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The latest Regulatory jobs

Jobs: (Regulatory)

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GMP Quality/Regulatory Compliance Manager
Mayo, Ireland
Aug 14
On behalf of our client, a contract research organization, I am recruiting for a GMP Quality/Regulatory Compliance Manager. This is a permanent role within the Biologics division. 
OPTION SUISSE Regulatory CMC Director Pure mAbs and Team Management role Development and Marketed, US and Europe and Int’l Majors
Switzerland
Aug 14
OPTION SUISSE ** Regulatory CMC Director *** Pure mAbs & Team Management role ** Development & Marketed, US and Europe & Int’l Majors? This role is based in Switzerland, within easy commute of Lausanne, Geneva, or Bern. The role comes with an advantageous package including RSUs.
OPTION SUISSE Regulatory CMC Leader Biologicals Live Work Ski in this great location working for an expanding biotech Relo Offered
Geneva - with Full Relocation
Aug 14
The position comes with full support for moving and relocation, and a high level salary and bonus, as well as the normal Swiss benefits. This role is open to any European or US candidate, who has worked on EU or US submissions for regulatory CMC biologicals as a CMC RA Bio Lead, has submitted at least 1 major MAA or a set of major variations, and now wants to move to a global role.
QA Systems Officer Contract Have you supported CAPAs for PhV and Regulatory Systems 6 months ROLLING
Belgium
Aug 14
We have a 16 week contract role for a Global Regulatory Compliance Officer with an expanding Pharmaceutical company based in Brussels, Belgium. If you wish to apply for this role, please send your CV with a covering note to oli.dimitrov@advregulatory.com or alternatively, call Oli in the London office on +44 (0)20 7801 3388.
Regulatory Affairs Manager
Surrey
Aug 14
My client a leading pharmaceutical firm have an urgent Regulatory Manager contract vacancy to be based from their Surrey offices.
Regulatory and Site Services Specialist - Portugal
Lisbon
Aug 14
We are looking to recruit Regulatory and Site Services Specialist office based in our Chiltern Office in Portugal to Support the RSS team.
Regulatory and Site Services Specialist
Portugal
Aug 14
We are looking to recruit Regulatory and Site Services Specialist office based in our Chiltern Office in Portugal.
Senior Regulatory Affairs Manager
Hertfordshire
Aug 14
This leading global research and development pharmaceutical company is looking for a senior regulatory affairs manager to join their Hertfordshire team.
Associate Manager Regulatory Affairs, Rest of World (ROW) Marke
Cambridge
Aug 13
Associate Manager Regulatory Affairs, Rest of World (ROW) MarketsHours per Week : 37.518 months contractRate: £35 to £40 per hour Start date: as soon as possible.Job Description:This position is in the ROW Markets Team, which provides regulatory support to the company activities in markets outside of the EU/US; more specifically within the Asia Commercial comprised of HK/Macau, SG, Malaysia, Korea, Taiwan and China regional team.
Regulatory Database Manager - Issy Les Moulineaux
Issy Les Moulineaux
Aug 13
Laura Durrell at CK Clinical is recruiting for a Regulatory Database Manager to join a company in the pharmaceutical industry at their site based in...
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Regulatory Affairs Specialist - Oberdorf, Switzerland
Oberdorf B L
Aug 13
Jocelyn Blackham is recruiting for a Regulatory Affairs Specialist to join a global organisation, specialising in the development of medical devices at their site based...
Regulatory Consultant - Biosimilars
Germany
Aug 10
Fully home based position with occasional travel on site after an initial onboarding week for a large pharma in Germany.
Regulatory Affairs Asssociate
Essex
Aug 10
A small bio-tech based near the Hertfordshire/Cambridgeshire border are currently going through a period of growth and therefore require a Regulatory Affairs Associate.
Senior Regulatory Affairs Manager
Cambridge
Aug 10
Regulatory Professionals are working with one of the worlds leading biotechnology companies.
Regulatory Sciences Associate - Entry level
Seer Green, Nr Beaconsfield, Buckinghamshire
Aug 9
A full time opportunity to work in a thriving regulatory consultancy, providing support for regulatory submissions and post authorisation in line with agreed client strategy. The role requires the ability to collect data relevant to essential regulatory questions, issues and problems and identify factors leading to regulatory recommendations.
Senior Specialist CMC Regulatory Affairs - Biosimilars - CDMO
Gdansk
Aug 9
An excellent opportunity for an ambitious Regulatory Affairs specialist to join a fast paced and rapidly emerging, Global Biosimilars Manufacturing/Pharma Company at their new facility in Poland. This role works closely with organisations in the EU where they are partnered with further R&D and Clinical Development specialists within the world of Biosimilars.
Senior Regulatory Specialist
Hull
Aug 9
A highly reputable and expanding medical devices company based in the east of Yorkshire are seeking a Senior Regulatory Affairs Specialist to join their new product development team.
Regulatory Affairs Manager - Exciting Global Biopharma, Sussex/South England – upto £70,000 + Bonus + Benefits
West Sussex
Aug 9
We are a growing Global Biopharma going through an exciting period of growth and we are now recruiting for an experienced Regulatory Affairs Manager to champion change, provide full oversight of the regulatory function, work on international projects and lead a team of regulatory professionals. This is a really exciting opportunity offering excellent career development and work-life balance.
Regulatory associate
Essex
Aug 8
Regulatory Professionals are collaborating with a specialist pharmaceutical company who focus on developing medicines that target diseases with unmet medicinal needs.
Regulatory Associate - London
Uxbridge
Aug 8
Julie Marshall is recruiting for a Clinical Trial Application to join a company in the Pharmaceutical industry at their site based in Uxbridge on a...
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Regulatory Affairs Associate - 74248
Middlesex
Aug 8
Our client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Affairs Associate on an initial 6 month contract to be based in their offices in Middlesex
Regulatory Affairs - UK and IRE Contractor
London
Aug 8
A biopharmaceutical client based in London is looking to hire an experienced contractor focused on UK affiliate level regulatory affairs.The organisation is a top tier biopharmaceutical organisation famed for bringing medicines to market which have significantly improved patients lives around the globe.Candidates must have excellent exposure to post marketing regulatory activities and extensive MHRA/HPRA interactions and significant ABPI code of practice review for promotional materials. ...
International Regulatory Strategy- CPP Coordinator
London
Aug 8
ProClinical has a new role for a coordinator to work with our International Regulatory team, full job title: International Regulatory Strategy, CPP Coordinator.This is an admin role where the candidate will need experience within the pharma industry but not necessarily within regulatory. However the role will be working with regulatory bodies so excellent attention to detail is required. ...
Freelance Regulatory Affairs Artwork Specialist (m/w)
Germany
Aug 8
Regulatory Affairs Labeling Specialist (m/w) FreelanceDeutschland0,4 FTE2-3 Monate Aufgaben: * Verantwortlich für die Prüfung sowie Korrektur von Artwork * Eingabe von den relevanten Informationen in die Datenbank * Ansprechspartner für die interne AbteilungenProfil: * Abgeschlossenes Studium der Biologie/Chemie/Pharmazie oder verwandte Bereiche abgeschlossene Berufsausbildung im pharmazeutischen Umfeld (z.B. ...
Regulatory Project Manager
Cambridge
Aug 8
This leading pharmaceutical firm seeks an experienced Regulatory Project Manager to join their established team in a contract position until the end of the year.
Regulatory Affairs Specialist- Publishing- All EMEA Locations-148829
Europe, Middle East and Africa-Bulgaria-Sofia-Sofia,
Aug 8
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. ...
Regulatory Affairs Manager (ATMP)-149259
Europe, Middle East and Africa-UK-England-Cambridge,
Aug 8
PPD has opened this fantastic opportunity to join our Regulatory Affairs department as a Regulatory Affairs Manager based in the EMEA region. In this role, you will act as subject matter expert in providing regulatory strategy advice to internal and external clients. ...
Regulatory Affairs Specialist - Inverness, Scotland
Inverness
Aug 7
CK Group is recruiting for three Regulatory Affairs Specialists to join a company in the Medical Devices industry at their site based in Inverness on...
Regulatory Affairs Product Specialist
London
Aug 7
Our client, a global biotechnology company that employs over 20,000 people across the world, is looking to hire a Regulatory Affairs Product Specialist. The company specialise in creating breakthrough therapies for rare diseases and works to produce an innovative pipeline across their key therapy areas. ...
Regulatory Affairs Specialist – South East – 3 months
England
Aug 7
RA Specialist - 3 months Full job description and company details are available upon application, apply below. This position is being dealt with by Matt Lowe-Lauri at meet, call on +44 (0) 2030195988 or email directly at matthew@peoplewithchemistry.com to discuss in confidence.
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Regulatory Affairs Specialist
Scotland
Aug 6
If you’re an existing Regulatory Affairs professional looking for a challenging new opportunity, it would be great to talk to you about a new role I’m handling based in Scotland.I’m working with a leading UK Pharmaceutical company looking to recruit a Regulatory Affairs Specialist.You will be responsible for providing Regulatory leadership for global regulatory affairs. As well as having a body of Regulatory Affairs experience you will also have experience with Medical devices. ...
Regulatory Affairs Specialist/Senior/Principal - EMEA-148606
Europe, Middle East and Africa-UK-England-Cambridge,
Aug 4
PPD currently has opportunities for Regulatory Affairs Specialist/Senior/Principal Specialist.   In this role you will provide regulatory advice and carry out projects in the provision of regulatory affairs services.  You will also act as liaison with internal and external clients in the provision and marketing of regulatory affairs services. ...
Associate (Graduate) Regulatory Publisher - London office based
Central London (Aldwych)
Aug 3
As an Associate Regulatory Publishing Specialist, you will be dedicated to one of our pharmaceutical clients with a truly global presence; this unique industry-changing partnership redefines collaboration. The program is ideal for individuals who thrive in a continually-evolving culture that mirrors PRA’s commitment to career development.
Regulatory Affairs Global Lead
High Wycombe
Aug 3
Regulatory Professionals are collaborating with a global pharmaceutical company who specialise in exciting and unique products.
Regulatory Affairs Senior Manager
Hertford
Aug 3
Regulatory Professionals are collaborating with a global pharmaceutical company who specialise in Oncology and Neurology products.
Senior Regulatory Affairs Associate
West London
Aug 3
Regulatory Professionals are collaborating with an exciting global Bio-pharma company who specialise in life threatening diseases.
Senior Regulatory Affairs Manager
Hertfordshire
Aug 3
This leading global research and development pharmaceutical company is looking for a senior regulatory affairs manager to join their Hertfordshire team.
Regulatory Affairs Specialist
Buckinghamshire
Aug 2
This ever expanding medical device organisation seeks an experienced Regulatory Affairs Specialist to join their established team based from their office in Buckinghamshire.
Regulatory Affairs Specialist
Buckingham
Aug 2
Regulatory Professional are currently collaborating with a rapidly growing medical device company based in High Wycombe.
Regulatory Affairs Specialist
Buckinghamshire
Aug 2
A rapidly expanding medical device company are seeking a Regulatory Affairs Associate/Specialist to join their team.
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Principle Regulatory Consultant
Hertfordshire
Aug 2
Regulatory Professionals are working with an award winning Regulatory Consultancy based in Hertfordshire.
Freelance Regulatory Affairs Leader - Surrey
Surrey
Aug 2
Just Pharma are working on behalf of a Global Pharmaceutical company supporting with their search for an experienced Regulatory Affairs Leader to cover a 12 month Maternity leave on a freelance Contract basis. ...
Regulatory HUB Labelling Manager
Surrey
Aug 2
My Client a Global Pharmaceutical Company has opened a new vacancy and is looking to recruit a Regulatory HUB Labelling Manager on an initial 12 Month contract to be based at their offices in Surrey.
Regulatory Senior Project Manager
Berkshire
Aug 2
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Senior Project Manager for Western Europe Area to be based in their offices in Berkshire.
Director Project Management (FSP), Regulatory Affairs and Pharmacovigilance support for Established Products-148371
Europe, Middle East and Africa-United Kingdom, Europ
Aug 2
This is an opportunity for an experienced Project Manager to join our Functional Service Partnership (FSP) team focussing on PPD's expanding Global Regulatory Affairs and Pharmacovigilance portfolio with a focus on Established Products.   The role will work effectively across multiple functional areas to direct the delivery of FSP projects within quality, time, and cost requirements. ...
Principle Regulatory Consultant
Hertfordshire
Aug 1
I am currently collaborating with a prestigious business with an excellent reputation for staff satisfaction, personal development and working flexibility.
Regulatory Affairs Specialist EMEA – Medical Devices
Elstree
Aug 1
The role of the Regulatory Affairs Specialist EMEA – Medical Devices is to maintain responsibility for all regulatory aspects of the Conformity European (CE) marking process for medical devices.
Senior Regulatory Specialist
London
Aug 1
Regulatory Professionals are currently working with a long standing and established CRO with global a presence.
Regulatory Manager
Scotland
Aug 1
Regulatory Professionals are collaborating with a research-based life sciences company with special strengths in biotechnology.
Regulatory associate II
Slough
Aug 1
Regulatory Professionals are collaborating with a global CRO who specialise in early phase clinical stage.
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Regulatory Affairs Lead
Surrey
Jul 31
This internationally recognized pharmaceutical organisation seeks an experienced Regulatory Affairs Lead to join their established team on a 12 month maternity leave cover.
Regulatory and Start-Up Specialist, Junior RSU Specialist or Senior RSU Specialist (f/m) - office based in Basel
Basel
Jul 30
We currently have an exciting job opportunity as (Senior) Regulatory Start-up Specialist (f/m) to work in our Regulatory & Start-up Department in Basle.   PURPOSEPerform tasks associated with Regulatory, Start-up (RSU) and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May participate in feasibility and/or site identification activities. ...
Regulatory Affairs Director - Cambridge
Cambridge
Jul 30
Mary Bolt at CK Clinical is recruiting for a Director Regulatory Affairs to join a global, science-led biopharmaceutical business at their site based in Cambridge...
Graduate Data Analyst - Regulatory Information - 6month FTC
Aldwych, London
Jul 30
At PRA we’re optimistic that, individually and collectively, we can help make tomorrow better than today. We believe that it is our obligation as a company to help our people find meaningful ways to respond to the needs of others around the world. This sense of common purpose pervades our culture and serves as the foundation of who we are. Explore our career opportunities today and find out how you can be part of it.
Regulatory Specialist
United Kingdom
Jul 28
This is a great opportunity for someone with a good grounding in these subjects and tasks
Senior Regulatory Affairs Specialist
Central London / West End
Jul 27
Regulatory Professionals are currently working with a long standing and established CRO with global a presence.
Senior Regulatory Affairs Associate
West London
Jul 27
Regulatory Professionals are collaborating with a global bio-pharmaceutical company with a strong pipeline including treatments for cancer, HIV and respiratory diseases.
Associate Regulatory Director
Hertfordshire
Jul 27
This leading research based pharmaceuticals company works across the healthcare sector, aiming to discover and develop innovative medicines worldwide.
Regulatory Affairs Manager - Exciting Global Biopharma, Sussex/South England – upto £70,000 + Bonus + Benefits
West Sussex
Jul 27
We are a growing Global Biopharma going through an exciting period of growth and we are now recruiting for an experienced Regulatory Affairs Manager to champion change, provide full oversight of the regulatory function, work on international projects and lead a team of regulatory professionals. This is a really exciting opportunity offering excellent career development and work-life balance.
Regulatory Affairs Coordinator
Basel area
Jul 26
To coordinate the Project Management and tracking of Regulatory requests received from business partners both internally and externally. In addition, managing the Filing and archiving of Regulatory documents, while supporting regulatory affairs.
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Regulatory Ad Promo Specialists / Experts – Ad Prom incl. Digi and Traditional Media for a high performing franchise
US, East Coast, Relocation offered
Jul 26
This is not your normal type Ad Prom role, as my client has invested heavily in developing and fine tuning a new way of working for our client organization’s Regulatory Ad Prom folks, by bringing critical review to the beginning of the creative process, and repositioning the role, with an emphasis on partnering in the creative process from the start ...
OPTION BELGIQUE Sr / Regulatory Programme Manager EU and GRL Career Pathway No mature products GAIN RA Dev and NEW Lifecycle
Belgium
Jul 26
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!
NEW CONTRACT role for a Regulatory Manager or Sr Reg Manager Do you have Phase I, Phase II CTAs
UK, M4 Corridor
Jul 26
We have a 9 months contract role for a Regulatory Scientist with a dynamic and expanding Biopharmaceutical company based in Berkshire, UK. Good rate is available for the right candidate! You will prepare and deliver regulatory operational plans for assigned projects/products within a specific region, but also provide strategic and operational regulatory input and guidance in cross-functional teams.
Regulatory Affairs Project Manager - Ballaigues, Switzerland or Munich, Germany
Ballaigues, Switzerland or Munich, Germany
Jul 26
Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands.
Regulatory Affairs Technical File Specialist - Ballaigues, Switzerland or Munich, Germany
Ballaigues, Switzerland or Munich, Germany
Jul 26
Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands.
Senior Regulatory Specialist
Central London / West End
Jul 26
Regulatory Professionals are collaborating with a global CRO whom specialise in Clinical trial applications (CTAs).
Senior Regulatory Writer – Part-time - Home Based – UK
Home based, UK
Jul 25
We are a leading Medical Writing consulting looking for a part-time Senior Medical Writer to join our close-knit team and support in producing a wide range of regulatory, safety and clinical documentation for our clients. We pride ourselves in our welcoming culture and dedication to developing all members of our team to expand their skillsets.
Regulatory Affairs Senior Manager - Cambridge
Cambridge
Jul 25
CK Group are recruiting for a Regulatory Affairs Senior Manager to join a company in the Pharmaceutical industry at their site based in Cambridge or...
Regulatory Affairs Manager
Cambridgeshire
Jul 25
Regulatory Professionals are currently collaborating with a top Global Bio pharma company with a truly exciting pipeline,
Regulatory Affairs Senior Manager - 28061
Uxbridge
Jul 25
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Affairs Senior Manager on an initial 6 month contract to be based in their offices in either Middlesex or Cambridge.
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Regulatory Affairs Officer 2 - CMC Specialist
Reading
Jul 25
As a CMC specialist you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a brighter future within Reg Affairs with our selection of development opportunities. At IQVIA, you will get training and development to plan and progress your career in the direction you choose; we do believe there is not a ‘career ceiling. ...
Regulatory Affairs Executive- Hertfordshire, UK
England
Jul 25
My client, a regulatory consultancy, are seeking a Regulatory Affairs Executive to join the medicines team.
Regulatory Affairs Project Manager – Use your Lifecycle exp. to gain better clinical development and CeP experience
Belgium
Jul 25
Working in a strong EU regulatory team, you will also be learning from experienced GRL’s (in the same office), who will help to coach and develop your experience until you are ready to make the leap up to a Global Regulatory Leader. To have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
OPTION SUISSE Regulatory CMC Director Pure mAbs and Team Management role Development and Marketed, US and Europe and Int’l Majors
Switzerland
Jul 25
OPTION SUISSE ** Regulatory CMC Director *** Pure mAbs & Team Management role ** Development & Marketed, US and Europe & Int’l Majors? This role is based in Switzerland, within easy commute of Lausanne, Geneva, or Bern. The role comes with an advantageous package including RSUs.
Director Regulatory Affairs, Biosimilars
Aubonne, Switzerland
Jul 25
Are you passionate about making a difference to patients’ lives? Do you want to build a strong career within a company that excels in delivering high quality research? Why not let our client realise your potential? Join one of the most innovative and exciting companies in the industry! Director Regulatory Affairs, Biosimilars – Global Pharmaceutical Company – Permanent.
Regulatory Affairs Associate
Essex
Jul 24
This emerging pharmaceutical group addressing the clinical needs of patients under specialist care, with an existing focus on gastrointestinal (GI) disease.
Regulatory Senior Executive
Middlesex
Jul 24
SRG are currently looking for Regulatory Senior Executive for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory team to be based at their offices in Middlesex on an initial 12 month contract.
Regulatory CMC Consultant - 12 Month Contract - London
England
Jul 24
I am working with a large consultancy looking to expand their team with an experienced Regulatory CMC Consultant who is to come in and hit the ground running on an initial 12 Month Contract. This is a full-time role based in the London area.
Regulatory Affairs Consultant – Cambridgeshire – 6 months +
England
Jul 24
Regulatory Affairs Consultant, Cambridge, Software Risk Analysis
Regulatory Affairs Senior Manager - Cambridge
Cambridge
Jul 23
CK Group are recruiting for a Regulatory Affairs Senior Manager to join a company in the Pharmaceutical industry at their site based in Cambridge on...
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Senior Regulatory and Start-Up Specialist - Office Based In Neu-Isenburg Or Freiburg
Germany
Jul 23
We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™.
Regulatory Affairs Director, CMC Biologics Geneva Provide Strategic leadership for Global CMC bio projects
Geneva
Jul 23
This role is based in beautiful Geneva, where you will receive a wonderful work life balance for an organisation that is growing and developing its pipeline and also its regulatory team. If you wish to apply for this role or would like to have a confidential discussions, the please call me on my mobile +44 (0)7918 195 166 or direct dial +44 (0)207 801 3384 or email me via Theo@AdvRegulatory.com
Regulatory Affairs Administrator - Poland
Warsaw
Jul 23
At PRA we are recruiting for a Regulatory Affairs Administrator to join our expanding team based in Warsaw.
Senior Regulatory Consultant- Oncology
Cambridge
Jul 20
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a EU Regulatory Affairs Manager- Oncology on an initial 6 Month basis to be based at their offices in Cambridge.The Role:This role will provide regional regulatory support for one or more products. ...
Regulatory Affairs Affiliate Lead UK
Chertsey
Jul 20
I am working exclusively with a reputable pharmaceutical organisation in Surrey that are looking to hire an experienced Regulatory Affairs Affiliate Lead. Need is for an RA Affiliate Lead for a 12 month FTC to start ideally by September /October who will have 2 direct reports and be involved in a number of new launches. There are many new products in pipeline at the moment, lots of extensive prelaunch work.
OPTION SUISSE Regulatory Bio CMC Director Global role on mAbs Are you of a pioneering mind and want to stretch yourself
Switzerland
Jul 20
OPTION SUISSE ** Regulatory CMC Director *** Pure mAbs & Team Management role ** Development & Marketed, US and Europe & Int’l Majors? This role is based in Switzerland, within easy commute of Lausanne, Geneva, or Bern. The role comes with an advantageous package including RSUs.
Senior Regulatory CMC Associate - Specialty Pharma - UK, Home based
UK - Home based
Jul 20
Meet are currently partnering with a specialist Pharma who are looking for a Senior Regulatory CMC Associate to coordinate the preparation of CMC documentation to support regulatory submissions across global territories.
Regulatory Consultant CMC
Macclesfield
Jul 19
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team. They are looking to recruit a Regulatory CMC Consultant on a 12 Month contract basis to their offices in the North West.The Role:My client has a position available for an individual who shares our passion to join the Regulatory Documentation team, Documentation for the CMC part of submissions is one of the key project deliverables from Pharmaceutical Development. ...
Chief of Quality and Regulatory
England
Jul 19
Chief of Quality and Regulatory Affairs Birmingham £ 100,000
Regulatory Information Manager
United Kingdom
Jul 19
5 month contract   Location: UK      TalentSource Life Sciences is currently searching for an experienced Regulatory Information Manager to work with one of our partner pharmaceutical companies in the South of England.       This is a freelance position with TalentSource for 5 months with the possibility of being extended, on a full time basis. This will be an office based position in the Greater London area initially, with potentially some...
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OPTION SUISSE Regulatory CMC Director Pure mAbs and Team Management role Development and Marketed, US and Europe and Int’l Majors
Switzerland
Jul 18
OPTION SUISSE ** Regulatory CMC Director *** Pure mAbs & Team Management role ** Development & Marketed, US and Europe & Int’l Majors? This role is based in Switzerland, within easy commute of Lausanne, Geneva, or Bern. The role comes with an advantageous package including RSUs.
Regulatory Affairs Project Manager – Use your Lifecycle exp. to gain better clinical development and CeP experience
Belgium, Brussels
Jul 18
Working in a strong EU regulatory team, you will also be learning from experienced GRL’s (in the same office), who will help to coach and develop your experience until you are ready to make the leap up to a Global Regulatory Leader. To have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Contract – 12months “Cover CTA’s, PiPs and Scientific Advice prep for EU development Projects”
UK, M4 Corridor
Jul 18
We have a 12 month contract role for an expanding client in the M4 Corridor where you will be preparing scientific and regulatory documents for submission, providing input into development plans and creating regulatory strategy proposals. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com and call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
QA Systems Officer Contract Have you supported CAPAs for PhV and Regulatory Systems 6 months ROLLING
Belgium, Brussels
Jul 18
We have a 16 week contract role for a Global Regulatory Compliance Officer with an expanding Pharmaceutical company based in Brussels, Belgium. If you wish to apply for this role, please send your CV with a covering note to oli.dimitrov@advregulatory.com or alternatively, call Oli in the London office on +44 (0)20 7801 3388.
Senior Drug Regulatory Affairs Manager
Basel
Jul 18
Our client, a dynamic bio-pharmaceutical company, is looking for a Senior Drug Regulatory Affairs Manager for a permanent role based in the Basel area, Switzerland. The ideal candidate should have at least 3 years of experience as Regulatory Affairs Manager, being responsible for the Clinical Trial Applications (CTAs) to regulatory authorities worldwide including submission and maintenance.
Regulatory Submission Manager 12117-1
Kent
Jul 18
Our client a Global Pharmaceutical Company has opened a new vacancy and is looking to recruit a Regulatory Submissions Manager on an initial 12 Month contract to be based at their offices in Kent.
OPTION SUISSE Regulatory CMC Leader Biologicals Live Work Ski in this great location working for an expanding biotech Relo Offered
Geneva - with Full Relocation
Jul 18
The position comes with full support for moving and relocation, and a high level salary and bonus, as well as the normal Swiss benefits. This role is open to any European or US candidate, who has worked on EU or US submissions for regulatory CMC biologicals as a CMC RA Bio Lead, has submitted at least 1 major MAA or a set of major variations, and now wants to move to a global role
Senior Regulatory Affairs Associate
London
Jul 17
Regulatory Professionals are currently collaborating with a top Global Bio pharma company with a truly exciting pipeline.
Regulatory Affairs Consultant – Cambridgeshire – 6 months +
England
Jul 17
Associated keywords: Medical device, Medical Device, Risk Management, ISO 14971, IEC 80002, IEC 62304, FDA Submission
Principle Regulatory Writer - Home Based – UK - £70,000 + car + bonus
Scotland
Jul 16
We are a leading pharmaceutical company looking for a Principle Medical Writer to join our global team and support in a home-based capacity supporting our oncology business. The ideal candidate would have worked with a broad range of clinical documents and have submissions experience.
regulatory jobs : 100 +
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