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The latest Regulatory jobs - BETA

Jobs: (Regulatory)

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Sr SSU and Regulatory Specialist (Russian Federation)
Russian Federation
May 23
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.
Assoc Dir, SSU Regulatory - Europe
Europe
May 23
Do you want to be a 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 ASSOCIATE 2 - Belgium and Netherlands
Mechelen, Belgium,Utrecht, Netherlands
May 23
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Regulatory Affairs Associate 2 and help realize your career potential.
Senior Manager, Regulatory Affairs Medical Devices
Ghent
May 23
A new leadership opportunity has arisen with a global Pharmaceutical company. They are currently searching for an Senior Manager, Regulatory Affairs to Lead their Medical Devices team in the Belgium. This is a novel position within the organisation which will allow for further growth and structure within the Regulatory Affairs team.
Senior Regulatory Officer - CMC
Berkshire
May 23
Senior Regulatory Officer - CMCA fantastic opportunity for an experienced Regulatory Professional to join a global CRO. You will Prepare and review CMC regulatory submissions and have CMC responsibility for a portfolio of assigned products. ...
Manager, Regulatory Affairs
Hertford
May 23
A superb opportunity has arisen for an ambitious and industrious individual to work on multiple varied projects utilising and acquiring numerous skills. You will be working with a well-established and growing consultancy within a team with an increased focus on clinical projects working with key clients.
Senior Associate CMC Regulatory Affairs
Bern
May 23
A superb new opportunity has arisen with a global market leading Biotechnology company. They are currently searching for an Senior Associate CMC Regulatory Affairs. This is a technical position within the organisation which will combine technical expertise and Regulatory Affairs team.
Associate Director, International Regulatory Affairs
London
May 23
A superb new opportunity has arisen with a global market leading Pharmaceutical company. They are currently searching for an Associate Director, International Regulatory Affairs to Lead their team in the UK. This is a novel position within the organisation which will allow for further growth of the Regulatory Affairs team.
Field actions regulatory specialist
Eindhoven
May 23
Amoria Bond is urgently looking for an Interim regulatory specialist within an established medical device company near Eindhoven.
Excellent oportunity for Senior Consultant/Consultant Regulatory Services
Budapest
May 23
Consulting Opportunities at PAREXEL Consulting jobs at PAREXEL help our client companies get and keep biopharmaceutical and medical devices on the market. Through integrated product development services, you’ll help clients maximize their product portfolio value and protect them from regulatory risk. Are you experienced in Early Stage Development, Clinical Trial Regulatory Services, Late Stage Development and Strategic GxP Compliance? Explore Consulting jobs at PAREXEL.
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Regulatory Affairs CMC Scientist
Belgium
May 23
TalentSource Life Sciences is currently searching for an experienced Regulatory Affairs CMC Scientist to join one of our biotechnology partner companies in Belgium. The Regulatory Affairs Specialist will be responsible for supporting the Global Regulatory CMA Biologics team with global regulatory submissions.   The successful candidate will be working on studies dedicated to one client.
Regulatory Affairs Specialist - global, international Company
Frankfurt ( Oder)
May 22
A unique Regulatory Affairs Specialist job for an organised Regulatory Specialist in a global operating company for Pharmaceuticals. This position offers the chance to bring...
Regulatory Submissions Analyst
South East England
May 22
Senior Regulatory Submission Analyst – Regulatory Publishing, EMEA Buckinghamshire Our client is a bold, global pharmaceutical company that is focused on developing, manufacturing and commercializing branded pharmaceuticals, devices and biologic products for patients around the world. JOB SUMMARYPublishes submissions within the EMEA (Europe, Middle East and Africa) Region in line with current national and regional requirements for eCTD, NeeS and Paper applications. ...
Associate Director Regulatory Affairs - Oncology
London
May 22
ProClinical is currently seeking an Associate Director Regulatory Affairs for an exciting job opportunity joining a leading worldwide, research-based pharmaceutical company based in London. The company has over 30,000 employees worldwide, with products that include treatments for diabetes, cancer and asthma. Job Responsibilities: Collaborates to define, develop and lead global and/or regional strategies to maximise regulatory success towards achievement of program objectives. ...
Regulatory Affairs Senior Manager and Directors needed – Immunology – Belgium - advance your career with a progressive Biotech Company
BELGIUM with Relo
May 21
If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, 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 EMEA Director Manage a team for new mAb indications and market expansion Brussels
BELGIUM with Relo
May 21
If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, 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 Associate Director Belgium Would you like to work on Biotech projects in a Global Role…
BELGIUM with Relo
May 21
If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, 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 Associate Director Based Brussels – Manage a strong RA team development and lead strategic EU MAA’s
BELGIUM with Relo
May 21
The pipeline here is what really makes the difference – there are a high number of indications in phases 1,2 and 3 so you will be well matched with a product that suits your expertise and interest in therapy area and phase of development. The culture here is one of high visibility and real product responsibility. Please send your CV with a covering note to cv@advregulatory.com or alternatively call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Director / EU and Global regulatory strategies - line management and project management role / Brussels
Belgium
May 21
My top ten pharmaceutical client based in Brusselsis looking for someone special. They seek a regulatory affairs Director with experience of both line management and project management for EU and Global projects with In-depth knowledge of Paediatric Investigation Plans and Orphan Drug Designation applications. Call Theo Moore or Matt Greig on +44 (0)207 801 3384 for full details or to apply for this role
Regulatory Affairs Director, Europe – Full project lifecycle role covering Development and EU MAA’s
Belgium
May 21
This is a hands-on role where you will have leadership of your projects, as you report into a highly engaging and experienced Head of Regulatory Affairs. As the company grows so will this role as there are strong expansion plans already in place. To apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion a call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
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Labeling Compliance and Regulatory Project Leader
Basel
May 21
Labeling Compliance and Regulatory Project Leader wanted for our Basel based client in the pharma industry. ...
Regulatory Affairs Manager
South San Francisco
May 20
Regulatory Affairs Manager - South San Francisco Reporting to the Associate Director, Regulatory Affairs, and according to the directives of the company leadership and management, and applicable regulations, established procedures and planned objectives, the Manager, Regulatory Affairs will be responsible for preparing, managing and executing regulatory activities for drug products in the US and Canada. ...
Regulatory Medical Writer
Richmond
May 20
Regulatory Medical Writer - RemoteThe scope of this position includes the writing, coordination and oversight of clinical deliverables including clinical study protocols, protocol amendments, and clinical study reports, Investigator’s Brochures, clinical contributions to briefing documents and annual safety reports as well as other IND/NDA/CTA or global regulatory submission documents. ...
Regulatory Affairs Manager
Richmond
May 19
Manager, Regulatory Advertising and Promotion - Richmond, VANote: For the right candidate, remote working will be considered.The Manger, Regulatory Advertising and Promotion is a skilled regulatory manager with strong understanding of the FDA regulations associated with Ad/Promo 21 CFR Part 202.1 (Prescription Drug Advertising) and possesses excellent review and editing ability. Understanding safe and effective use of drug products for human consumption. ...
Quality and Regulatory Manager
Munich
May 19
I am looking  for a permanent Quality & Regulatory Manager based in Germany; Munich:The Company ·         Global leading provider of innovative solutions·         Building...
Regulatory Affairs Assistant
Leeds
May 19
Our Client, a leading Medical device business is currently looking a Regulatory affairs assistant in Yorkshire for a 12 month project.
Regulatory Affairs Associate CMC - international mid size Company
Munich
May 19
A fantastic Graduate Regulatory Affairs Job opportunity for an excellent communicative Junior Regulatory Manager CMC to join an international growing pharmaceutical company. This position offers...
Associate Director Regulatory Affairs - innovative mid-size Pharma
Munich
May 19
A unique Associate Director Regulatory Affairs job for an organised Senior Regulatory Manager or Associate Director Regulatory Affairs to join a global operating company for...
Junior Regulatory Affairs Manager - you need 3-4 years experience in regulatory (CTA, Ethics and ARSAC)
Nottingham
May 19
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Manager - Great consultancy with some remote working and flexible hours - Oxfordshire
Oxfordshire
May 19
To apply for this Regulatory Affairs Manager please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
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Regulatory Affairs Manager - Some remote working and flexible hours.Great variety of work and work for a company that is different.
Oxfordshire
May 19
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 - Work 2 days remotely - Central London
London
May 19
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 Director - Denmark- Flexible hours and some remote working
Copenhagen
May 19
To apply for this role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Manager - Great consultancy with some remote working and flexible hours - Oxfordshire
Oxfordshire
May 19
To apply for this Regulatory Affairs Manager please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
TMF Manager, Regulatory Records
England
May 19
Do you want to be a 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.
Strategic Client Manager, Regulatory Records
England
May 19
Do you want to be a 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.
Associate Director Regulatory Affairs - innovativer Mittelstand
Munich
May 19
Eine einmalige Gelegenheit Ihre Kompetenzen aus Regulatory Affairs und Emerging Markets in einem innovativen Unternehmen einzubringen und das Wachstum weiter auszubauen. Sie arbeiten bei einem...
Regulatory Associate II CMC
Cambridge
May 19
Regulatory Associate II CMC - CambridgeJOB SUMMARY:i-Pharm Regulatory have a Regulatory Affairs Associate II position which will focus on supporting Global CMC . 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. ...
Senior Manager Global Regulatory Affairs - Herts
Hertfordshire
May 19
Oliver Care is recruiting for a Senior Regulatory Affairs Manager within Emerging Markets to join a company in the pharmaceutical industry at their site based...
Director, Regulatory and Site Services
United Kingdom,Belgium,France,Germany,Italy,Netherlands,Portugal,Spain,UK - London,UK - SouthWest,UK - Midlands,UK - SouthEast,UK - NorthWest,UK - NorthEast,UK - Scotland,UK - Wales,UK - Northern ...
May 19
Excellent opportunities to develop your career in this growing department - home or office based - UK or EU
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Regulatory Affairs Senior Project Manager
San Francisco
May 18
Skills Alliance is partnered with a leading global biotech in San Francisco to secure an experienced Project Manager within Regulatory Affairs. The Regulatory Affairs Senior...
CMC Regulatory Affairs Director
Macclesfield
May 18
CMC Regulatory Affairs Director - UK - Macclesfield At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. ...
Regulatory Affairs Leader
Berlin
May 18
Regulatory Affairs Leader (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 und externer F ...
Regulatory CMC Manager, Advanced Therapies
Cambridge
May 18
A superb new opportunity has arisen with a leading Regulatory consultancy. They are currently searching for a CMC specialist within their Advanced team in the UK. This is a vital position within the organisation which will provide CMC expert input into Regulatory submissions globally.
Manager Regulatory Affairs (m/f)
Villingen-Schwenningen (78052)
May 18
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 ...
Senior Regulatory Affairs Manager Munich (m/f) Permanent
München (81249)
May 18
Senior Regulatory Affairs Manager Munich (m/f) PermanentI am currently searching for the next Senior Regulatory Affairs Manager for a leading International organisation within the healthcare industry, based in Munich.The role gives the responsibility of managing and enforcing EU & National regulatory strategies.
Manager, Regulatory Advertising and Promotion (REMOTE)
Remote - Home Based
May 18
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at 617 982 1238 today!
Strategic Client Manager, Regulatory Records
England
May 18
Do you want to be a 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.
Specialist or Senior Specialist - Global Regulatory Affairs
Home based, Europe
May 17
Specialist or Senior Specialist - Global Regulatory Affairs permanant home based any Europe country to support activities due to new projects with regulatory oversight to clinical studies awarded to Worldwide across regions for all stages of the drug development cycle (from phase I to IV). Experience in Global submission is required.
Regulatory Affairs Officer
England
May 17
6 MONTH CONTRACT - Regulatory Affairs Officer – Pharma South-East England Competitive Salary To start ASAP
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Regulatory Labelling Manager (m/f) in the Area of Zug
Zug
May 17
Regulatory Labelling Manager (m/f) in Baar Our clients is an internationally leading Medical Technology Company who offers an exciting tailored career path for your professional and personal development within their Regulatory Affairs & Quality Assurance team. The client is specialized on heart diagnosis, monitoring as well as software solutions. The manufacturing takes place in Switzerland and the products are distributed worldwide. ...
Interim Regulatory Affairs / field safety specialist
Eindhoven
May 17
Amoria Bond is urgently looking for an Interim regulatory specialist within an established medical device company near Eindhoven.
Senior Regulatory Affairs Associate
Slough
May 17
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. Our vision: We strive to be the leading supplier using science and technology to improve the quality of life. ...
Regulatory Affairs Professional - Various levels considered
Hertfordshire
May 17
Regulatory Affairs Professional - Various levels considered Location: Hertfordshire Salary: £40,000-£75,000 dependant on experience Would you like the opportunity to gain experience in both EU and US territories?
Associate Director, Regulatory Affairs
Princeton, NJ
May 17
Under the direction of regulatory affairs management, the incumbent independently prepares and directs global regulatory affairs activities and provides regulatory guidance during drug development, approval and post approval processes and commercialization, in coordination with both the internal and external consultants and contractors in the oncology therapeutic area.
Associate Director, Regulatory Affairs – CMC
Princeton, NJ
May 17
Under the leadership of the Director/Senior Director, CMC Regulatory Affairs the incumbent manages the global regulatory CMC activities except Asia for all projects, provides strategic CMC regulatory guidance during drug development, approval, post approval, and commercialization, in coordination with internal staff and external consultants/contractors.
Regulatory Affairs Officer - Compliance (France)
France
May 16
Regulatory Affairs Officer - Compliance (France) Reference: J28643 Location: France Salary: Up to €38,000 + Great Benefits An opportunity has arisen to become part of one of the largest generics companies in the world.
Senior Regulatory Affairs Manager
England
May 16
An established company in drug development are researching, studying, manufacturing & making society aware of the benefits of a new drugs. They are looking for an individual with broad experience within Reg Affairs to work on range of tasks on Growth Markets.
Regulatory Executive - GRAD Reg
England
May 16
We are working with a specialist pharma consultancy based in Hertfordshire who are looking for a new member to come on board & be trained as a Reg Executive. They"e;re forward thinking & take time to understand individual needs & find creative solutions for any challenge.
Regulatory Affairs Specialist
Paris
May 16
ewi Life Sciences are partnering with a global brand to find them a Regulatory Affairs Specialist.The company design and manufacturer a wide range of medical devices which are distributed globally to improve the life of patients everywhere.I am looking to speak with Regulatory Affairs professionals who are already based in France or European Citizens who would consider living near the French Capital. ...
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Regulatory Affairs Manager (m/w) - Freiberuflich/Freelance
Germany
May 16
Regulatory Affairs Specialist (m/w) - FreiberuflichFreelanceHome – basedEin internationales Pharma Unternehmen sucht zum nächstmöglichen Zeitpunkt einen Freiberufler Regulatory Affairs für ein Projekt bis zum Sommer 2019 mit 0.6 FTE. ...
Site Start Up and Regulatory Specialist - Spain
Spain
May 16
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 Officer / RA
Beerse, Belgium
May 16
Regulatory Affairs Officer / Beerse, Belgium/ 6 Months Contract / 25 EUR (Per Hour)
Associate Manager Regulatory Affairs-140249
Europe, Middle East and Africa-Bulgaria-Sofia-Sofia
May 16
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. ...
Associate Director/Director CMC Regulatory Affairs - Boston
Boston / Cambridge
May 15
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
Regulatory Affairs Manager - San Fran
bay area
May 15
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 MA
May 15
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
Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
May 15
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
Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
May 15
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
Associate Director, Global Regulatory Affairs; Immuno-Oncology
USA
May 15
For more info please call Sam Murphy on 0044 208 544 3423 / sam.murphy@tecgroup.net
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Regulatory Affairs Officer (Clinical Trials)
England
May 15
Do you have 2-3 years' experience in classic Regulatory Affairs or 6-12 months Clinical Regulatory Affairs experience and are looking to pursue your Global Clinical Trials Regulatory experience? This opportunity will allow you from your first week in to support global Clinical Trial Applications and take leadership of projects suited to your level. Apply now for instant consideration!
Regulatory Affairs Manager
Nürnberg
May 15
My client in Nurnberg, Germany is searching for a new regulatory affairs manager. They are a medical technology company that provides materials and products with...
Regulatory Clinical Manager - Medical Devices
Antwerp
May 15
Regulatory Clinical Manager - Medical Devices - Consultancy
Freelance Regulatory Affairs Specialist (m/w) - Teilzeit
Germany
May 15
Pharma Freelance Regulatory Affairs Specialist (m/w) - TeilzeitFreiberufler/ FreelancerHome - basedIhre Aufgabe• Regulatory Advice für die Zulassung• Erstellen aller nötigen Dokumente für die internationale Zulassung• Direkter Ansprechpartner für Behörden und Ämter• Interne und externe Anfragenbearbeitung der RA Richtlinien• Organisation des internen EntwicklungsprozessesIhre Qualifikation• Relevantes Studium oder Vergleichbare Arbeitserfahrung• Senior Erfahrung in der Zulassungen von Produk ...
Home Based – Regulatory Writer – Global CRO
England
May 15
This world leading CRO is after experienced medical writers who can come in 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
Finland
May 15
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.
Senior Analyst Regulatory Affairs - Permanent - Munich, GERMANY
London
May 15
*Regulatory Affairs Analyst** Permanent**Munich, Germany* I am currently looking for a Senior Analyst Regulatory Affairs for a permanent position working with a Medical Device company to be based in Munich, Germany.DescriptionWorking within the Workflow and Informatics Solutions Business Unit (WITS) Design Quality & RA organization, the Senior Analyst Regulatory Affairs assures regulatory requirements are met for new product introduction and design changes to established products. ...
Regulatory Affairs Assistant / RA / Medical Devices
Leeds
May 15
Regulatory Affairs Assistant / Leeds /12 Months Contract / 14 to 17 GBP (Per Hour)
Regulatory Consultant - 6 Months - Medical Device
Hertfordshire
May 14
I am looking for a RA Specialist for a 6-9 months’ contract for a Medical Device Company in Hertfordshire. They are looking for someone to start as soon as possible and can interview this week.Job Role: Experience in preparing in STEDRisk ManagementDesign ReviewsChange ControlMaintenance of Tech FilesSTED – new SOPProcedural writing Keywords:Medical Device, Medical Devices, 13485, Regulatory, RA, 510K Files, CE Marking, Reg, STED, Technical File
OPTION BELGIQUE Director Regulatory Affairs Lead a Team 6 FTEs on new indication, market expansion, Biological Major Blockbuster
BELGIUM with Relo
May 14
You may be working as a matrix leader, or full direct manager, either in a CRO or within a pharmaceutical company. You may be working on a mix of products, and now want to focus and consolidate your lifecycle (including new indications) experience. You will be ready to embrace change and want to work in a leadership team which is visionary, has what it takes to turn the word innovation in to something a regulator will sign up to!
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Regulatory Director and Associate Director Roles in Oncology (mAbs) – Become a GRL or Lead a Team - Salaries range from 100-165K Euros
The Netherlands - full relocation and sign-on Bonus
May 14
My client is seeking individuals who are ready or at Associate Director or Director level, want to work on both complex EU and / or global product development strategies in Oncology and want a career which can either encompass team management in time or GRL status - To apply for this role, please send your CV with a covering note to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Director – EMEA strategy and Team Leading Role – Great Salary and Package - Brussels
BELGIUM with Relo
May 14
This role is a good mix of strategic input, global project management and covers early and late-phase development for a strong therapeutic franchise with a great mix of products. You will need enormous drive and enthusiasm, with the ability to inspire your team and the wider group to perform / achieve to a higher level. 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.
OPTION BELGIQUE: Global Regulatory Team Leader ... Director or Associate Director, 38+10 days off, Car, Stock and Relocation
BELGIUM with Relo
May 14
This position is the pivot between the GRLs and Commercial teams, and the regulatory professionals who will report in to you. This will mean you will plan, oversee and lead the individuals on specific projects and tasks, ensuring support to the franchise for critical submissions, which includes for Centralised products for the European region, as well as extended international regions (MENA, CIS to Turkey and CE & E).
Regulatory Affairs Director for Immunology Franchise - Lead Strategy and Development and EU MAA’s + Lead a strong team of regulatory performers
BELGIUM with Relo
May 14
Operate as the Regulatory lead for a Global Brand in Immunology - Lead the development and Implementations of regulatory strategies for MAA’s within the EMEA region - Identify future commercialisation opportunities for worldwide markets - Manage strong team of regulatory performers. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs EMEA Team Leader – Join a growing biotech in a Strategic RA role for EMEA MAA activities – Brussels
Belgium
May 14
As the EMEA Regulatory Team Lead you will play a pivotal role in providing support to the GRL with respect to mentoring & leading the team for all types of submissions and strategic initiatives. If you wish to apply for this role please click below, or send your CV with a covering note to cv@advregulatory.com quoting reference number noted above or call Theo Moore or Matt Greig on +44 207 801 3380
Regulatory Affairs Director - GRL role for Oncology - The Netherlands - Salary to 150,000 + Bonus + Car (Full Re-location package available)
The Netherlands, close to Amsterdam and Leiden
May 14
My International pharmaceutical client is looking for a talented Regulatory Affairs Director to provide strategic & operational support to Global & regional based project teams for both development & Life-cycle management projects in Oncology. You will also have at least 10 years experience of hands on European regulatory activities in a matrix environment and be looking for a highly visible position. Contact Theo Moore or Matt Greig on +44 (0) 207 801 3384 or email CV@AdvRegulatory.com
OPTION BELGIQUE Director Regulatory Affairs Lead a Team 6 FTEs on new indication, market expansion, Biological Major Blockbuster
BELGIUM with Relo
May 14
You may be working as a matrix leader, or full direct manager, either in a CRO or within a pharmaceutical company. You may be working on a mix of products, and now want to focus and consolidate your lifecycle (including new indications) experience. You will be ready to embrace change and want to work in a leadership team which is visionary, has what it takes to turn the word innovation in to something a regulator will sign up to!
Regulatory Submissions Coordinator - Lyon, France
Lyon, France
May 14
Our client is a Global CRO working across various Drug and Device Therapeutic areas and Indications. With endless opportunity and continuously growing clientel, there is extensive internal growth and progression.
REGULATORY in ATLANTA, GA Sr Regulatory Manager(s) and Associate Director(s) NEW Opportunities Growing bio-/pharma Relocation Offered
ATLANTA
May 14
You want to work in a location where there is high nett to cost of living ratio (more disposable income once the bills are paid), a warmer climate, and where housing stock is much more affordable, and spacey!
REGULATORY Sr Regulatory Managers With Relocation Choice of 2 TAs, incl. mABs Be mentored in to GRL positions RTP or GA USA
RTP, SC or GA USA or Home Working
May 14
The company offer an advantageous package, including 20% bonus, Health Insurance, Savings plan and mid points which are high for their States in terms of Nett salary to Cost of Living, and moreover the ability to gain a clear ladder to become a GRL in the future, based on your merit and achievements.
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Manager, Regulatory Affairs
United States
May 13
home or office based in the U.S.
Senior Regulatory Affairs Manager - Great consultancy with some remote working and flexible hours - Oxfordshire
Oxfordshire
May 12
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 (Serbia)
Serbia
May 12
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 Manager Disposables
Baden-Württemberg
May 12
Regulatory Affairs Manager Disposables (m/w)Office-based in Baden – Württemberg Aufgaben:- Zuarbeit von Entwicklungsprojekten- Strategieentwicklung und Prüfung von Zulassungen- Schnittstelle zwischen den einzelnen Fachbereichen- Prozessoptimierung- Durchführung von Schulungen mit normativem Hintergrund- Erstellung der technischen DokumenteVoraussetzungen:- Kenntnis in der Zulassung von Disposables- Abgeschlossenes Studium mit technischem Hintergrund- Kenntnisse mit medizinischen Produkten- K ...
Global Regulatory Labelling Director - US and EU experience - Want freedom to work a couple of days remotely Central London
London
May 12
To apply for this Regulatory Affairs Labelling Director please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Near beautiful Canal City GHENT - Regulatory Manager - Medical Devices - NPD , Strategy and Compliance - International role
Belgium
May 12
To apply for this role please call Julie Cooper on 07951 082482 or alternatively send your CV in the strictest confidence to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - you need 3-4 years experience in regulatory - (CTA, Ethics and ARSAC) Create and review documentation
Nottingham
May 12
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Manager - Great consultancy with some remote working and flexible hours - Oxfordshire
Oxfordshire
May 12
To apply for this Regulatory Affairs Manager please call Julie Cooper on 07951 082482 or 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
May 12
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
May 12
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 jobs : 100 +
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