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Jobs: (Regulatory)

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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...
Senior Medical Writer - Regulatory - Switzerland
Basel
Jan 14
Our client is a Bio Pharma who are full of colour and creative edge, their R&D pipeline is full, and they have a bright future ahead of them. To be part of this very exciting journey please contact harriet.lawford@secrecruitment.com or call me for a confidential conversation on +44 207 255660 This is an exciting opportunity to join an innovative Bio pharma in Switzerland who are creative and bursting with ideas.
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. ...
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...
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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
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.
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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.
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). ...
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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. ...
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]...
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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. ...
Regulatory Affair Manager Medical Devices
Germany
Jan 10
Description         : Regulatory Affairs Specialist     : Ettlingen, Germany   Start: ASAP       TalentSource Life Sciences, the division of CROMSOURCE dedicated to flexible staffing solutions, is currently recruiting for a Regulatory Affairs Specialist to strengthen the team of one of our TOP Pharmaceutical client Companies in Ettlingen, Germany.
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 and Compliance Global Director Based UK, BeNeLux QMS and PI for the global regulatory function With Relocation
UK M4 or BeNeLux
Jan 9
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 >>>
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. ...
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 9
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.
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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 Affairs Manager (CMC) - Biotech
Germany
Jan 8
Boisimilars development
Senior Regulatory Manager
Hatfield
Jan 8
An incredible opportunity for a Senior Regulatory Affairs Manager with a UK/Ireland focus to join a leading and extremely reputable Pharmaceutical company with a phenomenal portfolio.
Regulatory Affairs Officer
Ipswich
Jan 8
Regulatory Professionals are collaborating with a Premier Bio-Pharmaceutical company who are looking for a Regulatory Affairs Officer to join their growing team
Senior Regulatory Affairs Associate - UK home based
Reading, or home based in UK
Jan 8
PRA Health Sciences are a Clinical Research Organisation committed to developing our people. We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.
Senior Regulatory Manager
Central London / West End
Jan 8
Regulatory Professionals are currently working with an innovative pharmaceutical company with focus in Oncology.
Senior Regulatory Affairs - REMOTE
England
Jan 8
I am currently assisting a client with a Senior Regulatory position - the client are leaders in the Life Sciences Industry and are looking for the ideal Consultant to have the following experience.Overview: * IVD/IVDR Experience * Technical Files * Conducting Gap Assessments * Validation - Documentation * Specific Regulatory Project ManagementThe client would be interested in a Consultant to Permanent opportunity if both parties are keen - further down the line. ...
Regulatory Affairs Officer I
Reading
Jan 8
Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
Senior Regulatory and Start-Up Specialist (f/m) - office based in Frankfurt or Freiburg/Br.
Freiburg or Frankfurt
Jan 8
Senior Regulatory and Start-Up Specialist with focus on country level RSU tasks (contract management, approvals, submissions to EC) Full-time office-based in Freiburg or Frankfurt
Senior Regulatory Affairs Specialist (contract)
Belgium
Jan 7
Senior Regulatory Affairs SpecialistAn amazing opportunity to work within the Regulatory Affairs department of a Leading Global Life Sciences Company has become available. You will be working at a Consultant level, overseeing the regulatory strategy for a portfolio of products. ...
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USA Sr Regulatory Strategist NBEs with Biomarkers for Precision Medicines Create the vision Precision Meds offers Patients East Coast
East Coast
Jan 7
You will lead from different Project teams, acting as, as is the case with regulatory folks a lot of the time, the bridge between research and clinical, to co-shape or define the regulatory pathway, with specific biomarkers and accompanying diagnostics, being integrated into the CDP and RA strategy, for selective / predictive and continuous biomarkers and their accompanying diagnostics.
ONCOLOGY Regulatory Associate Director Ready to step up to US Liaison role Offers velocity of filings Relocation Offered US East Coast
Tri-State US East Coact
Jan 7
You will see yourself as a rising star, because of your work ethic, ability to translate detail into cogent filing plans and submissions, and now feel the time is right to break out of ‘assisting’ your current senior team members, to you yourself, having more accountability and responsibility, and maybe this is just not available where you are currently
Manager Regulatory Affairs (m/w)
Niedersachsen
Jan 7
Manager Regulatory Affairs (m/w) Office-basedNord-West Mein Kunde ist ein forschendes und produzierendes Medizintechnikunternehmen und sucht zum nächstmöglichen Zeitpunkt einen erfahrenen Zulassungsexperten (m/w). ...
Regulatory Affairs Officer
Belgium
Jan 7
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. ...
ONCOLOGY (Sr) Regulatory Director Have solid full project lifecycle and now want to work in pure development US East Coast with Relo
Tri-State
Jan 7
You might be working in a smaller company covering the full regulatory lifecycle or have had your focus change to be more on lifecycle and are missing the cut and thrust of supporting regulatory submissions for clinical studies and resulting NDAs/BLAs, either way it will be great to hear from you. The company is offering 3 distinct advantages ...
Regulatory Project Manager Oncology An opportunity to Shine US East Coast with Relo Build the track record towards the GRL career pathway
Tri-State
Jan 7
In return for your energy, dedication and existing regulatory project management capabilities, my client is offering a great starting point, a relocation package if needed which includes house purchase / sale, and a competitive package and bonus package and health insurances. My client allows 3 days in, 2 days out ... Please Click in for more information.
Regulatory and Start-Up Specialist
Tel Aviv
Jan 7
Direct, manage and perform tasks at country level associated with Regulatory, Start-Up (RSU) and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. Manage Regulatory and Start-up (RSU) team(s) and overall activities, where applicable.
Regulatory Affairs Project Manager
England
Jan 7
Award winnig CRO - IQVIA is pleased to announce open vacancy. As REGULATORY AFFAIRS PROJECT MANAGER you will be expected to lead a broad cross-functional Core Transition team, comprised of functional representatives appropriate for the deal. SU will act as the Patient Safety Regulatory Affairs lead a broad cross-functional Core Transition team.At IQVIA™ your work will also impact healthcare around the world as you will be involved with the most important drugs and the highest-profile clients.
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 4
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.
Regulatory RIM Consultant
Oxford
Jan 4
ProClinical is seeking a Regulatory RIM Consultant for a UK based biotechnology company. This position will provide Global Regulatory Affairs Operations support for Regulatory Information Management (RIM) system and associated activities. Job Responsibilities: * Works closely with project team to update RIM system. * Manage the transfer of data from old EDMS to current RIM system. ...
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Senior Regulatory Affairs Associate
England
Jan 4
The CompanyOur Client, a global bio pharmaceutical organisation, which has acquired some exciting new company’s over the last number of years, is seeking a Senior Regulatory CMC Associate.The PositionAs the new Senior Associate, you will report into the Regulatory Affairs Manager and be responsible for preparing quality sections of INDs/IMPDs, new MAAs, CMC variations and renewals for submission in EU. ...
Senior Regulatory Affairs Associate - CMC
England
Jan 4
The CompanyOur client, a global Bio-pharmaceutical company are seeking a Senior Regulatory CMC Associate to join their team based in the UK.The PositionAs the new Senior CMC Associate, you will be responsible for preparing the quality sections of Clinical Trial Applications, Marketing Authorisations, Variations and Renewals. As part of the remit you will also: * Co-ordinate the preparation of responses to CMC questions from regulatory authorities. ...
Senior Regulatory Affairs Manager, UK and Ireland in Cambridge
Cambridge
Jan 4
Laura Durrell is recruiting for a Senior Regulatory Affairs Manager - UK and Ireland to join a privately owned Pharmaceutical company bringing innovative medicines to UK...
Regulatory Operations
Cambridge
Jan 4
Regulatory Professionals are collaborating with a global bio-pharmaceutical company with a strong pipeline including treatments for cancer and respiratory disease treatments.
Data Reporting – Regulatory Affairs (m/f) - Freelance (6Months)
Frankfurt am Main
Jan 4
Freelance Project (6 Months)Data Reporting – Regulatory Affairs (m/f)Office-based in Greater Frankfurt Do you have experience as a Data Reporting (m/f) with knowledge in Regulatory Affairs? Are you a Freelancer and are you looking for a new project? Then this is the right job for you!The Company: My client is a well-known international company in the pharmaceutical industry. ...
Associate Director Regulatory Labelling in Hertfordshire
Hertfordshire
Jan 3
Laura Durrell at CK Clinical is recruiting for an Associate Director Regulatory Labelling to join a global pharmaceutical company committed to contributing to better healthcare...
Regulatory Affairs Manager
Sweden
Jan 3
Reg Affairs Manager. Uppsala, Malmo or Stockholm. Permanent. Full Service CRO
Manager Regulatory Affairs (m/w) Office-based Baden-Württemberg
Stuttgart
Jan 3
Manager Regulatory Affairs (m/w) Office-basedBaden-Württemberg Mein Kunde ist ein forschendes und produzierendes Medizintechnikunternehmen mit Sitz in Stuttgart und sucht zum nächstmöglichen Zeitpunkt einen erfahrenen Zulassungsexperten (m/w). ...
Regulatory Affairs Manager
Edinburgh
Jan 3
Regulatory Professionals are working with an international pharmaceutical company who are looking to bring on board a new Regulatory Manger.
Senior Regulatory Affairs Project Manager in High Wycombe
High Wycombe
Jan 3
Lucy Stendall at CK Group is recruiting for a Senior Regulatory Affairs Project Manager to join a company in the Pharmaceutical industry at their site...
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Regulatory and Public Affairs Lead HC Provider Central Europe Relo and Housing Allowance Build Reg Intell with Public Affairs
Central Europe
Jan 3
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.
Regulatory Affairs Specialist - Medical Device
Switzerland
Jan 3
This position is responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level for the EMEA region. Primary responsibilities are to ensure regulatory compliance for assigned product lines as the company evolves.
Regulatory Medical Writer - Home based
London
Jan 3
An excellent opportunity has arisen for an experienced Regulatory Writer to join a growing CRO based in London. This role will offer the rare chance to either work remotely from home, or in the office.
Head of Regulatory Affairs (m/w) - bei Hamburg
Hamburg
Jan 3
Mein Kunde ist ein forschendes und produzierendes Medizintechnikunternehmen mit Sitz bei Hamburg und sucht zum nächstmöglichen Zeitpunkt einen erfahrenen Zulassungsexperten (m/w), der/die die entsprechende Abteilung leitet und ein Team führt.
Manager Regulatory Affairs (m/w) - Hamburg
Hamburg
Jan 3
Manager Regulatory Affairs (m/w) - Office-based bei Hamburg
Regulatory Affairs Specialist
Chippenham
Jan 3
A very exciting opportunity for a Regulatory Affairs Specialist has come up, to join a leading and extremely reputable Global Pharmaceutical company with a huge dominance within Life Sciences.
Director, Regulatory Affairs - Pharma
Switzerland
Jan 3
The Director of Regulatory Affairs is responsible for directing, planning, and implementing all regulatory operations for products, line extensions, licensed products etc. This includes regulatory strategies for new product registration and submission of appropriate regulatory filings.
Senior Associate Regulatory Affairs
England
Jan 2
Contract Senior Regulatory Affairs Associate
Regulatory Affairs Consultant
Sweden
Jan 2
Contract Regulatory Affairs Consultant
Regulatory Operations Manager (Publishing)
England
Jan 2
We've had an exciting position released working with a London based global biotechnology company. As our client is currently expanding, they're seeking a Senior/ Regulatory Operations Manager to join the team. You'll have the chance to work on CTA and MAA submissions across EMEA.
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Regulatory Affairs Consultant
Belgium
Jan 2
Regulatory Affairs Consultant An amazing opportunity to work within the Regulatory Affairs department of a Leading Global Life Sciences Company has become available. You will be working at a Consultant level, overseeing the regulatory strategy for a portfolio of products. ...
Regulatory Affairs Snr Project Manager – EU and then Global role covering early and late stage dev. projects to CeP leadership
Brussels, Belgium
Jan 2
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 2
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 2
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 ...
Senior Regulatory Affairs Specialist (Medical Devices)
Hertfordshire
Jan 2
I am currently working with a very well established Medical Device company who are looking for a Permanent Senior RA Specialist to join the team based in Hertfordshire.The key responsibilities of the RA Specialist will include: Establish, manage and maintain good relationships with the local regulatory authorities in the regionInteracts directly with regulatory authorities personnel and coordinate post-market surveillance activities, for all business units. ...
Regulatory Affairs Officer
Ipswich
Jan 2
A leading pharmaceutical organisation are actively looking for a Regulatory Affairs Officer to join their established team due to a project back fill.
OPTION BELGIQUE Sr / Regulatory Programme Manager EU and GRL Career Pathway No mature products GAIN RA Dev and NEW Lifecycle
Belgium
Jan 2
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 2
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
Regulatory Affairs CMC Expert home-based
England
Jan 2
The CompanyOur client, a global Contract Research Organisation are seeking a fully-home based Regulatory CMC Expert to join their global network of over 300 regulatory professionals.The PositionAs the new Regulatory Affairs CMC Expert, you will be responsible for providing up to date and comprehensive original and translated regulatory documentation, expert country summaries and regulatory information covering operational details. ...
Regulatory Affairs Medical Device Expert home-based
England
Jan 2
The CompanyOur client, a global Contract Research Organisation are seeking a fully-home based Regulatory Medical Device Expert to join their global network of over 300 regulatory experts.The PositionAs the new Regulatory Affairs Medical Device Expert, you will be responsible for providing up to date and comprehensive original and translated regulatory documentation, expert country summaries and regulatory information covering operational details. ...
regulatory jobs : 100 +
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