regulatory projects, ensuring quality deliverables on time and within budget. Ensure that all project work is completed in accordance with SOPs, policies and practices.RESPONSIBILITIESMay act as a Project Manager for a large stand-alone programme, involving several regulatory or technical deliverablesand/or region, and/or operation. Undertakes risk analysis, management and contingency plans, as appropriate. ...
Regulatory Affairs Specialist Freelance 6 Months
Germany
Jun 15
Sie würden den Aktualisierungsprozess des Zulassungsdossier der aktuellen gesetzlichen Anforderungen und Richtlinien in Deutschland unterstützen. Die Arbeit beinhaltet die Planung, Erstellung und Bewertung von Dokumenten und die Kooperation mit den Produktions- und Qualitätseinheiten. ...
Part-Time Regulatory Associate - Weybridge
Weybridge
Jun 15
CK Group is recruiting for a Part Time Regulatory Associate to join a company in the pharmaceutical industry at their site based in Weybridge on...
Regulatory Affairs Manager, £60-70k, Oxford, Medical Devices
Oxford, Reading, Newbury, Swindon
Jun 15
Are you looking for your next exciting challenge working for an international organisation? I am working on a fantastic opportunity in the Oxford area enabling you to become an integral part of the team and excel your career. This start-up medical device company are using world leading research to implement great changes within the industry resulting in improved patient outcomes.
Senior Regulatory Affairs Associate
Cambridgeshire
Jun 14
This internationally recognised bio-pharmaceutical company are presently collaborating with Regulatory Professionals, seeking an experienced Senior Regulatory Associate.
Teamleader Regulatory Affairs (m/w) Early Development
Baden-Württemberg
Jun 14
Teamlead (m/w) Regulatory Affairs, Early DevelopmentBaden-Württemberg / Vollzeit, office basedIhre Aufgaben:- Übernahme der Funktion als Teamleiter für zwei Teams für die Erstellung von regulatorischer Dokumentation für die frühe Entwicklung (Präklinik/Klinik/Toxikologie)- Aufbau neuer regulatorischer Prozesse und SOPs, sowie die Mitgestaltung der Funktionen innerhalb des Teams- Kontaktpflege zu Behörden, externen Dienstleistern und internen Abteilungen – insbesondere Regulatory Affairs & Ph ...
Regulatory Submissions Specialist
Maidenhead
Jun 14
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Submissions Contractor- on an initial 12 Month basis to be based at there offices in Berkshire.
Regulatory Affairs Director
Cambridgeshire
Jun 14
Regulatory Professionals are working exclusively with a global biopharmaceutical company who are continuing to drive the development of therapeutic human antibodies.
Regulatory Affairs Specialist- Labelling, Bulgaria-146974
Europe, Middle East and Africa-Bulgaria-Sofia-Sofia
Jun 14
PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...
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Regulatory Affairs Specialist, Bulgaria-146997
Europe, Middle East and Africa-Bulgaria-Sofia-Sofia
Jun 14
PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...
Senior Regulatory Affairs Manager CMC
Cambridgeshire
Jun 13
Regulatory Professionals are working with a leading International pharmaceutical company who are looking for Senior Regulatory Manager CMC.
Senior Regulatory affairs specialist
Paris
Jun 13
Senior Regulatory Affairs SpecialistIle de France - CDIDescription: * Prépare les dossiers de variations (CMC et labeling) en lien avec l'ERMC et l'international * Suivi des dossiers auprès des autorités de santé * Activité d'implémentation des modifications AMM * Traductions des annexes * Contrôles des BAT des articles de conditionnement * Assurer la bonne qualification des documents de communication transmis par les équipes internes et assurer leur conformité réglementaire * Veiller les ch ...
Assistant to Regulatory Department
Warsaw, Masovian Voivodeship,Poland
Jun 13
Main responsibilities:Provide administrative support, ensuring efficient operation of the office or function.Primary duties include office management, assisting with reports, project deliverables, phone coverage, maintenance and upgrades of office equipment, electronic file management, copying, filing and general typing. ...
Regulatory Affairs Specialist
Singapore
Jun 13
* REGULATORY AFFAIRS SPECIALIST- SINGAPOREJOB TITLERegulatory Affairs Specialist LOCATIONOffice Based in Singapore BENEFITS * Competitive salary * Personal and company performance related bonuses * Full corporate benefits package ROLE/DESCRIPTION * Oversee registrations and submissions of diagnostic devices in the Asia Pac region * Be involved in clinical trials and evaluations for blood cancer * Interpret and analyze complex data * Liaise directly with international regulatory agencies; han ...
Regulatory Compliance Coordinator
Rep. Ireland
Jun 12
On behalf of my client, a specialist healthcare provider, I have an exciting opportunity available for a Regulatory Compliance Coordinator. This is a permanent role within the company’s Dublin facility, reporting directly to the Operation Manager. If you are a highly motivated, ambitious and dedicated individual with Regulatory / Compliance experience in the Medical Device sector, we would like to hear from you!
Regulatory Affairs Consultant
Hertfordshire
Jun 12
This internationally recognised Japanese pharmaceutical firm seeks an experienced contract Regulatory Consultant to work within their dynamic oncology department on a 12 month contract basis.
Regulatory Affairs Associate - Czech Republic
Prague
Jun 12
An exciting opportunity at PRA in Czech Republic to join our team as a Regulatory Affairs Associate and work for an award winning CRO.
Manager (m/w) Regulatory Affairs
Berlin
Jun 12
Manager (m/w) Regulatory AffairsBerlin / Vollzeit, office basedIhre Aufgaben:- Übernahme der Funktion als Informationsbeauftragten nach § 74a AMG- Management aller laufenden Zulassungen, inklusive deren Aufrechthaltung sowie durch Einreichung von Variations, Renewals und Changes/Change Control- Aufbau neuer regulatorischer Prozesse und SOPs, sowie die Mitgestaltung der Funktionen innerhalb des TeamsWas Sie mitbringen sollten:- Naturwissenschaftlicher Hochschulabschluss, vorzugsweise Biologie ...
Regulatory Affairs Manager (m/w) FMD
Germany
Jun 12
Eine Abwechslung zu den meisten Regulatory Affairs Projekten. Für die neuen Falsified Medicines Directives Anforderungen braucht unserer Kunde Unterstützung für die nächsten 9 Monate in Vollzeit. Als weiteres werden Sie sich auf den Einfluss von Brexit auf den Kundenportfolio fokussieren. ...
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Head of European Regulatory Strategy / OTC/Consumer Care / Cambridge
Cambridge
Jun 12
Head of Regulatory Strategy; Leadership of the European Regulatory Team; OTC/Consumer Products; Development, new Registrations and Post approval; Cambridge location
Regulatory Consultant- FMD 3 Days a week
Uxbridge
Jun 12
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a part time Regulatory Affairs Consultant with experience dealing with EU FMD to be based at their offices in West London.
Quality and Regulatory Affairs Manager
Sweden
Jun 12
Quality and Regulatory Affairs Manager * Job type: Permanent * Location: Sweden, Malmo * Salary: 60000-70000.kr per monthSwedish Pharmaceutical and Medical Device Company are looking to hire a Quality Assurance and Regulatory Affairs Manager to lead their Regulatory Affairs Department at their State of Art facilities in Malmo, Sweden. ...
Senior Regulatory Associate ROW
Cambridgeshire
Jun 11
Regulatory Professionals are collaborating with a global bio-pharmaceutical company with a strong pipeline including treatments for cancer, HIV and respiratory diseases.
Regulatory Affairs Officer
Surrey
Jun 11
Regulatory Professionals are working with an ever-growing global Healthcare Company who are seeking a talented Regulatory Affairs Officer to join their Consumer Healthcare team.
Regulatory Affairs Associate II
Cambridgeshire
Jun 11
Regulatory Professionals are collaborating with a global bio-pharmaceutical company with a strong pipeline including treatments for cancer, HIV and respiratory diseases.
Site Activation and Regulatory Strategist
Europe - Other
Jun 11
Responsible for developing a robust global site activation and regulatory strategy for assigned projects including identification of regulatory risks and potential mitigations.  Supports the sales process by translating the regulatory strategy into compelling proposal text and representing the Site Activation team at Bid Defense Meetings.  Serves as an expert resource for other members of the Site Activation department to ensure appropriate execution of the developed global regulatory strategy.
Regulatory Affairs Associate
Maidenhead
Jun 11
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Affairs Associate - on an initial 6 Month contract to be based at there offices in Berkshire.
Regulatory Affairs Specialist - Medical Device
Lausanne
Jun 11
ProClinical is working with a Global Medical Devices company that is looking for Regulatory Affairs Specialist to support Life cycle management activities.Job Responsibilities: * Senior regulatory/clinical professional with specialized expertise in the regulation and clinical development of medical devices in European markets. ...
Director/Senior Director, Regulatory Affairs - Business Unit Lead-145060
Europe, Middle East and Africa
Jun 11
Director/Senior Director, Regulatory Affairs – Functional Service Solutions PPD has available an exciting new career opportunity for a Director/Senior Director Regulatory Affairs and head of Regulatory Affairs Functional Services Solutions team.  This is a senior level role working closely with the Regulatory Affairs leadership team, leading our Functional Services Solutions business unit. ...
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Regulatory Affairs Snr Manager - Join a dynamic Biotech with a great pipeline offering training to become a GRL - Brussels
Belgium
Jun 11
With their focus on natural, long-term growth, this amazing organisation depends on the contributions of talented and committed professionals like you who are determined to drive through progress. In turn, they make sure your work environment leaves you the space you need to attend to your personal goals, meet your family obligations, and pursue your professional development. Contact Theo Moore or Matt Greig NOW on +44 207 801 3384 or email us via CV@AdvRegualtory.com
Regulatory Affairs Manager - International role- Cosmetics
Nottingham
Jun 8
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482. Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Global CMC Regulatory Affairs Manager - Midlands
Midlands
Jun 8
To apply for this CMC Regulatory Affairs Manager please call Julie Cooper on 07951 082482 to discuss this role. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Specialist - Devices - Worcestershire
Hereford and Worcester
Jun 8
Mary Bolt is recruiting for a Senior Regulatory Affairs Specialist to join a company in the Medical Device industry who manufacture and deliver products across...
Regulatory Affairs Specialist - Zuchwil, Switzerland
Zuchwil
Jun 8
Jocelyn Blackham is recruiting for a Regulatory Affairs Specialist to be based with a well known, global healthcare company with a varied portfolio of Medical...
Regulatory Affairs Manager- Hertfordshire, UK- Relocation Package
England
Jun 8
My client, a Regulatory Affairs Consultancy based in Hertfordshire, are seeking a Regulatory Affairs Manager to join them on a full time basis. This role is ideal for a Senior Regulatory Affairs Executive who is ready to take their next step into a Team Lead position.
Senior Regulatory Affairs Associate
, Kiev,Ukraine
Jun 8
As part of a multi-national project team, you will take the lead to coordinate the compilation, review and submission of regulatory agency applications for international clinical trials in compliance with international regulatory requirements as well as internal and client standard operating procedures (SOPs). Your knowledge of clinical trial regulations will enable you to support the sponsor for the development of optimized clinical trial submission strategies. ...
Junior Regulatory Affairs Associate (1 year contract)
, Kiev,Ukraine
Jun 8
As part of a multi-national project team, you will take the lead to coordinate the compilation, review and submission of regulatory agency applications for international clinical trials in compliance with international regulatory requirements as well as internal and client standard operating procedures (SOPs). Your knowledge of clinical trial regulations will enable you to support the sponsor for the development of optimized clinical trial submission strategies. ...
Global Regulatory Consultant
Buckinghamshire
Jun 7
Regulatory Professionals are currently working with a global leader within the life sciences sector with expertise in drug discovery and the development and use of new therapies.
Regulatory Affairs Manager
Runcorn
Jun 7
My client is a rapidly expanding Pharmaceutical organisation, who has a vacancy in their Regulatory team. They are actively looking to hire a Regulatory Affairs Manager to their team on a permanent basis in the North West of England.
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Senior Regulatory Writer - Home Based – UK - £60,000 + 36 days holiday + bonus + benefits
Home based, UK
Jun 5
We are a leading consulting company looking for a Medical Writer to join our close-knit team and support in a home-based capacity with one of our pharma clients. The ideal candidate would have worked with a broad range of clinical documents and are capable of taking on an independent position in the business.
Global Regulatory Project Manager
Buckinghamshire
Jun 5
Regulatory Professionals are collaborating with global pharmaceutical organisation to recruit a Global Regulatory Project Manager who will focus on new product licensing strategies.
Regulatory Affairs Manager
Buckinghamshire
Jun 5
We are currently assisting a Bio-pharmaceutical company who have an excellent opportunity available for a highly experienced Regulatory Affairs Manager.
Regulatory Affairs Officer
Surrey
Jun 5
Regulatory Professionals are collaborating with a well-known pharmaceutical organisation to recruit for Regulatory Affairs Office. This company has an impressive pipeline of up and coming drugs.
Regulatory CMC Manager
Switzerland
Jun 5
For our client, one of the world’s leading pharmaceutical companies, we are currently looking for a Regulatory CMC Manager
NEW CONTRACT ROLE Regulatory Publishing Manager UK
UK, M4 Corridor
Jun 5
We have a great role for a Regulatory Publisher to join a dynamic and expansive international Biopharmaceutical company that provides opportunities for individuals to excel in a collaborative, team-based environment. If you wish to apply for this role, please send your CV with a covering note to oli.dimitrov@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Oli in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Supervisor - Flexible location in Ireland
Dublin, Republic of Ireland
Jun 5
Our client, a global medical devices company, are currently recruiting for a Regulatory Affairs Supervisor for their RA EMEA division. This role can be home-based or based in their office in South Dublin or the Midlands. This is a 6 month contract.
Manager/Senior Manager of Regulatory Services
Hartley Wintney
Jun 5
TMC Pharma Services are seeking a full time, office based Regulatory Manager/Senior Manager.Primary duties will include being the regulatory lead on global clinical studies and submission/maintenance and tracking of CTAs. There are also potential opportunities to get involved with other regulatory consulting projects.
Global Regulatory Consultant
Buckinghamshire
Jun 5
Regulatory Professionals are assisting a global healthcare company based in Buckinghamshire who are seeking an experienced Global Regulatory Consultant.
Regulatory Affairs Project Manager – Use your Lifecycle exp. to gain better clinical development and CeP experience
Belgium
Jun 4
Working in a strong EU regulatory team, you will also be learning from experienced GRL’s (in the same office), who will help to coach and develop your experience until you are ready to make the leap up to a Global Regulatory Leader. To have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
regulatory jobs : 100 +
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