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The latest Regulatory jobs

Jobs: (Regulatory)

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Senior Regulatory Consultant Home-Based
England
Jan 22
The CompanyOur client, a multinational CRO are seeking a Senior Consultant to join their expanding team in the United Kingdom. This position can either be office based or home-based.The PositionAs the new Senior Regulatory Affairs Consultant, you will be responsible for product and portfolio management. This includes but is not restricted to, Life-cycle maintenance, variations, renewals and the market expansion of products.As part of the remit you will also: * Lead large scale projects. ...
Senior Manager of Regulatory Affairs in London
London
Jan 22
Global Biotechnology company looking for their next Senior RA Manager or RA Manager...
Senior Regulatory Writer | Regulatory Writer | Medical Writer |
Massachusetts
Jan 22
Senior Regulatory Writer | Regulatory Writer | Medical Writer | CRO | Massachusetts One of the world’s leading, full-service ophthalmic CRO’s are looking to speak with Regulatory Writers who are looking to take a step up into a senior position. Location: Home/Office based – MassachusettsAbout the position:As the Senior Regulatory writer, you will be in charge of researching, writing and editing materials for all Regulatory Submissions. ...
Director, Regulatory Writing | Massachusetts | Regulatory
Massachusetts
Jan 22
Director, Regulatory Writing | Massachusetts | RegulatoryLocation: Home based i-Pharm Consulting have partnered with the world’s leading independent, full-service ophthalmic clinical research and product development firm.With offices, globally, our client support a wide array of organizations, from start-ups to global pharmaceutical and device companies. ...
Senior Manager Regulatory Affairs
London
Jan 22
My client, a Global Pharmaceutical Company, has opened a new vacancy within their Regulatory team and are actively looking to recruit a Regulatory Affairs Senior Manager. The role will be based at my client’s offices in Central London. The Role: The Regulatory Affairs Snr Manager provides regulatory support and expertise on assigned programmes, and is responsible for specific pieces of moderately complex projects. ...
Regulatory Affairs Manager (m/w) Office-based in Hamburg-Süd
Hamburg
Jan 22
Mein Kunde ist ein forschendes und produzierendes Medizintechnikunternehmen mit Sitz bei Hamburg, das einen starken Werdegang hinter sich hat und nun einen Betrieb mit prall gefüllter Pipeline und spannenden Produktinnovationen darstellt.
Associate Director - Regulatory Affairs
London
Jan 22
Associate Director - Regulatory AffairsLocation: LondonDuration: 6 monthsHours: 37.5 per weekTravel: Some international travel may be required (20%)
Regulatory Affairs Graduate
Petersfield
Jan 22
ProClinical is currently advertising on behalf of a fabulous British healthcare company that offers a range of medicines, medical devices, diagnostics and OTC products.The company is currently seeking an Administrative Reporting Line to join their UK-based team.The incumbent will provide full administrative support for the company’s Regulatory Affairs activities. ...
Regulatory/Medical Affairs/Quality and Compliance Manager
Dublin, Republic of Ireland
Jan 22
On behalf of our client, a Dublin based pharmaceutical company, we are currently recruiting for a Regulatory/Medical Affairs/Quality & Compliance Manager. This role will be based in their local commercial affiliate. The candidate will be responsible for supporting the commercial team in achieving business objectives by managing regulatory approvals and ensuring the compliance of company products with local regulations and internal procedures.
Regulatory Affairs Specialist/Manager
Dublin, Republic of Ireland
Jan 22
On behalf of our client, a global pharmaceutical company, we are currently recruiting for a Regulatory Affairs Specialist/Manager
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Senior Medical Writer Regulatory - Home-based
Home-based
Jan 22
Asha Mistry of Umbilical Life is recruiting a Medical Writer for a global CRO based in the UK.
Medical Writer Regulatory - Home-based
Home-based
Jan 22
Asha Mistry of Umbilical Life is recruiting a Medical Writer for a global CRO based in the UK.
CMC Regulatory Manager in Hertfordshire
Hertfordshire
Jan 22
Laura Durrell is recruiting for a CMC Regulatory Manager to join a multinational clinical-stage cell & gene therapy research company focused on the development and...
Senior Regulatory Affairs Specialist.
Limerick
Jan 21
On behalf of my client, a multinational medical device company, I am recruiting for a Senior Regulatory Affairs Specialist.
Regulatory Affairs Manager in High Wycombe
High Wycombe
Jan 21
Mary Bolt at CK Clinical is recruiting for a Regulatory Affairs Manager to join a company in the pharmaceutical industry at their site based in...
Regulatory Affairs Director
Limerick
Jan 21
On behalf of my client, a  global medical devices company , I am recruiting for a Regulatory Affairs Director to join their Irish operation.
Senior Regulatory Affairs Associate in High Wycombe
High Wycombe
Jan 21
Mary Bolt at CK Clinical is recruiting for a Senior Regulatory Scientist/Associate to join a company in the pharmaceutical industry at their site based in...
Regulatory Affairs CMC Manager
Rep. Ireland
Jan 21
On behalf of my client we are sourcing a candidate for the role of Regulatory Affairs CMC Manager.   This is a permanent role.
Regulatory Affairs Officer
Rep. Ireland
Jan 21
On behalf of our client, a leading pharmaceutical company based in the South-East of Ireland, I am recruiting for a Regulatory Affairs Officer.
Regulatory Affairs Officer
Belgium
Jan 21
Regulatory Affairs Officer, BelgiumAn exciting opportunity has arisen to join a leading CRO and manage their regulatory activities. You will be involved in a wide variety of exciting projects and clinical trials. ...
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Senior Director, Regulatory Affairs
New Jersey
Jan 21
The CompanyOur Client, a leading pharmaceutical organisation is seeking a Senior Director of Regulatory Affairs to join their organisation in the U.S. office.The PositionAs the Senior Director of Regulatory Affairs, you will serve as a representative for a variety of projects in Oncology, Autoimmune diseases or Respiratory therapeutic areas. ...
Regulatory Labelling Officer
North London
Jan 21
Regulatory Professionals are now collaborating with a Global Animal Health Company who specialise in high quality medicines for control diseases in livestock and companion animals.
Regulatory Labelling Associate
North London
Jan 21
A internationally recognized Animal Health company who specialize in the development of veterinary pharmaceutical products seek a Regulatory Labelling Associate on a contractual basis.
Medical / Regulatory Writer
Middlesex
Jan 21
If you’ve got a solid background in regulatory or clinical medical writing and you’d like to hear about a great role with a well established and highly regarded research based pharma company I’d love to hear from you. Our client is a research based EU pharmaceutical company with a fantastic reputation both from a product perspective and as a place to work. With a range of well established and innovative pipeline products they have a balanced portfolio and enjoy consistent growth. ...
Regulatory and Compliance Global Director Based UK, BeNeLux QMS and PI for the global regulatory function With Relocation
UK M4 or BeNeLux
Jan 21
You will see yourself as someone who can provide solutions into the value chain, by working with different sub teams, different functions and in a role where you will report to the senior management team member (the global RA leadership team), for an individual with a truly remarkable reputation >>>
EUROPE Senior Regulatory Manager Have you worked on a line extension and now want to work on a new MAA With Relocation
Mainland Europe
Jan 21
We are pleased to present you this role for a major bio-pharmaceutical company, where both the ideas of the GRL career pathway and working on a new MAA are part of this opportunity. You will be joining a successful company in a smaller team to focus on filing a MAA with multiple indications and will directly work with the GRL who is highly experienced and much liked.
EMEA Regulatory Liaison - High Wycombe
High Wycombe
Jan 18
Steve Lord at CK Clinical is recruiting for an EMEA Regulatory Liaison to join a company in the Pharmaceutical industry at their site based in...
Senior Regulatory Affairs Manager
Hamburg
Jan 18
Description: A leading medical device consultancy is in search of Regulatory Affairs Manager located in the North of Germany. The organisation seeks to offer services for all regulatory affairs and process optimisation of quality management and quality systems. As a company, with over 30 years of experience, they excel within all regulatory and normative issues regarding the approval of medical device, quickly and efficiently. ...
Regulatory Affairs Specialist
Swindon
Jan 18
This globally recognised organisation specialises in designing, developing and manufacturing skin contact solutions for the Healthcare and Medical Devices sector.
Director of Regulatory Affairs
England
Jan 18
Director of Regulatory Affairs - Global Bio-Pharma - Oxford
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Regulatory Affairs Manager; Top Biopharma; Emerging Markets/ROW/International; Regulatory Strategy, Central London location
London
Jan 18
Regulatory Affairs Manager; ROW/Emerging Markets focus; Strategy and Affiliate liaisons; Project Managing; Top Biopharma; Great London location
Regulatory and Public Affairs Lead HC Provider Central Europe Relo and Housing Allowance Build Reg Intell with Public Affairs
Central Europe
Jan 18
To apply or enquire, please contact me, Matt Greig, on UK +447918679405 or send me a full CV to matt@advregulatory.com and I will contact you by return. I am available for telephone calls after work all week, if this is easier, on the same number.
Senior Regulatory Affairs Specialist
Leuven
Jan 18
A unique career opportunity has arisen at MedTech Professionals. We are working with one of the worlds most established and well-respected Medical Devices companies
CMC Regulatory Manager / Senior Manager Early to late, IMPDs, to MAA/BLA authoring Develop into a GRL for CMC in time, Pure Dvlpt role
West of London, M4 Corridor
Jan 18
Do you see yourself as someone who overtime wants to develop into a strategy leading role? This is an opportunity to go into a pure development role, so you will be in the right place to gain this experience. The role is based within easy commute of West London, Berkshire, Middlesex, and South Bucks.
Senior Regulatory Affairs Associate (Clinical Submissions)
Uxbridge, England,United Kingdom
Jan 18
As part of a multi-national project team, you will help to coordinate the compilation, review and submission of regulatory agency applications for local projects in compliance with regulatory requirements as well as internal and client standard operating procedures (SOPs). Your knowledge of clinical trial regulations will enable you to support the team for the development of optimized clinical trial submission strategies. ...
Regulatory Affairs Snr Project Manager – EU and then Global role covering early and late stage dev. projects to CeP leadership
Brussels, Belgium
Jan 17
This is a rare opportunity where you can grow and develop to be the lead for both EU and US markets, for large molecules in a medium sized organization with a flat structure that likes to give regulatory staff the opportunity to reach their potential. Contact Theo Moore on +44 (0) 207 801 3384 or email me in confidence via theo@advregulatory.com
Regulatory CMC Senior Manager Want to gain more region, be promoted and developed and work in a quickly expanding biotech Switzerland
Switzerland
Jan 17
New position to support a pipeline of biological products, with several assets in early development, 1 in global submission and 1 in preparation for BLA, yes, the role is global and includes both the EU and USA. To apply, please contact either myself Oli on +44 (0)20 7801 3388 or my colleague Theo Moore on +44 (0)20 7801 3384 or send a full CV to cv@advregulatory.com and we will respond by return.
Regulatory Manager / Senior RA Manager Join EU MAA team, part of 1st MAA Bio then co-lead 5 new indications Novel MOA Relo Offered
BeNeLux
Jan 17
My client is a well-known bio-pharmaceutical company with a strong pipeline and a stable environment, seeking individuals who want to get ahead in their career, individuals who will apply themselves in order to grow and learn. You will consider this role ...
OPTION BELGIQUE Sr / Regulatory Programme Manager EU and GRL Career Pathway No mature products GAIN RA Dev and NEW Lifecycle
Belgium
Jan 17
This role will appeal to individuals who want to work in a Global HQ where 70% of ALL decisions are made in the same building! This role is based in Belgium, comes with an attractive salary, bonus, and a great deal of opportunity to grow. This company has a track record of developing individuals from Manager and Senior to the Global Regulatory Lead level!
Regulatory Affairs EU Project Manager Work on Bio dev. projects and lead MAA`s Great Training Available
Belgium
Jan 17
A major Belgium based pharmaceutical company are seeking a regulatory affairs professional with 3 to 8 years pharmaceutical experience with knowledge of regional regulatory procedures and legislation to work on EU and sometimes global Biological development projects leading to MAA. This role comes with excellent training and real career development opportunities. Call Theo Moore or Matt Greig TODAY on +44 (0)207 801 3380 or send your Cv in confidence to CV@AdvRegulatory.com
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Director Regulatory Affairs und Qualitätsmanagement (m/w) - BW
Germany
Jan 17
Mein Kunde ist Teil einer globalen Unternehmensgruppe mit Fokus auf den Dental-Bereich und sucht zum nächstmöglichen Zeitpunkt eine Führungskraft für den RA&QM-Bereich.
Medical Device Clinical and Regulatory Consultant- Germany- Home Based
Germany
Jan 17
My client, an international medical device focused CRO are seeking an experienced regulatory consultant. 
Senior Regulatory Affairs Manager
Central London / West End
Jan 17
An exciting opportunity has arisen within an innovative pharmaceutical company specialising in Oncology.
Regulatory Affairs Director
Nottingham
Jan 17
A fantastic opportunity has arisen within an expanding bio-tech specialising in an exciting, niche product that enables better therapies for patients worldwide.
Senior Regulatory Affairs Associate (CMC biologics)
Uxbridge, England,United Kingdom
Jan 17
PAREXEL Consulting is looking for Senior Regulatory Associate with CMC biologics expertise.A Senior Associate must be technically competent and continually developing the skills as defined in the responsibilities section of this document. A Senior Associate, under the general direction of a Project Lead and Technical SMEs, takes responsibility for ensuring that client work is performed, and delivered on time, meeting the quality expectations of PC and the client. ...
Senior Regulatory Associate (CMC lifecycle maintenance)
Uxbridge, England,United Kingdom
Jan 17
This role specifically will support primarily one of PAREXEL's large partnerships in the life cycle maintenance of a product portfolio.A Senior Associate must have an understanding of the organization’s basic consulting models and methodologies, as well as basic knowledge of what services PARXEL Consulting provides.A Senior Associate must be technically competent and continually developing the skills as defined in the responsibilities section of this document. ...
Regulatory CMC Consultant
Republic of Ireland
Jan 16
The CompanyOur client, a multinational CRO are seeking a Regulatory CMC Consultant to join their expanding team based in Ireland.The PositionAs the new Regulatory CMC Consultant, you will be responsible for product and portfolio management. This includes but is not restricted to, life-cycle maintenance, variations, renewals and the market expansion of products.As part of the remit you will also: * Lead large scale projects. ...
Senior Regulatory Writer
Massachusetts
Jan 16
The CompanyOur client, a multinational CRO are seeking a Senior Regulatory Writer to join their expanding team in Massachusetts, US.The PositionAs the new Senior Regulatory Writer, you will be expected to author and review regulatory documentation, with the main focus being on clinical study reports (CSR) and clinical study protocols. You will also assist in the writing of patient narratives and investigator brochures (IB). ...
Global Regulatory Lead (Home-Based)
Central London / West End
Jan 16
We are working with a leading Clinical Research Organisation to appoint a Global Regulatory Lead.
Senior Regulatory Executive in Ware
Ware
Jan 16
Jenni at CK Group is recruiting for a Senior Regulatory Executive to join a company in the Pharmaceutical industry at their site based in Ware...
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Regulatory Senior Executive 75509
Hertfordshire
Jan 16
My Client a Global Pharmaceutical Company has opened a new vacancy within there Regulatory team and are looking to recruit a Senior Regulatory Executive - CMC on a 6 month contract basis to be based at their offices in Hertfordshire.
Regulatory Affairs Consultant (Clinical and Labeling)
Bucharest, Bucure ti,Romania
Jan 16
We are currently looking for an experienced Consultant (Clinical and Labeling Lifecycle management)A Consultant must have an understanding of the organization’s consulting models and methodologies, as well as, good knowledge of what services PAREXEL Consulting provides. A consultant must have strong technical skills and may be developing specialist knowledge of a particular subject and/ or market. ...
Senior Consultant - Regulatory Outsourcing Projects
United Kingdom
Jan 16
PAREXEL Consulting is looking for a Senior Regulatory Affairs Consultant in the UK or in Dublin. The purpose of the role is to provide leadership for regulatory outsourcing projects. About the group:Functional outsourcing: CMC, Labelling, Publishing, Regulatory Information Management system maintenance.Product/Portfolio Management (post-approval support): Life-cycle Maintenance, – variations, renewals, market expansion of marketed products. ...
Senior Consultant Regulatory Affairs
High Wycombe
Jan 15
ProClinical are recruiting on behalf of a leading consultancy organisation who have a vacancy for a Senior Consultant in Regulatory Affairs. In this role, you will be working for a company that offers excellent consulting services, with a dynamic and growing team of highly qualified consultants. This job offers an annual income of £65,000, and is based in High Wycombe. ...
Senior Director of Regulatory Affairs
Central London
Jan 15
Have you ever dreamed of being part of something much bigger? A company where you are genuinely helping save lives every day, or maybe even just getting involved right at the beginning of a technology that will have proven life-altering abilities for people who have suffered for so long? Then I might just have the solution for you.
Regulatory Submissions Manager
Central London
Jan 15
Why would you want to take on someone else’s project halfway through, when you could get in at the start of something and see it grow?
Regulatory Affairs Officer / Associate
London
Jan 15
What is your target Therapy area?  Oncology? Gastro-intestinal? Anti-infection? Well… it doesn’t matter.  Not because your targets aren’t important, but because this incredible company has such a wide reach, the chances are that your favourite Therapy area is covered.
Regulatory Affairs Consultant
Stuttgart
Jan 15
ProClinical is pleased to advertise for a regulatory affairs specialist position within the medical device sector based near Stuttgart. This exciting position is contracted and will last for an initial 6 months. ...
Regulatory Systems Associate in Slough
Slough
Jan 15
Mary Bolt at CK Clinical is recruiting for a Regulatory Systems Associate to join a leading consumer health and hygiene company, at their site based...
Regulatory Affairs Specialist (m/w) in der Schweiz
Switzerland
Jan 14
Regulatory Affairs Specialist (m/w) Schweiz Mein Kunde ist ein Schweizer Medizintechnik-Hersteller und sucht zum nächstmöglichen Zeitpunkt einen Regulatory Affairs Spezialisten (m/w) für internationale Zulassungen. ...
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Regulatory Affairs Assistant in Leeds
Leeds
Jan 14
Jenni Woolley is recruiting for a Regulatory Affairs Assistant to join a company in the Pharmaceutical industry at their site based in Leeds on a...
Associate Director Regulatory Affairs EMEA (Oncology)
High Wycombe
Jan 14
Jenni at CK Group is recruiting for an Associate Director Regulatory Affairs EMEA to join a company in the Pharmaceutical industry at their site based...
Title: Sr Regulatory Affairs Manager Do you want to be part of a major MAA filing In a company with the GRL pathway available Mainland EU
Mainland Europe
Jan 14
Summary: We are pleased to present you this role for a major bio-pharmaceutical company, where both the ideas of the GRL career pathway and working on a new MAA are part of this opportunity. You will be joining a successful company in a smaller team to focus on filing a MAA with multiple indications and will directly work with the GRL who is highly experienced and much liked.
Senior Regulatory Affairs Associate - based in Dublin or Bucharest
Dublin, Leinster,Ireland
Jan 13
The role is based either in Dublin or Bucharest.The successful applicant will work as a Product Lead with a team for one of PAREXEL Consulting's large partnership clients to perform post marketing CMC activities and respond to inquiries from HA or the client. ...
Junior Regulatory Affairs Associate - based in Dublin or Bucharest
Dublin, Leinster,Ireland
Jan 12
The role can be based in our Dublin or Bucharest office.The main focus of the role is to provide support for administrative CMC activities included update to RtQ tracker, LDR updates, form updates, CPPs – activities will be QC’d where required by SME.QualificationsLife science degreeBasic regulatory experience would be nice to have but not necessary for right candidate who has worked in the industry and is willing to learnAbility to interact and co-ordinate activities with a team. ...
Regulatory Affairs Consultant - based in Dublin or Bucharest
Dublin, Leinster,Ireland
Jan 12
The successful applicant will serve as the technical coordinator on one of PAREXEL Consulting's large partnership projects. The technical coordinator will be responsible for the successful handling of all RA matters for a specific product portfolio. The role is office based in Dublin or Bucharest. ...
Regulatory Affairs Consultant (CMC)
Bucharest, Bucure ti,Romania
Jan 12
PAREXEL values passion, global perspective and expertise and we are in the process of recruiting full time, permanent Regulatory Affairs Consultant (CMC focused) to join our PAREXEL Consulting team in Bucharest. PAREXEL Consulting offers services which create and maximize product value for clients throughout the product lifecycle, leveraging our unique fusion of scientific, regulatory, and business expertise. ...
Regulatory Consultant - Tadworth, Surrey
Tadworth
Jan 11
Jenni at CK Group is recruiting for a Regulatory to join a company in the pharmaceutical industry at their site based in Tadworth, Surrey on...
Regulatory Consultant in Tadworth, Surrey
Tadworth
Jan 11
Lucy Stendall at CK Group is recruiting for a Regulatory Consultant to join a company in the Pharmaceutical industry at their site based in Tadworth,...
Regulatory Consultant (part remote working)
Remote working / Surrey
Jan 11
12 month reg affairs contract for experienced regulatory consultant in MA renewals/variations/applications with opportunity to work from home 2 days a week - based in South East - competitive rates of pay
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Regulatory Affairs Specialist – CMC
Dublin, Republic of Ireland
Jan 11
On behalf of our client, a global pharmaceutical company, we are currently recruiting for a Regulatory Affairs Specialist – CMC
Senior Regulatory CMC Manager
Hatfield
Jan 11
Regulatory Professionals are working with a research-based pharmaceutical company who are currently looking for a Senior CMC Regulatory Manager.
Manager Regulatory Affairs (m/w)
Tuttlingen
Jan 11
Mein Kunde ist ein forschendes und produzierendes Medizintechnikunternehmen mit Sitz in Stuttgart und sucht zum nächstmöglichen Zeitpunkt einen erfahrenen Zulassungsexperten (m/w).
Senior Regulatory Affairs Manager in Stevenage
Stevenage
Jan 11
Mary Bolt is recruiting for a Senior Regulatory Affairs Manager to join a multinational clinical-stage cell & gene therapy research company focused on the development...
Regulatory Affairs Junior Submissions Manager München (m/w)
Germany
Jan 11
Für unseren Kunden aus München sind wir aktiv auf der Suche nach einen Junior Submissions Manager für die Regulatory Affairs Abteilung. Sie werden für die Einreichungen in eCTD Format auf einer globalen Ebene verantwortlich sein. Sie werden die Möglichkeit haben sich in neuen Gebieten weiterzuentwickeln. Zusätlich zu den flexiblen Arbeitszeiten bietet das Unternehmen einen überdurchschnitlichen Gehaltspaket an. ...
Regulatory Affairs Associate - 1 year fixed term contract (renewable)
Madrid, Madrid,Spain
Jan 11
PAREXEL values passion, global perspective and expertise and we are in the process of recruiting a Regulatory Affairs Associate to join our PAREXEL Consulting team in Madrid. PAREXEL Consulting offers services which create and maximize product value for clients throughout the product lifecycle, leveraging our unique fusion of scientific, regulatory, and business expertise. ...
Quality and Regulatory Lead - Medical Devices
Sydney
Jan 10
JOB SUMMARYA Quality and Regulatory Lead is required for a small but growing medical devices company building their global operation from Sydney.The company has recently had a large capital injection globally providing an exciting phase in their growth.
Regulatory Affairs Executive
Berkshire
Jan 10
An exciting opportunity has become available for an experienced and enthusiastic Regulatory Affairs Executive / Senior Regulatory Officer, to join an exciting new client based in Berkshire! The successful candidate will have a strong background in registration and post approval submissions, and ideally a background within generics.
Regulatory Affairs Scientist - Growing Consultancy
Surrey
Jan 10
Regulatory Affairs Scientist - Growing Consultancy - UK Based
Regulatory Affairs Executive
Maidenhead
Jan 10
A start up pharmaceutical client is looking for a Regulatory Affairs Executive on a permanent basis. The role is focused on submitting applications via NP and the ideal candidate would be responsible for mentoring junior regulatory team members as well as liaising with relevant regulatory authorities. The role is based in Maidenhead and salary is paying up to £40,000.
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Regulatory Submission Manager
Dublin
Jan 10
On behalf of my client, a leading Pharmaceutical company, I am recruiting for a Regulatory Submission Manager. This is a permanent role available within Dublin. within the Regulatory Submission Management Department in Dublin.
Manager (m/w) Regulatory Affairs
Baden-Württemberg
Jan 10
Manager (m/w) Regulatory Affairs Mein Kunde ist ein forschendes und produzierendes Medizintechnik-Unternehmen mit Sitz in Baden-Württemberg und sucht zum nächstmöglichen Zeitpunkt einen erfahrenen Regulatory Affairs Manager (m/w). ...
Regulatory Affairs Manager Europe and ROW / Emerging Markets / International - based in Ireland
Cork, Ireland
Jan 10
Regulatory Affairs Manager; Ireland location; Registrations & Post marketing; EU & International/ROW/Emerging Markets; Project managing
Regulatory Affairs Director in Nottingham
Nottingham
Jan 10
Laura Durrell at CK Clinical is recruiting for a Regulatory Affairs Director to join a pharmaceutical company based in Nottingham on a permanent basis.The...
Senior Regulatory Affairs Manager, Oncology in Uxbridge
Uxbridge
Jan 10
Mary Bolt at CK Group is recruiting for a Senior Regulatory Affairs Manager - Oncology, to join a world leading pharmaceutical company at their site based...
Senior Regulatory Affairs Manager, General Medicine in Uxbridge
Uxbridge
Jan 10
Mary Bolt at CK Group is recruiting for a Senior Regulatory Affairs Manager - General Medicine, to join a world leading pharmaceutical company at their site...
Senior Regulatory Affairs Consultant
Buckinghamshire
Jan 10
Within this role you will provide regional regulatory support for one or more products, and as a member of the EU Oncology Regulatory Team.
Regulatory Manager UK Affiliate
London
Jan 10
An exciting opportunity has arisen for a Regulatory Manager to join a global biopharmaceutical company based in London. A very patient-focused company, who scientific research has resulted in 15 marketed products that are benefitting hundreds of thousands of people, a pipeline of late-stage drug candidates and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. ...
Senior Regulatory Associate
Uxbridge
Jan 10
ProClinical is currently recruiting for a Senior Regulatory Associate job at a leading multinational biopharmaceutical company with leading therapies in autoimmune diseases and oncology. They are seeking an individual to bring solid regulatory affairs experience their team at their offices in Uxbridge. This is an exciting opportunity to work for one of the world's biggest biotechnology firms that employs over 17,000 staff globally. ...
Regulatory Affairs Manager
Aylesbury
Jan 10
Here is a chance to join one of the most globally known pharmaceutical organisations, who is looking to hire a Regulatory Affairs Manager based in Buckinghamshire on a contract basis. This job will be working a top 10 pharmaceutical company that works across a range of industries from medical devices to pharmaceutical and consumer goods, operating in over 60 countries. ...
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Regulatory CMC Consultant
London
Jan 10
ProClinical is working with a global healthcare company that is seeking a Regulatory CMC Consultant to be based in London on a permanent basis. This CMC role will be project managing and providing regulatory support to assigned tasks. The incumbent will be ensuring compliance with international regulatory requirements is maintained whilst delivering on the company strategy.Job Responsibilties: * Provide regulatory guidance and advice for assigned projects/tasks. ...
Head of Regulatory Affairs | Medical Devices | IVD Products
North East England
Jan 10
A global IVD company are seeking a Head of Regulatory Affairs [READ ON]...
Associate Director, Regulatory Affairs
USA
Jan 10
Our client is a fast growing clinical stage biotechnology business which is making great strides in combating some of the most difficult neurological diseases afflicting children.
Regulatory Affairs Project Manager (m/w)
Germany
Jan 10
Wegen Expansion sucht unser Kunde nach einem Regulatory Affairs Projekt Manager für eine Vollzeit Festanstellung Office-Based in München.Sie werden haupsächlich für die Organisation von den Meetings mit den regulatorischen Behörden verantwortlich sein. Für diese Position müssen Sie über fließende Englischkenntnisse sowie Erfahrung im internationalen regulatorischen Umfeld mit Fokus auf EU und USA verfügen. ...
US Regulatory: Based RTP, NC OR Remote RA Manager or Senior Regulatory Manager Support complex lifecycle strategies, Line Extensions on mAbs
Remote, Relocate or work in RTP, NC
Jan 9
Work remotely with regular visits to the HQ, or you can already commute to RTP, Raleigh-Durham, North Carolina, or relocate to RTP, which is offered and well-funded by our client.
Regulatory Affairs Consultant
High Wycombe
Jan 9
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 6 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.Key Responsibilities/Requirements: * Preparing and submission of Regulatory documents. ...
Regulatory Affairs CMC Biologicals Senior Manager Global role covering EU and US development Based in Geneva
Geneva, Switzerland
Jan 9
My client is a highly rated and extremely successful Biotechnology company with a Global reach. They are seeking a Regulatory Affairs CMC Senior manager role covering global CMC regulatory strategies for assigned development and marketed products with a focus on creativity and innovation, maximizing the business benefit balanced with regulatory compliance. This is varied and highly strategic CMC role within the global Head office.
Regulatory Affairs CMC GRL, Director Level - This a gloabl role with a growing company in a beautiful part of the world
Geneva, Switzerland
Jan 9
My client is a Geneva based Global Biotechnology company who are looking for a bright and ambitious professional to take the lead on developing global regulatory CMC strategies for early phase projects through global registrations. Contact Theo Moore on + 44 (0) 207 801 3384
Regulatory Affairs Director
England
Jan 9
The CompanyOur client, a global pharmaceutical company are looking for a Regulatory Affairs Director to join their internationally expanding team based in the UK.The PositionAs the new Regulatory Affairs Director, you will be accountable for leading the development and implementation of global regulatory strategy for a group of products, ensuring this strategy is designed to deliver rapid approval. ...
Senior Manager, Regulatory Affairs Strategy
Welwyn
Jan 9
Regulatory Professionals are collaborating closely with a large pharmaceutical company based in Hertfordshire who are looking for a couple of Senior Managers to join their therapeutic teams.
regulatory jobs : 100 +
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