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Jobs: (Regulatory)

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OPTION SUISSE Regulatory Bio CMC Director Global role on mAbs Are you of a pioneering mind and want to stretch yourself
Switzerland
Jul 20
OPTION SUISSE ** Regulatory CMC Director *** Pure mAbs & Team Management role ** Development & Marketed, US and Europe & Int’l Majors? This role is based in Switzerland, within easy commute of Lausanne, Geneva, or Bern. The role comes with an advantageous package including RSUs.
Senior Regulatory CMC Associate - Specialty Pharma - UK, Home based
UK - Home based
Jul 20
Meet are currently partnering with a specialist Pharma who are looking for a Senior Regulatory CMC Associate to coordinate the preparation of CMC documentation to support regulatory submissions across global territories.
Director Project Management (Regulatory Affairs and Pharmacovigilance FSP)-148371
Europe, Middle East and Africa-United Kingdom, Europ
Jul 20
This is an opportunity for an experienced Project Manager to join our Functional Service Partnership (FSP) team focussing on PPD's expanding Global Regulatory Affairs and Pharmacovigilance portfolio.   The role will work effectively across multiple functional areas to direct the delivery of FSP projects within quality, time, and cost requirements. ...
Regulatory Affairs Manager
Netherlands
Jul 20
Regulatory Affairs Manager, NetherlandsAn exciting opportunity has arisen to join this well-known global company and manage their regulatory activities. You will be involved in the entire life-cycle of products as well as, team management. ...
Qualitätsmanagementbeauftragter/Regulatory Affairs (m/w)
Villingen-Schwenningen (78052)
Jul 19
Qualitätsmanagementbeauftragter/Regulatory Affairs (m/w)Office-based in Villingen - Schwenningen Mein Kunde ist ein Familienunternehmen in der Medizintechnik-Branche mit langer Tradition und großer Erfolgsgeschichte, die bis heute anhält. ...
Medical Device expert (Regulatory Affairs)
England
Jul 19
Medical Device expert (Regulatory Affairs)! Apply now by clicking on the link below:
Regulatory Consultant CMC
Macclesfield
Jul 19
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team. They are looking to recruit a Regulatory CMC Consultant on a 12 Month contract basis to their offices in the North West.The Role:My client has a position available for an individual who shares our passion to join the Regulatory Documentation team, Documentation for the CMC part of submissions is one of the key project deliverables from Pharmaceutical Development. ...
Chief of Quality and Regulatory
England
Jul 19
Chief of Quality and Regulatory Affairs Birmingham £ 100,000
Regulatory Information Manager
United Kingdom
Jul 19
5 month contract Regulatory Information Manager Location: UK     TalentSource Life Sciences is currently searching for an experienced Regulatory Information Manager to work with one of our partner pharmaceutical companies in the South of England.     This is a freelance position with TalentSource for 5 months with the possibility of being extended, on a full time basis.
Regulatory Affairs Specialist
Netherlands
Jul 19
Regulatory Affairs Specialist, NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. ...
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Regulatory Affairs Specialist
Netherlands
Jul 18
Regulatory Affairs Specialist, NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. ...
OPTION SUISSE Regulatory CMC Director Pure mAbs and Team Management role Development and Marketed, US and Europe and Int’l Majors
Switzerland
Jul 18
OPTION SUISSE ** Regulatory CMC Director *** Pure mAbs & Team Management role ** Development & Marketed, US and Europe & Int’l Majors? This role is based in Switzerland, within easy commute of Lausanne, Geneva, or Bern. The role comes with an advantageous package including RSUs.
Regulatory Affairs Project Manager – Use your Lifecycle exp. to gain better clinical development and CeP experience
Belgium, Brussels
Jul 18
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 Affairs Contract – 12months “Cover CTA’s, PiPs and Scientific Advice prep for EU development Projects”
UK, M4 Corridor
Jul 18
We have a 12 month contract role for an expanding client in the M4 Corridor where you will be preparing scientific and regulatory documents for submission, providing input into development plans and creating regulatory strategy proposals. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com and call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
QA Systems Officer Contract Have you supported CAPAs for PhV and Regulatory Systems 6 months ROLLING
Belgium, Brussels
Jul 18
We have a 16 week contract role for a Global Regulatory Compliance Officer with an expanding Pharmaceutical company based in Brussels, Belgium. If you wish to apply for this role, please send your CV with a covering note to oli.dimitrov@advregulatory.com or alternatively, call Oli in the London office on +44 (0)20 7801 3388.
Regulatory Affairs Manager (m/w)
Germany
Jul 18
Unser Kunde sucht nach einem Regulatory Affairs Manager (m/w) in München.Wenn Sie viel Erfahrung mit eCTDs und IMPDs mitbringen sowie als POC für EMA und FDA agiert haben, habe ich eine ideale Stelle in München für Sie.Büro in München mit einer Möglichkeit übers Wochenede schnel nach Italien, Schweiz oder Österreich Ausflüge zu machen. Tolles Produktportfolio, nette Arbeitsatmosphäre sowie attraktives Gehaltspaket runden diese Posiiton ab. ...
(Regulatory Affairs) CMC Emerging Market Liaison
Cambridge
Jul 18
Associate Director of CMC Regulatory / LAM Liaison
Senior Drug Regulatory Affairs Manager
Basel
Jul 18
Our client, a dynamic bio-pharmaceutical company, is looking for a Senior Drug Regulatory Affairs Manager for a permanent role based in the Basel area, Switzerland. The ideal candidate should have at least 3 years of experience as Regulatory Affairs Manager, being responsible for the Clinical Trial Applications (CTAs) to regulatory authorities worldwide including submission and maintenance.
Senior Regulatory Specialist - Clinical Trials
England
Jul 18
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 Submission Manager 12117-1
Kent
Jul 18
Our client a Global Pharmaceutical Company has opened a new vacancy and is looking to recruit a Regulatory Submissions Manager on an initial 12 Month contract to be based at their offices in Kent.
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OPTION SUISSE Regulatory CMC Leader Biologicals Live Work Ski in this great location working for an expanding biotech Relo Offered
Switzerland
Jul 18
The position comes with full support for moving and relocation, and a Director level salary and bonus, as well as the normal Swiss benefits. This role is open to any European or US candidate, who has worked on EU or US submissions for regulatory CMC biologicals as a CMC RA Bio Lead, has submitted at least 1 major MAA or a set of major variations, and now wants to move to a global role
Regulatory Affairs Manager CMC Hamburg (m/w)
Germany
Jul 18
Für unseren Kunden aus Hamburg sind wir auf der Suche nach einen Regulatory Affairs Manager CMC. Ein schnellwachsendes Unternehmen mit einer arbeitnehmerorientierten Unternehmensstruktur und 38 Stunden Arbeitswoche.Das interne Fortbildungsprogramm unterstützt Sie bei Ihrer zukünftiger Karriere. ...
Regulatory Affairs Manager/Lead (HPRA and European Submissions)
Dublin
Jul 18
Responsibilities: * Management of all regulatory and development projects relevant to UK brands * Manage/ oversee regulatory strategies and the preparation of regulatory documents targeted at the Irish/European Markets. * Monitoring, collecting, interpreting and applying all relevant legislation, regulatory issues & trends and regulatory guidelines in the UK and keep the UK business up to date on national regulatory trends, risks and opportunities. ...
Regulatory Affairs Manager CMC (m/w)
Germany
Jul 18
Aufgaben: * Betreuung der operativen Aufgaben für den Bereich Regulatory Affairs CMC im Rahmen der Zusammenarbeit mit anderen Abteilungen, Ihren Regulatory Affairs Kollegen, sowie externe Partner und Hersteller. * Die Erstellung diverser CMC/Qualitätsrelevante Dokumente, wie z.B. die Qualitätsteile des IMPD, IND und des CTD (Modul 2.3 und 3). Dazu auch in Zusammenarbeit mit Ihren Kollegen in Regulatory Affairs auch Dokumente wie IBs, Briefing Books, DSURs usw. ...
Senior Regulatory Writer - Home Based – UK - £65,000 + bonus + benefits
England
Jul 17
We are a leading Medical Writing consulting looking for a Senior Medical Writer to join our close-knit team and support in producing a wide range of documentation for our clients. We pride ourselves in our welcoming culture and dedication to developing all members of our team to expand their skillsets.
Regulatory Affairs Associate
France
Jul 17
A rare opportunity as a Regulatory Affairs Associate 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. I can be reached on 0207255 6612 or ilyas.nur@secrecruitment.comIn your role as Regulatory Affairs Associate, you will be joining a team specialising in Cancer research. The company in question will enable you to work with professionals dedicated to improving the lives of millions.
Senior Regulatory Consultant
High Wycombe
Jul 17
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and are looking to recruit a Senior Regulatory Consultant on an initial 11 Month contract basis to be based at there offices in Buckinghamshire.The role will be involved with day to day Regulatory Activities related to providing strategic input within Development, Post Approval and Life Cycle Management. ...
Senior Regulatory Affairs Associate
London
Jul 17
Regulatory Professionals are currently collaborating with a top Global Bio pharma company with a truly exciting pipeline.
Regulatory Affairs Consultant – Cambridgeshire – 6 months +
England
Jul 17
Associated keywords: Medical device, Medical Device, Risk Management, ISO 14971, IEC 80002, IEC 62304, FDA Submission
Regulatory Affairs Officer / North West / North Wales
Chester
Jul 17
Regulatory Affairs Officer; Generics; North West/North Wales; MRP/DCP, Variations and Labelling; 1-2 years experience
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Senior Regulatory Executive - Ware, Hertfordshire
Ware
Jul 17
Jenni Woolley is recruiting for a Senior Regulatory Executive to join a science led global pharmaceutical company at their site based in Ware, Hertfordshire on...
CMC Regulatory Affairs Manager (m/w)
Germany
Jul 17
Für unseren Kunden aus Norddeutschland sind wir auf der Suche nach einen Regulatory Affairs CMC Manager.Ein schnellwachsendes Unternehmen mit ausgezeichneten Aufstiegsmöglichkeiten und erfolgreichem Work-Life-Balance Programm. Nicht nur die wissenschaftliche Affinität sondern auch eine Team-Orientierte Persönlichkeit ist für das Unternehmen sehr wichtig. ...
Regulatory Affairs Assistant
Nottingham
Jul 17
Job Role and Responsibilities: * To support product registration activities and product registration submissions throughout the world, in order that registrations are achieved in a timely manner in accordance with regulatory and Company requirements * Provide full support to all registration activities and regulatory submissions throughout the world. * Facilitate worldwide product registration activities by compiling appropriate dossiers, submissions and responses to regulatory bodies. ...
Regulatory Affairs Manager
Netherlands
Jul 17
Regulatory Affairs Manager , NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. Job Title: Regulatory Affairs Manager Location: Netherlands Benefits: Above market rate salary + fantastic benefits package Permanent position Job Responsibilities: * Determine appropriate regulatory strategy for proposed new products and initiate necessary activities. ...
Regulatory Writer – Small Pharma - Home Based – UK - £70,000 + bonus
Wales
Jul 16
We are a speciality pharmaceutical company looking for a Senior Medical Writer to join our team as our first Medical Writer and partner closely with clinical. The ideal candidate would have worked with a broad range of clinical documents and have submissions experience. This role is home based in the UK with occasional travel to the office. NOT ONCOLOGY.
Principle Regulatory Writer - Home Based – UK - £70,000 + car + bonus
Scotland
Jul 16
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.
Senior Regulatory Writer - Home Based – UK - £60,000 basic
Scotland
Jul 16
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.
Senior Regulatory Writer - Home Based – UK - £60,000 + 36 days holiday + bonus + benefits
England
Jul 16
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.
Regulatory Affairs – Project Manager/Consultant – Permanent - Home Based UK
Home based, UK
Jul 16
We are a leading global consultancy who are looking for an experienced regulatory professional with broad experience across regulatory affairs with a strong background in clinical trials and pre-approval to join our growing clinical team and support our broad range of pharma clients. The ideal candidates should have 4 years + in regulatory with experience in a client facing role. Consultancy and Project Management experience is a major bonus.
Regulatory Affairs Manager - Exciting Global Biopharma, Sussex/South England – upto £70,000 + Bonus + Benefits
West Sussex
Jul 16
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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Senior Regulatory Affairs Associate – Global Markets – London
UK, Central London
Jul 16
Amazing opportunity for an ambitious Regulatory person to join one of the world's leading OTC Consumer Healthcare businesses within their global team taking responsibility for the Regulatory management of a varied product portfolio.
Senior CMC Regulatory Affairs Associate – Global Markets – London
UK, London
Jul 16
My client is looking for an experienced regulatory affairs professional to join their established Regulatory team as a Senior CMC Regulatory Affairs Associate in London. This role is perfect for ambitious people who want to grow their career with a highly reputable company.
Senior Regulatory Affairs Project Manager
Maidenhead
Jul 16
Job Role: * Maintain marketing authorisations in Europe through the Centralised, Mutual Recognition and Decentralised Procedures, including preparation and submission of documentation to regulatory agencies. * Provide EU input to Global regulatory strategies to support LCM activities. ...
Regulatory Affairs Specialist
Singapore
Jul 16
ProClinical is seeking a Regulatory Affairs Specialist to be based in Singapore on a permanent basis. ...
Regulatory Affairs Specialist
Slough
Jul 16
We are working with a global specialty pharmaceutical company that is seeking a Regulatory Affairs Specialist to be based in Slough on a contract basis. Reporting into the UK and Ireland Head of Regulatory Affairs, the job holder will provide subject matter expertise into the planning and execution of regulatory and product complaint activities for the company’s UK and Ireland Operations. ...
Regulatory Affairs Manager
Scotland
Jul 16
Regulatory Professionals are currently collaborating with an internationally recognized pharmaceutical company who are seeking a Regulator Affairs Manager.
Senior Regulatory Submissions (Start-Up) Coordinator - UK
England
Jul 16
Medpace is looking for a Senior Regulatory Submissions (Study Start-Up) Coordinator to join our team in London or Stirling.
Regulatory Submission Coordinator - Germany
Germany
Jul 16
Our client is global CRO company who are seeking for all levels of experienced Regulatory Submission Coordinator in line with their continued growth to support their robust pipeline. The organisation is specialising in a multitude of therapeutic areas, and are active in over 45 countries across the globe.
Regulatory Affairs Manager LCM (m/w)
Germany
Jul 16
Für unseren Kunden aus Norddeutschland sind wir auf der Suche nach einen Regulatory Affairs LCM Manager.Ein schnellwachsendes Unternehmen mit ausgezeichneten Aufstiegsmöglichkeiten und erfolgreichem Work-Life-Balance Programm. Neue Büros mit einer besonders ausgeprägten Teamatmosphäre - wenn Sie keinen Spaß verstehen, wäre die Stelle wahrscheinlich nicht das richtige für Sie. ...
Regulatory Artwork Coordinator
Surrey
Jul 16
Our client a Global Pharmaceutical Company has opened a new vacancy and is looking to recruit a Regulatory Affairs Artwork Coordinator on an initial 12 Month contract to be based at their offices in Surrey.
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Regulatory Affairs Manager
Netherlands
Jul 16
Regulatory Affairs Manager , NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. Job Title: Regulatory Affairs Manager Location: Netherlands Benefits: Above market rate salary + fantastic benefits package Permanent position Job Responsibilities: * Determine appropriate regulatory strategy for proposed new products and initiate necessary activities. ...
Director, Regulatory Affairs
Singapore
Jul 14
Our client is looking for an experienced Director, Regulatory Affairs to supervise their industry activities in Asian. If you posses experience in the pharmaceutical industry with knowledge in OTC, we like to speak with you.
Regulatory Affairs Specialist - UK/France/Switzerland based
England/France/Switzerland
Jul 13
Regulatory Affairs Specialist - UK/France/Switzerland based
Regulatory Affairs Assistant
Wokingham
Jul 13
If you’re an existing Regulatory Affairs professional looking for a challenging new opportunity, it would be great to talk to you about a new role I’m handling.I’m working with a well-established Pharmaceutical company looking to recruit a Regulatory Affairs Assistant. ...
Regulatory Affairs Assistant
North Yorkshire
Jul 13
If you’re an existing Regulatory Affairs professional looking for a challenging new opportunity, it would be great to talk to you about a fantastic new role I’m handling. I’m working with a well-established specialist Pharmaceutical company looking to recruit a Regulatory Affairs Assistant. You will be responsible for product registrations activities as well as submissions globally.Knowledge of worldwide regulatory procedures for Medical devices is also desired. ...
Regulatory Affairs Specialist
Aberdeen
Jul 13
If you’re an existing Regulatory Affairs professional looking for a challenging new opportunity, it would be great to talk to you about a new role I’m handling.I’m working with a leading UK Pharmaceutical company looking to recruit a Regulatory Affairs Specialist.You will be responsible for providing Regulatory leadership for global regulatory affairs.As well as having a body of Regulatory Affairs experience you will also have experience with Medical devices. ...
OPTION SUISSE Regulatory Director CMC Biologicals FR speaking region Relocation offered Have strong EU MAA CMC Gain Global BLA experience
Switzerland
Jul 13
The position comes with full support for moving and relocation, and a Director level salary and bonus, as well as the normal Swiss benefits. This role is open to any European or US candidate, who has worked on EU or US submissions for regulatory CMC biologicals as a CMC RA Bio Lead, has submitted at least 1 major MAA or a set of major variations, and now wants to move to a global role.
OPTION SUISSE Regulatory CMC Associate Director Want to gain more region, be promoted and developed and work in a quickly expanding biotech
Switzerland
Jul 13
The position comes with full support for moving and relocation, and a Director level salary and bonus, as well as the normal Swiss benefits. This role is open to any European or US candidate, who has worked on EU or US submissions for regulatory CMC biologicals as a CMC RA Bio Lead, has submitted at least 1 major MAA or a set of major variations, and now wants to move to a global role.
Senior Manager, Regulatory affairs
Hatfield
Jul 13
Regulatory professionals are currently collaborating with a top Global Pharmaceutical company which has one of the best Oncological and neurological pipelines on the market.
Senior Regulatory affairs associate
West London
Jul 13
Regulatory Professionals are currently collaborating with a top Global Bio pharma company with a truly exciting pipeline, their key focus is to target life threatening diseases.
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Senior Regulatory Affairs Consultant - High Wycombe
High Wycombe
Jul 13
Jenni Woolley at CK Group is recruiting for a Senior Regulatory Affairs Consultant to join a company in the Pharmaceutical industry at their site based...
Regulatory Affairs Manager
Netherlands
Jul 13
Regulatory Affairs Manager , NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. Job Title: Regulatory Affairs Manager Location: Netherlands Benefits: Above market rate salary + fantastic benefits package Permanent position Job Responsibilities: * Determine appropriate regulatory strategy for proposed new products and initiate necessary activities. ...
Senior Regulatory Affairs Manager - remote
United States Anywhere, US None
Jul 13
Senior Regulatory Affairs Manager - Anywhere, US Office-based or Remote-based   Who We Are Synteract is a global full-service contract research organization with a successful three-decade track record supporting biotechnology, medical device and pharmaceutical companies. With our mission of ”Bringing Clinical Trials to Life,” we provide customized Phase I through IV services internationally, offering expertise across multiple therapeutic areas including notable depth in Oncology,...
International Regulatory Strategist
Welwyn
Jul 13
This position is responsible for leading the development and implementation of the International regulatory strategy for assigned products in Asia Pacific, Eastern Europe Middle East & Africa and Latin America. The International Regulatory Strategist is the relevant representative to global teams and affiliates for assigned products, ensuring the requirements of International countries are considered in development and registration plans. ...
Regulatory Affairs Specialist/Senior/Princial Regulatory Affairs Specialist - EMEA-148606
Europe, Middle East and Africa-UK-England-Cambridge,
Jul 13
PPD currently has opportunities for Regulatory Affairs Specialist/Senior/Principal Specialist.   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. ...
Freelance Regulatory Affairs Specialist - Dublin
Rep. Ireland
Jul 12
Support  regulatory activities for for a range of products. Submission of variation applications across all aspects of registered particulars. Managing deletions and divestitures as required, product acquisitions, quality issues and MA renewals. 
Regulatory Affairs Associate
Essex
Jul 12
A growing Speciality Pharmaceutical company based close to the Essex/ Cambridge border is actively looking for a Regulatory Affairs Associate to join their developing team.
Regulatory Affairs Associate
Essex
Jul 12
This emerging trans-Atlantic pharmaceutical group addressing the clinical needs of patients under specialist care, with an existing focus on gastrointestinal (GI) disease.
Regulatory Affairs Senior Associate
Maidenhead
Jul 12
ProClinical is working with a medium sized east coast US biopharma specializing in rare diseases. They are looking to appoint a Regulatory Senior Associate to work with the head of Regulatory Affairs to maintain the company's marketed product for a rare disease.This is an excellent opportunity for a regulatory professional to gain first hand practical experience of working with a high value drug which improves patients’ lives dramatically. ...
Regulatory Affairs Manager, Contractor
Ukraine Kiev, UA
Jul 12
Regulatory Affairs Manager, Contractor - Ukraine Ukraine   Who We Are Synteract is a global full-service contract research organization with a successful three-decade track record supporting biotechnology, medical device and pharmaceutical companies. With our mission of ”Bringing Clinical Trials to Life,” we provide customized Phase I through IV services internationally, offering expertise across multiple therapeutic areas including notable depth in Oncology, Neuro Degenerative...
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Regulatory Affairs Senior Lead
Netherlands
Jul 12
Regulatory Affairs Senior Lead, NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. ...
Regulatory Affairs and Quality Lead
Netherlands
Jul 11
Regulatory Affairs and Quality Assurance Lead, NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. ...
Senior Regulatory Affairs Associate - Global Pharma - Contract - UK
England
Jul 11
We are working with one ofthe largest Biotech in the world and are looking to expand their regulatory affairs team by bringing on a Senior Regulatory Affairs Associate. They are looking for someone to hit the ground running on a 12-month contract based in their Cambridge office.
Regulatory Affairs Lead
Netherlands
Jul 11
Regulatory Affairs and Quality Assurance Lead, NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. ...
Senior Associate Regulatory Affairs - 12 month contract
Uxbridge
Jul 11
Please apply via Pharmaweb or email tagray@planet-pharma.co.uk
Regulatory Officer Submissions
Dublin, Republic of Ireland
Jul 11
Our client, a global pharmaceutical company, are currently recruiting for a Regulatory Officer Submissions. This is a 12 month contract role initially.
Regulatory Affairs Specialist
Inverness - Scotland
Jul 11
12 month contract - Inverness - immediate start
Regulatory Affairs Specialist
England
Jul 11
Our Client, a global leader in serving science whose products address a range of needs from material characterisation and chemical analysist to clinical diagnoses is seeking a regulatory affairs specialist to join their team in England. ...
Regulatory Affairs Associate (London)
Hammersmith, United Kingdom
Jul 11
For our London, Hammersmith office we are currently looking for a Regulatory Affairs Associate. The primary responsibility of this role is the creation of regulatory packages and the development of regulatory strategy to achieve regulatory approvals and clearances worldwide expediently and consistently within all studies, interventional and non-interventional.
Senior Specialist, Global Regulatory Affairs (UK or Eastern EU~Home based)
Flexible Location
Jul 10
The Senior Specialist, Global Regulatory Affairs provides project representation and input to projects awarded to WCT for all stages of the drug development cycle.
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Regulatory Packaging and Artwork Manager
Edinburgh
Jul 10
Regulatory Professionals are currently collaborating with an expanding Bio pharmaceutical organisation who are looking to recruit for an interim Regulatory Packaging and Artwork Manager
Regulatory Affairs Manager - Some remote working and flexible hours.Great variety of work and work for a company that is different.
Oxfordshire
Jul 10
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
Jul 10
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 Officer - work on MAAs , post approval and all aspects of regulatory work
Oxfordshire
Jul 10
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Global CMC Regulatory Affairs Manager - Midlands
Midlands
Jul 10
To apply for this CMC Regulatory Affairs Manager please call Julie Cooper on 07951 082482 to discuss this role. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Associate
Cambridgeshire
Jul 10
This global pharmaceutical company is looking for a Regulatory Associate for their international regulatory affairs team in Cambridgeshire.
Regulatory Affairs Senior Director
Belgium
Jul 10
Regulatory Affairs Senior Director, BelgiumAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of products. ...
Regulatory Affairs Manager - Pharma, UK
Scotland
Jul 9
Regulatory activities associated with worldwide development including development of regulatory strategy, due diligence, gaining regulatory approvals for clinical trial and marketing applications and maintenance of these authorisations where appropriate.
Regulatory Associate- 73822
Worthing
Jul 9
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and are looking to recruit a Regulatory Consultant - on an initial 12 Month contract basis to be based at their offices in West Sussex
Regulatory Affairs Senior Officer - 12036-1
Berkshire
Jul 9
My Client a Global Pharmaceutical Company has opened a new vacancy and is looking to recruit a Regulatory Affairs Senior Officer on an initial 6 Month contract to be based at their offices in Berkshire.
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Regulatory Affairs Senior Officer
Berkshire
Jul 9
My Client a Global Pharmaceutical Company has opened a new vacancy and is looking to recruit a Regulatory Affairs Senior Officer on an initial 6 Month contract to be based at their offices in Surrey.
Team Leader Regulatory Affairs (m/w) Frankfurt
Germany
Jul 9
Für unseren Kunden aus Frankfurt suchen wir nach einem erfahrenen Teamleiter für die Regulatory Affairs Department.Das Unternehmen gehört zu den attraktivsten Pharmaunternehmen der DACH Region. Klare Karrieremöglichkeiten sowie ein attraktives Gehaltspaket zeichnen unseren Kunden aus. ...
Regulatory and Start-Up Specialist 2 (f/m) - office-based in Espoo, Finland
Espoo
Jul 9
PURPOSEManage and perform tasks at country level associated with Regulatory, Start-Up (RSU) and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May participate in pre-award activities, proposals and oversights of the scope of work at country level. ...
QA Regulatory and QMS Manager - Worthing
Worthing
Jul 9
Jennifer Woolley is recruiting for a QA Regulatory and QMS Manager to join a company in the Pharmaceutical industry at their site based in Worthing...
Senior Associate Regulatory Affairs Labelling - Oxford - contract
Oxford
Jul 9
Planet Pharma was founded by a dedicated team of seasoned professionals with extensive experience supporting the pharmaceutical, biotechnology and device industries. Our goal was to create an organization that strengthens the employer-employee dynamic by connecting clients with talent — ultimately making staffing more personal and creating enduring, valuable relationships.
Regulatory Affairs Associate Director
Belgium
Jul 9
Regulatory Affairs Associate Director, BelgiumAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of products. ...
Regulatory Specialist
Spain
Jul 7
We are currently looking for a Regulatory Specialist to join a global CRO, home based role in several Emea Countries
Regulatory Specialist
Spain
Jul 7
This is a great opportunity for someone with a good grounding in these subjects and tasks
Regulatory Affairs Associate Director
Belgium
Jul 6
Regulatory Affairs Associate Director, BelgiumAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of products. ...
Regulatory Executive - Ware
Ware
Jul 6
Jennifer Whoolley is recruiting for a Regulatory Executive to join a company in the Pharmaceutical industry at their site based in Hertfordshire on a 12...
regulatory jobs : 100 +
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The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.