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The latest Regulatory jobs - BETA

Jobs: (Regulatory)

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Regulatory Affairs Specialist
Stuttgart
Mar 28
Regulatory Affairs Manager (m/w)Office-based in Stuttgart vollzeit/ unbefristetAufgaben: * Stetige Beachtung und Überarbeitung der regulatorischen Anforderungen in der Zulassung * Erstellung der technischen Dokumentation für die Zulassung * 510(k) Dossier- Erstellung * Durchführung von Design Reviews * Teilnahme und Durchführung interner und externer Audits * Ansprechpartner für Fragen hinsichtlich der regulatorischen Anforderungen für Medizintechnik-Produkte * Schnittstelle interner ...
PW-6859 EU Regulatory Project Manager
England
Mar 28
Opportunity for a Regulatory Project Manager to join a Global Pharma and oversee a EU remit including both a development and marketed portfolio. Office based to the West of London.
Junior Regulatory Affairs Manager - you need 3-4 years experience in regulatory - do you have CMC or Clinical experience Midlands based
Nottingham
Mar 28
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 - Beautiful and historic Ghent- Belgium- Medical Devices expert - Global role
Belgium
Mar 28
To apply for this Regulatory Affairs role please call Julie Cooper on 07951 082482 or please send your CV to:julie@mosaicrecruitment.co.uk
Associate Director - Regulatory Affairs - Refreshing ways of work- Great regulatory work , can work remotely and flexibly when you want
Oxfordshire
Mar 28
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 SOLUTIONS ANALYST-UNITED KINGDOM
London,United Kingdom
Mar 28
PRA Health Sciences is excited to offer new opportunities within our new partnership agreement with a global pharmaceutical company. We have openings for Regulatory Solutions Analyst join us supporting our Global embedded team with one of the industries largest international companies based out of their London HQ. This is a permanent opportunity, office based in Central London.
Senior Regulatory Affairs Manager- Varied regulatory projects in a visionary company remote working and flexible hours - Oxfordshire
Oxfordshire
Mar 28
To apply for this Regulatory Affairs Manager please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Associate Director - Regulatory Affairs - Can work remotely and flexible working hours. Great regulatory work in a company with great work ethic
Oxfordshire
Mar 28
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 Manager - Some remote working and flexible hours.Interesting regulatory projects. Visionary company
Oxfordshire
Mar 28
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Labelling Director - Recognized as expert in global labeling, EU/US labeling, and (CCDS)- London- can work remotely 2 days
London
Mar 28
To apply for this Regulatory Affairs Labelling Director please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
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Global Regulatory Labelling Director - US and EU experience - Lead a team - 3 days in office and 2 remotely - Central London
London
Mar 28
To apply for this Regulatory Affairs Labelling Director please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Senior Officer
England
Mar 28
Regulatory Affairs Senior Officer Hertfordshire Would you like the opportunity to work for a leading Pharmaceutical company? Do you want to work within an international and ambitious team?
Country Head of Regulatory Affairs UK – Consumer Healthcare
South East England
Mar 28
I am currently partnering with a leading global in the Consumer Healthcare space. They are appointing an experience Regulatory Affairs head to manage a large UK based team, leading on the design and implementation of regulatory strategy for new products across numerous therapeutic categories.
Global Regulatory CMC expert
Geneva
Mar 28
Hydrogen partners Global Biopharmaceutical companies for the scouting of Regulatory Affairs experts with complex skillsets. A great opportunity for a CMC expert with experience in global Regulatory Affairs has arisen with a renown Biopharmaceutical company based in Geneva. They are further developing technologies across Oncology, Gastroenterology, Renal and Urinary. ...
Junior Regulatory Affairs - constant career progression / international company
Sofiacity district
Mar 28
A fantastic Junior Regulatory Affairs Job opportunity for an excellent communicative Graduate Regulatory Manager to join an international growing pharmaceutical company. This position offers the...
Senior / Specialist Regulatory Affairs - constant career progression / international company
Sofiacity district
Mar 28
A fantastic Regulatory Affairs Manager Job opportunity for an excellent communicative Regulatory CMC Manager to join an international growing pharmaceutical company. This position offers the...
Senior CMC Regulatory Affairs Expert
Basel
Mar 28
Hydrogen partners with Swiss Pharmaceutical companies to bring them the most competent experts in CMC Regulatory affairs. A great opportunity has just arisen for a CMC expert to join the Regulatory Affairs team of a Drug Pharma company based in Basel, focused on the development of products for respiratory diseases. They currently have 3 specific respiratory products in Ph. II and they are also expanding their clinical development activities to study of a new class of innovative drugs. ...
SSU and Regulatory Specialist II (Czech Republic)
Czech Republic
Mar 28
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
Senior Regulatory Intelligence Manager - Surrey- up to £65k
Surrey
Mar 27
Are you an ambitious regulatory affairs manager with expertise in legislation for technical and regulatory aspects of ethical unlicensed medicines? I am looking for an experience manager to join the team to manage and maintain global relationships and devise regulatory strategies across the full drug life cycle.
Regulatory Intelligence Consultant
Surrey
Mar 27
An internationally known pharmaceutical company situated in the UK and operating in over 150 markets worldwide is looking to hire a Regulatory Intelligence Consultant. The company develops a broad range of products in pharmaceuticals, vaccines and consumer healthcare. ...
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Home Based – Regulatory Writer – Global CRO – 12 Month Contract
England
Mar 27
This world leading CRO is after experienced medical writers who can come in on a contract basis and hit the ground running. This position is 100% home based allowing you to work on a range of global projects.
Home Based – Regulatory Writer – Global CRO – 12 Month Contract
England
Mar 27
This world leading CRO is after experienced medical writers who can come in on a contract basis and hit the ground running. This position is 100% home based allowing you to work on a range of global projects.
Regulatory Affairs Associate- Medical Devices
Scotland
Mar 27
Regulatory Associate/Senior- Medical Devices- Scotland
Regulatory Submissions Manager
Munich
Mar 27
Unsere Kundin, eine globale CRO, sucht eine/n erfahrenen Regulatory Submissions Manager für ihr Clinical Operations Team. Die Position ist office-based im schönen München. Die Stelle ist auch für Senior CRAs geeignet, die nicht mehr reisen möchten.. ...
Regulatory Intelligence Consultant
Surrey
Mar 27
ProClinical is currently recruiting for a regulatory affairs job on behalf of a top 10 global pharmaceutical company located in Surrey, UK. Our client has a vacancy for a Regulatory Intelligence Consultant on a contract basis. ...
Regulatory Consultant - UK/Ireland
Middlesex
Mar 27
An attractive job opportunity has arisen at a leading multinational pharmaceutical company. They are seeking a Regulatory Consultant to work at their UK site in Middlesex. The company employs 100,000 personnel across 150 countries, working across multiple therapy areas including cardiovascular, oncology, and respiratory.Job Role:Responsible for the regulatory management of marketing authorisations (MAs) for a therapy area and is the primary interface with the regulatory authorities. ...
Regulatory Consultant- Development
Middlesex
Mar 27
Regulatory Development Consultant- Big Pharma- Middlesex
Regulatory Intelligence Consultant
Surrey
Mar 27
Regulatory Intelligence Consultant- 6 Months- Big Pharma- Surrey
Regulatory Affairs Specialist
Frankfurt
Mar 27
Unser Kunde, ein globales Medizinprodukteunternehmen, sucht eine/n Regulatory Affairs Manager office-based in Frankfurt am Main. ...
Regulatory Affairs Consultant - CMC
Kent
Mar 27
Regulatory Affairs Consultant- CMC- South East England- 6 Months Contract
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Regulatory Program Manager
Basel
Mar 27
I have a great opportunity of "Regulatory Program Manager" for a contract position of 10 months in Switzerland. ...
Regulatory Affairs Manager and Client Engangement
Ingelheim am Rhein (55218)
Mar 27
Our client is a market leading management consultancy. Their Life Sciences Vertical focuses on providing services to support customers to run their existing business better and to develop their business model further to succeed in the drug development and clinical trials phases.To support a client site in Germany, they need experience in Clinical Regulatory Affairs while having impecible communication skills. ...
(URGENT) / Contract or Perm - Regulatory Affairs Specialist required for expanding Med Dev Company…
Hertfordshire
Mar 27
(URGENT) / Contract or Perm - Regulatory Affairs Specialist required for expanding Med Dev Company…
Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
Mar 24
Tec Group international has partnered with a global Pharmaceutical company to find a regulatory profile to help lead the business and Regulatory departments. This position offers a creative platform for the chosen candidate to work on projects and areas they excel in. This position is based in Boston and offer a competitive salary and package. For more info please contact Sam Murphy at TEC Group sam.murphy@tecgroup.net
Regulatory Associate II
Cambridge
Mar 24
Senior Regulatory Affairs Associate CMC - CambridgeJOB SUMMARY:i-Pharm Regulatory have a Senior Regulatory Affairs Associate position which will focus on supporting Global CMC which may include Emerging Markets. Excellent opportunity to grow your Regulatory experience across a wide range of territories with a Top 5 Biotech.Candidates must be eligible to work in the UK. ...
Regulatory Affairs Consultant
Switzerland
Mar 24
Edelway SA is a Swiss professional services company. From our offices in Switzerland, Spain and Germany we provide personnel to our multinational clients in Switzerland and worldwide. We are now looking for a Regulatory Affairs Consultant to join our multinational Life Sciences client in the St. Gallen area, Switzerland.
URGENT: Regulatory Labelling Consultant - East Kent, UK
England
Mar 24
Just Pharma are seeking a regulatory professional with experience in labelling to join a pharmaceutical company in East Kent.
Regulatory Affairs Manager (m/w)
Hamburg
Mar 24
Regulatory Affairs Manager (m/w)Office-based in Hamburg – vollzeit/ unbefristetAufgaben:- Erstellung und Prüfung von Zulassungsdokumenten- Sicherstellung der Einhaltung regulatorischer internationaler Anforderungen- Planung von Strategien zur Qualitätssicherung- Durchführung von Konformitätsbewertungen- Entwicklung, Gestaltung und Optimierung von Qualitätsmanagementsystemen- Ausarbeitung von Strategien zur Optimierung der Entwicklungsprozesse- Schnittstelle der zu den angrenzenden Fachbereic ...
Manager Regulatory Affairs (m/f)
Villingen-Schwenningen (78052)
Mar 24
Manager Regulatory Affairs/ Schwerpunkt Disposables (m/w)Office-based in Villingen- SchwenningenAufgaben:- Erstellung technischer Dokumente für die Zulassung von Medizinprodukten- Stetige Prüfung der regulatorischen Anforderungen während des Zulassungsprozesses- Schnittstelle für alle zugehörigen angrenzenden Fachbereiche- Prüfung und Anpassung der Prozesse vor dem Hintergrund der ISO 13485- Schlüsselperson in der Kommunikation mit den internationalen Teams- Begleitung von internen und exte ...
Regulatory Officer
Hampshire
Mar 24
An exciting Regulatory Affairs Associate job opportunity for a proactive life science graduate to work in a growing British pharmaceutical company based in South Hampshire....
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Senior Regulatory Affairs Associate
Sydney
Mar 24
A Senior Regulatory Affairs Associate is required for a mid-sized pharmaceutical company. They have both Rx and generic product lines.
Regulatory Associate - Melbourne
South Eastern Suburbs Melbourne
Mar 24
A Regulatory Affairs Associate is required for a mid sized global pharmaceutical company with a unique pipeline and solution offering.
Regulatory Compliance Manager
Singapore
Mar 23
Reporting directly to the Regional Head for Healthcare Business in APAC, providing leadership to both quality and regulatory teams,and supporting business development within a leading third party distribution company.
Regulatory Affairs Manager
Singapore
Mar 23
As part of the Quality and Compliance Group, provide Regulatory Affairs expertise in new product development, technical file creation and global registrations.
Regulatory Affairs Manager (m/w) Freiberufler
Germany
Mar 23
Regulatory Affairs Manager (m/w) Freiberufler/Freelancer
Regulatory Submissions Coordinator
Lyon
Mar 23
POSITION SUMMARY Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our team. ...
Study Start up - Regulatory Submissions Coordinator
Prague
Mar 23
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. ...
Senior regulatory consultant
London
Mar 23
A global biotechnology company is recruiting for a Senior Regulatory Consultant, to join their team in London, UK. This role will be on a 6 month contract with the potential for some home-based working. This will be a very EU-focused role. ...
Regulatory Affairs Manager (m/w) in der Medizintechnik
Bremen
Mar 23
Regulatory Affairs Manager (m/w)Office-based in Bremen - vollzeit, unbefristetAufgaben:- Durchführung technischer Dokumentationen für Medizinprodukte- Begleitung von Entwicklungsprojekten von Klasse III Produkten- Durchführung von Usability Tests gemäß IEC 62366 - Identifizieren der Weltweiten regulatorischen Anforderungen an Geräte und Software- Entwicklung von Prüf-, und Zulassungsstrategien für den Vertrieb- Durchführung und Begleitung externer und interner Audits- Schnittstelle zu den a ...
Senior Regulatory Consultant
London
Mar 23
ProClinical is seeking a Senior Regulatory Consultant on behalf of a global biotechnology company, to join their team in London, UK. This role will be on a 6-month contract with the potential for some home-based working. This will be a very EU-focused role. ...
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Global Regulatory Labelling Director - US and EU experience - Lead a team - 3 days in office and 2 remotely - Central London
London
Mar 23
To apply for this Regulatory Affairs Labelling Director please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Officer
Maidenhead
Mar 23
My client is a new entrant into the UK market and seeking to recruit a Regulatory Affairs Officer to be based in newly refurbished offices attached to a state of the art manufacturing facility. This organisation is likely to be a major player in the generic drug field in the UK over the next few years.Job Overview:This position would suit an individual looking to further their experience in regulatory affairs, this is likely to be a popular position but 2 roles are available at this level. ...
PW-6850 Senior Regulatory Affairs Associate CMC
England
Mar 23
This role, for a global specialty pharmaceutical company will have responsibility for managing the CMC aspects of Regulatory Affairs and support other regulatory work for all medicinal products, including the development and implementation of optimal regulatory strategies and thereby ensuring regulatory and commercial success.
Senior Regulatory and Site Services Specialist - office based in Leuven
Belgium
Mar 23
We are looking to recruit a Senior Regulatory and Site Services Specialist - office based in Leuven
PW-6849 Regulatory Affairs Manager
England
Mar 23
This role, for a global specialty pharmaceutical company, will have responsibility for managing and developing the Regulatory Affairs Team and maintain the product portfolio. You will lead the development and implementation of optimal regulatory strategies to ensure regulatory and commercial success for the UK and Ireland as well as supporting European markets
OPTION BENELUX Regulatory ONCOLOGY Associate Director P2B / P3 NMEs, mAbs, ADCs, Nibs andgt;andgt; Sr RA Project Manager MULTIPLE filings
Nr Amsterdam
Mar 23
OPTION BENELUX *** Regulatory ONCOLOGY Associate Director *** P2B and P3 NMEs, mAbs, ADCs, Nibs >> Senior RA Project Manager MULTIPLE filing Opportunities
Regulatory Affairs Manager - San Fran
bay area
Mar 23
For more information or to apply for the position please contact Sam Murphy at the TEC Group International. 0208 544 3224 / sam.murphy@tecgroup.net
Director, Global Regulatory Affairs; Immuno-Oncology
Boston
Mar 23
Director, Global Regulatory Affairs; Immuno-OncologyTec Group international has partnered with a global Pharmaceutical company to find a regulatory profile to help lead the business and Regulatory departments. This position offers a creative platform for the chosen candidate to work on projects and areas they excel in. This position is based in Boston and offer a competitive salary and package.
Regulatory Affairs / Regulatory / RA / Project Management / Manager / ISO 13485 / Medical Devices /
Wiltshire
Mar 23
Job Title: Regulatory Affairs Project ManagerLocation: WiltshireSalary: £50,000 - £65,000This position is responsible for managing all facets of regulatory support to market products, developing regulatory submissions, managing departmental projects.  In addition, the position will supervise the development and creation of labelling, provide guidance and consultation for domestic and international regulations and interact with governmental agencies. ...
Regulatory Affairs Assistant Part-Time - Herts
Hertfordshire
Mar 23
Oliver Care is recruiting for a Part-Time Regulatory Affairs Assistant to join a company in the Pharmaceutical CRO industry at their site based in Hertfordshire...
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Regulatory Manager (12 Month Contract)
Middlesex
Mar 23
i-Pharm Consulting are recruiting for…ROLERegulatory Affairs LOCATION: Middlesex Or Cambridge RATE: Negotiable ROLE: Leading Biotech are looking for a Regulatory Manager to focus on CTA and MAA applications.This includes the compilation of regulatory documents as well as providing strategic input for centralised submissions. PIP’s and Orphan drug designations will also be an area of focus. ...
Senior Regulatory Associate (CMC)
Middlesex
Mar 23
Senior Regulatory Affairs Associate, Global Pharma Senior Regulatory Affairs Associate required for a dynamic global pharmaceutical company based in West London. ...
Senior Regulatory Affairs Manager CMC- South England - £65,000-£80,000
Cambridge
Mar 23
As a senior manager within the regulatory CMC team you will be responsible for activities internationally providing strategy, CMC updates, advice to various teams including Regulatory strategy team leads, due diligence exercises, preparation of compliant regulatory documentation including CTAs, MAAs, all life cycle maintenance activities and providing scientific advice where necessary.
Junior Regulatory Affairs Manager - you need 3-4 years experience in regulatory - CTA or CMC experience needed
Nottingham
Mar 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 Operations Manager (m/w)
München
Mar 22
Regulatory Operations Manager (m/w)Office-based in MunichJob Description:- Consulting clients on a wide range of regulatory and technical problems through all stages of product development; Specifically regarding electronic Publishing – eCTD, Docubridge, Regulatory Information Management Systems and Regulatory Databases.- Train, mentor and lead project teams specifically in the product development stages building up to market authorization. ...
Senior Regulatory Affairs Manager (m/w) CMC
München
Mar 22
Senior Regulatory Affairs Manager (m/w) CMCOffice-based in MünchenAufgaben:- Planung, Koordination und Durchführung regulatorischer Aktivitäten für unsere Entwicklungsprogramme mit den involvierten Abteilungen (CMC Operations & Qualitätskontrolle, Präklinik, Klinik und Qualitätssicherung)- Teilnahme in Projektteams und Ansprechpartner gegenüber externen Partnern und Lohnherstellern in regulatorischen Fragestellungen- Erstellung, Zusammenstellung und Pflege von IMPDs, INDs, Briefing Books und ...
Director Regulatory Strategy and Intelligence – research driven company – West Germany – 140,000 €
Germany
Mar 22
We are looking for an experienced regulatory manager, who will help us drive business growth by providing his knowledge in regulatory intelligence and strategy. This is a new developed position and plays a key role within the whole organization.
Regulatory Affairs Manager Medizinprodukte / aufstrebendes Unternehmen
Mecklenburg Vorpommern
Mar 22
Eine einmalige Chance als Regulatory Affairs Manager im Bereich medizinische Geraete und Produktzulassung der Klasse 1 -3, Teil eines international aufstrebenden Unternehmens zu werden. Um...
Regulatory Affairs Manager
Baden Württemberg
Mar 22
Eine einmalige Chance als Studienabsolventen und Regulatory Affairs Specialist im Bereich medizinische Produkte der Klassifizierungen 1 bis 3, Teil eines global operierenden Unternehmen zu werden....
Part-time Regulatory Affairs specialist
Den Haag
Mar 22
As a Regulatory Affairs Specialist within a fast growing contract development and manufacturing organization you will be responsible for product submissions, license renewals, periodic updates and registrations to regulatory agencies.
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Regulatory Affairs Manager (m/w) in der Medizintechnik
Bayern
Mar 22
Regulatory Affairs Manager in der Medizintechnik (m/w)Office-based in Bayern unbefristet- VollzeitAufgaben:- Sie sind für die Erstellung und Überarbeitung der technischen Dokumentation zuständig- Sie bereiten interne Audits vor und führen diese durch- Sie durchleuchten die unternehmerischen Prozesse und leiten davon Strategien ab- Sie sind Leiter von Schulungen aller Thematiken hinsichtlich des Bereichs Regulatory Affairs- Außerdem sind Sie Ansprechpartner in allen regulatorischen Belangen f ...
Regulatory Affairs Manager - Some remote working and flexible hours.Great variety of work and work for a company that is different.
Oxfordshire
Mar 22
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Global Regulatory Labelling Director - US and EU experience - Lead a team - 3 days in office and 2 remotely - Central London
London
Mar 22
To apply for this Regulatory Affairs Labelling Director please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Specialist / RA / CE Marking / Technical Files / Submissions / Pre-market Approva
Cambridgeshire
Mar 22
Regulatory Affairs Specialist / Regulatory / RA / ISO 13485 / Medical Devices / Cambridgeshire / UKSalary: £40,000 - £50,000Location: CambridgeshireRegulatory Affairs Specialist / RA / ISO 13485 / Medical Devices specialist needed to join a growing medical device manufacturer in CambridgeshireRegulatory Affairs Specialist / RA / ISO 13485 / Medical Devices – Key responsibilities: CE Marking Submission applicationsSupport and provide guidance for EMEA registrationPrepare all future 510(k) su ...
Head of Regulatory Affairs, APAC
Singapore
Mar 21
I'm currently recruiting for a Head of Regulatory Affairs, to join our client's regional office in APAC. This role will support the global regulatory team and the regional regulatory representatives through providing regulatory leadership of a portfolio of products.
Quality and Regulatory Officer
Wales
Mar 21
Quality and Regulatory Officer An opportunity has just arisen for a Quality and Regulatory Officer to join our client’s life sciences organisation focussed on devices. This is an excellent opportunity to join an extremely varied position.
Junior Regulatory Affairs Manager - you need 3-4 years experience in regulatory - regulatory applications (CTA, Ethics and ARSAC)
Nottingham
Mar 21
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 - Beautiful and historic Ghent- Belgium- Do you have 5 -7 years regulatory experience and some Medices experience.
Belgium
Mar 21
To apply for this Regulatory Affairs role please call Julie Cooper on 07951 082482 or please send your CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Manager - Great consultancy with some remote working and flexible hours - Oxfordshire
Oxfordshire
Mar 21
To apply for this Regulatory Affairs Manager please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
SSU and Regulatory Specialist II (Slovakia)
Slovakia
Mar 21
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
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Associate Director - Regulatory Affairs - Can work remotely and flexible working hours. Great regulatory work in a company with great work ethic
Oxfordshire
Mar 21
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 Manager - Some remote working and flexible hours.Great variety of work and work for a company that is different.
Oxfordshire
Mar 21
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Global Regulatory Labelling Director - US and EU experience - Lead a team - 3 days in office and 2 remotely - Central London
London
Mar 21
To apply for this Regulatory Affairs Labelling Director please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Consultant/Manager Cambridgeshire
Cambridgeshire
Mar 21
Zest Scientific is keen to identify an experienced Regulatory Affairs Manager/Consultant/Executive from within the pharmaceutical, clinical research or biotechnology sectors. We are keen to speak with individuals with a number of years experience and are now looking to develop their career with a leading organisation in the Cambridgeshire area.
Regulatory Associate Director \ Regulatory Director
Berkshire
Mar 21
Regulatory Associate Director \ Regulatory Director Location: Berkshire Salary: Up to £90,000 + company benefits •Do you want to work for a growing specialist consultancy?
Senior Regulatory Affairs Associate
Wiltshire
Mar 21
Senior Regulatory Affairs Associate: Wiltshire •Have over 15 years sector expertise and still rapidly growing. •Are an established international pharmaceutical company with a structured and strategic growth plan.
Global Regulatory Affairs Manager - Yorkshire
Yorkshire
Mar 21
Global Regulatory Affairs Manager Location: Yorkshire Salary: £60,000 - £75,000 per annum + company benefits Do you want to work for one of the Top 10 Consumer Health companies in the world?
Regulatory Affairs Manager
Munster, Republic of Ireland
Mar 21
Our client, a global medical devices company, are currently recruiting for a Regulatory Affairs Manager. The primary function of this role is to supervise the Regulatory Affairs area to ensure that it runs in a smooth and efficient manner. Function will involve a thorough understanding of both the regulatory requirements required for the Medical Device Industry.
Global Regulatory Associate - Respiratory
Yorkshire
Mar 21
Global Regulatory Associate - Respiratory Location: Yorkshire Salary: £28,000 - £38,000 per annum + company benefits Do you want to work for one of the Top 10 Consumer Health companies in the world?
Global Senior Regulatory Associate
Yorkshire
Mar 21
Global Senior Regulatory Associate Location: Yorkshire Salary: £38,000 - £49,000 per annum + company benefits Do you want to work for one of the Top 10 Consumer Health companies in the world?
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Senior Regulatory Affairs Associate
Yorkshire
Mar 21
Senior Regulatory Affairs Associate: Yorkshire Salary: £35,000 - £45,000 + Benefits Regulatory Professionals are recruiting on behalf of a global leading company, we are seeking a Senior Regulatory Affairs Associate to be based in Yorkshire branch of the company.
Regulatory Affairs Associate
Yorkshire
Mar 21
Regulatory Affairs Associate Location: Yorkshire Employment: Permanent Salary: £28,000 - £35,000 + Benefits Regulatory Professionals are recruiting on behalf of a leading global pharmaceutical company.
Site Start Up and Regulatory Specialist - France
France
Mar 21
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
Regulatory Affairs Consultant / RA / Clinical Trial Applications
High Wycombe, London
Mar 21
Regulatory Affairs Consultant / High Wycombe/ 6 Months Contract /54 to 68 GBP (Per Hour)
Regulatory Program Manager
England
Mar 21
We currently have an opportunity for an exceptional Regulatory Programme Manager to join our global team working specifically on our Immunology/Rheumatology portfolio. The role will be based in Welwyn Garden City in the UK or in Basel. ...
Associate Director- Regulatory Affairs - Marketed Products- London/Flexi- £70,000 + Car allowance
London
Mar 20
As Associate Director for European Regulatory Affairs within a global pharma sponsor you will be tasked with providing strategic focus across the product lifecycle for marketed products within the EU, line management of a small team of regulatory professionals and to ensure collaboration with stakeholders to ensure projects meet agreed deadlines.
Regulatory Affairs Manager CMC (m/f)
Hessen
Mar 20
Regulatory Affairs Managers – CMC (m/w)Office-based in HessenJob Description:- Compose high quality, global CMC clinical (IND/CTA) and marketing applications (NDA/MAA), including authorship in some sections- Lead communications with global regulatory agencies (FDA, EMA, and others) and facilitate review and approval of submissions- Interact with management from multiple internal functional areas, corporate partners, international regulators and external experts- Lead and/or participate in cr ...
Principal Consultant - Regulatory
England
Mar 20
Genpact Pharmlink is a highly specialised Regulatory Affairs Consultancy with a successful history. The success of Genpact Pharmalink depends on its people. Capitalizing on what is unique about individuals and drawing on their different perspectives and experiences will add value to the way we do business.
Regulatory Project Manager
England
Mar 20
Genpact Pharmlink is a highly specialised Regulatory Affairs Consultancy with a successful history. The success of Genpact Pharmalink depends on its people. Capitalizing on what is unique about individuals and drawing on their different perspectives and experiences will add value to the way we do business.
Regulatory Affairs Associate (Contract)
Jersey City
Mar 20
Regulatory Affairs Associate (Contract)My client is looking to bring on a Regulatory Affairs Associate onto the team for 6-12 months. The Regulatory Affairs Associate...
regulatory jobs : 100 +
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