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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Regulatory Affairs / Director of Global Regulatory Intelligence / US based
US based
May 4
Please call me, Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (evenings / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com.
Regulatory Affairs Manager fuer Medizinprodukte – Pharmaunternehmen – Muenchen – bis zu 90,000 € plus Benefize
Germany
May 4
Wir suchen einen erfahrenen Regulatory Affairs Manager, der seine Erfahrung im Bereich Kosmetika und Medizinprodukten in einem schnell wachsendem und unkonventionellen Pharmaunternehmen nutzen will. Als Gegenleistung erhalten Sie abwechslungsreiche Aufgaben, freundliche Arbeitsatmosphaere und eine exzellente Vergütung.
Associate Director - Regulatory Affairs - Full Lifecycle Role
England
May 4
My client is a top US Biopharma with an enviable commercial portfolio and a robust pipeline in a number of areas of unmet medical need. They are currently looking to hire a senior level individual within their best established therapeutic teams; this will be a role with a significant remit to involve leading new filings via centralised procedure. ...
Regulatory Affairs Specialist II
Jacksonville
May 4
An exciting opportunity has arisen to work for a global, leading specialist Medical Device organization that focusses on offering the world’s most comprehensive portfolio of Visioncare. The position is a Regulatory Affairs Specialist II role to be based on site in Jacksonville, FloridaThe Regulatory Specialist II is a key documentation expert for the Regulatory department. ...
Regulatory Specialist - Medical Devices
Somerville
May 4
ProClinical are currently supporting one of our Global Medical Device clients who are currently seeking a number Regulatory specialists to join their team on a permanent basis.As a Regulatory Specialist you will provide direct regulatory support to various projects and products, both new and existing. Responsibilities may include: Preparing regulatory registration, notification, and pre-market submission requirements, including the necessary regulatory documents. ...
Senior Regulatory Site Activation Manager - Study Start Up - Europe
Europe
May 4
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
Regulatory Affairs, Senior Specialist
Boston
May 4
This Regulatory Affairs, Senior Specialist job is with one of the most renowned global pharmaceutical, medical device and consumer health organisations located in Boston. The organisation is a top 10 pharma company and employs over 100,000 professionals worldwide. Job Role: The Regulatory Specialist will provide direct regulatory support to various projects and products, both new and existing. ...
Freelance Regulatory Affairs Specialist - Pharmaceuticals
Zeist
May 4
For a freelance project with start-date June , my team and I are now urgently looking for a Regulatory Affairs specialist for one of the world’s most famous consumer health/pharmaceutical organization, to be based in the Utrecht region. The project is for six months to replace someone temporarily.You will report directly to the RA/Quality Director and you will be working closely together with three other RA specialists. ...
Regulatory Affairs CMC Bio focused Role South-East Good rate and flexible working with 3 days from home
South East London
May 4
RA CMC Bio contractor wanted for a Global biotech based in the South-East with options to work from home - If you have 3-10 years RA experience with a focus on CMC biologicals then please contact Theo Moore on 0207 801 3384 or email me at cv@advregulatory.com.
Senior Global Regulatory Affairs Associate
London
May 4
Senior Global Regulatory Affairs AssociateCentral London, UKPay Negotiable (Dependant on experience) The CompanyThe company is a top 5 global pharmaceuticals company that focus on development and marketing of high quality, affordable over the counter medicines that can be purchased without the need of a prescription from a healthcare professional. This business is home to some of the biggest and most well-known consumer care brands in the world. ...
Associate, Clinical Trial Regulatory Services (Portuguese speaking)
Madrid
May 4
PAREXEL Spain is looking for Portuguese speaking regulatory professional.
Medical Writer/Regulatory Documentation Scientist x 5 - South East UK
South East
May 4
Medical Writer/Regulatory Documentation Scientist x 5 - UK - South East
Regulatory Affairs Labelling Consultant- US
American Canyon
May 4
Regulatory Affairs Labelling Consultant– 3-6 Months Contract, Home based/Remote US Level: Regulatory Affairs Labelling Consultant Contract: 3-6 Month Contract Salary: Negotiable Location: Home based/Remote UUS Summary We are looking for a Regulatory Affairs labelling to consultant to manage labelling activities for the US. The successful candidate should have a strong grasp of labelling requirements for relevant regulatory authority. ...
Regulatory Affairs Labelling Consultant
England
May 4
Regulatory Affairs Labelling Consultant– 3-6 Months Contract, Home based/Remote UK Level: Regulatory Affairs Labelling Consultant Contract: 3-6 Month Contract Salary: Negotiable Location: Home based/Remote UK Summary We are looking for a Regulatory Affairs labelling to consultant to manage labelling activities for the EU. The successful candidate should have a strong grasp of labelling requirements for relevant regulatory authority. ...
Regulatory Affairs Manager - 6 month contract - Oxford / Bucks
Oxfordshire
May 3
My client, a growing Pharmaceutical company based along the M40 corridor, is currently recruiting for a Regulatory Manager to join their team on an initial 6 month contract basis. This role has become available due to a period of growth within the company and there is a strong chance that this contract will extend beyond the initial period.The ideal candidate will have a full lifecycle background; development (CTA, IMPDs, Clinical Regulatory Updates etc.
Regulatory Affairs Manager, Drug-Device Combination Products
West London
May 3
Pioneering Regulatory Affairs Manager job opportunity to shape the regulatory landscape for Drug-Device Combination products. Working for this well-respected Global Biopharma you will have responsibility ...
UK and Ireland Regulatory Affairs Manager
London-based
May 3
Excellent Opportunity for a UK & Ireland Regulatory Affairs Manager - London-based
Senior Regulatory Officer, Post Approval, Herts
Hatfield
May 3
Senior Regulatory Affairs Officer I am working with a pharmaceutical manufacturer in the search for a Senior Regulatory Affairs Officer, to be based in the...
Associate Regulatory Manager - Biocides
West Sussex
May 3
Regulatory Strategy and Registrations Expert - FMCG Regulations (Biocides & Pesticide)Working with a global FMCG company offering some of the most well known and leading consumer brands, this is an opportunity utilise your packaging experience and data management skills. In a cross category product position, you will play a central role in registrations within EU and partly responsible for global regulations.
Senior Regulatory Affairs Manager – consulting company – Basel - 50 % home and 50 % office based – salary up to 120,000 CHF
Switzerland
May 3
We are currently seeking for an experienced regulatory affairs manager for our Swiss office and be responsible for allocated global projects within regulatory affairs. This position can be full time or part time (4 days) and will be performed 50% of time from home if desired.
Regulatory Consultant CMC
Surrey
May 3
This position will be responsibile for understanding and capturing regional regulatory requirements, developing submission strategy in partnership with GCMC Product strategists and managing lifecycle submissions with the organisations assigned markets. Job Role:•Partners with CMC Strategists and communicates sound regional regulatory requirements and submission strategies for markets in Europe and Emerging Markets Europe (EME) region. ...
Regulatory Affairs und Pharmacovigilance Manager – globales Medizinuternehmen – Wien – bis zu 70,000 € plus Benefize
Austria
May 3
Wir suchen einen erfahrenen Regulatory Affairs/PV Manager, der sich leidenschaftlich fuer Patiensicherung sorgt und gerne in einem professionellen Team die regulatorische und pharmakovigilanze Aktivitaeten uebernimmt. Als Gegenleistung erhalten Sie ein herausfordernde Aufgaben, freundliche Arbeitsatmosphaere und eine exzellente Vergütung.
CMC Regulatory Project Manager
London
May 3
My client provides expert advice to the biopharmaceutical industry on process/product development and strategic regulatory affairs. With a proven track record of success, we have worked on more than 400 medicinal products in its 26-year history. This places us in an unrivalled position as consultants in this demanding and highly specialised arena.Our team specialises in biological medicinal products, including monoclonal antibodies, biosimilars, and advanced therapy medicinal products. ...
Regulatory Specialist
York
May 3
Regulatory Affairs / Regulatory Specialist / Senior RA SpecialistLocation: York / Birmingham / homebased  An excellent opportunity for an experienced Regulatory Specialist has become available to join a rapidly growing Medical Device Company on a permanent basis. This organisation have a site based in Birmingham Central and also York, North Yorkshire and they would be open to an element of homebased working. ...
Regulatory Affairs Manager (m/w) NEMs/Kosmetika
Frankfurt am Main
May 3
Regulatory Affairs Manager (m/w)Office-based in FrankfurtJob Description:- Management of international regulatory processes pertaining to non-pharmaceutical products, particularly feed supplements and cosmetics for medicinal use.- Consulting the internal sales and commercial teams regarding the marketability of the products. ...
Regulatory Affairs International Product Lead - Strategy
Berkshire
May 3
You will be accountable for defining the International regulatory strategy for your assigned products. You will also collaborate closely with all other key GRA stakeholders which includes advertising and promotion, labeling, CMC, regulatory operations, EU regulatory team and regulatory staff in the International locations to ensure that all aspects of the regional strategy is coordinated and considered.
Regulatory Consultant
Surrey
May 3
This Regulatory Consultant job is an excellent opportunity to work for a global leader in biopharmaceuticals located in Surrey, South East England. The company has been established for more than 150 years and is a major supplier to the NHS.This is a 6-month contract with the possibility of an extension. Job Role: This Regulatory Consultant job role will include allowing the company to legally study, manufacture, market and supply medicines. ...
Regulatory Labelling Coordinator
Surrey
May 3
This Regulatory Labelling Coordinator job is an excellent opportunity to work for a global leader in biopharmaceuticals located in South East England. The company has been established for more than 150 years and is a major supplier to the NHS.This is a 12-month contract with the possibility of an extension. ...
Regulatory Consultant CMC
London
May 3
This job is a great opportunity for a Regulatory Consultant CMC to work at one of the top 10 global pharmaceutical companies. This role will be based at the company’s Hertfordshire office. The organisation develops innovative products across multiple therapy areas including cardiovascular, oncology, and respiratory, and employs 100,000 staff globally. This is a 6-month contract with the possibility of an extension. ...
Regulatory Affairs Manager for CMC Biologicals 12 month Lucrative CONTRACT
Brussels
May 3
Develop effective proactive CMC strategies for new products and for lifecycle regimes in International and Emerging Markets and acts as the lead CMC expert for review and finalising regulatory strategy documents and building submissions. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
IMPROVE YOUR SKILLS: Pharmacist Regulatory Affairs
Picardie
May 3
Do you feel bored at work? Do not miss this unique opportunity! My client is looking for a Junior Pharmacist within the field of Regulatory Affairs to work on a variety of product such as cosmetic, medical devices, food supplements. This is the perfect opportunity to improve your skills and get a better CV for your future.
Regulatory Affairs Senior Manager – CMC Biologics / Vaccines / Mabs – Full project lifecycle role with Global project responsibilities – South-East
Berkshire
May 3
You will have the opportunity to work on a complete range of regulatory applications, indications and molecules. This is varied position covering early, mid, late stage and centralised filing.If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Labeling Consultant
New York
May 3
This is a great opportunity for a Regulatory Labeling Consultant to join a well-established organisation based in New York USA. This is a 12-month contract with the possibility of an extension. Job Role: - Manages the development, review, approval, and maintenance of the Company Core Data Sheets (CCDS), USPI, and EU SmPC. - Maintains and appropriately archives submitted and approved labeling documents and packaging component labeling. ...
Regulatory Affairs Snr Manager for CMC CMC Biologicals Contract Based in Berkshire – Excellent rate
England
May 3
Regulatory CMC leader for European and International regulatory submissions, requirements and procedures, pre & post-licence If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs CMC Role for a Global Biotech – Expansive role with great training
South-East
May 3
There is still flexibility for the project(s) that you will be working on but it will be matched between your experience, your strengths and your ideal role. So in essence you could be supporting a project in late phase to MAA and/or be working on some market expansion activities. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs CMC Bio Snr Manager and Associate Director roles for a global biotech company – From PI to PIII and registration - Brussels
Brussels
May 3
This organisation has a fantastic portfolio of products in development so you will have a great platform from which to take the lead in your projects - This organisation has a fantastic portfolio of products in development so you will have a great platform from which to take the lead in your projects
Regulatory Affairs Snr Manager EU Lifecycle Management role for Exciting Product Portfolio New indications, major extensions
The Netherlands
May 3
By joining this amazing organisation you will follow a large numbers of employees who have built unique and rewarding careers as the company has grown. With continued growth on the horizon, there's no end in sight to your career possibilities! Contact Theo Moore or Matt Greig on +44 (0) 207 801 3384
Regulatory Affairs EU Project Manager - Strategic role where your lead strategy and submissions for EU and RoW
Central Netherlands
May 3
This will be a results orientated strategic leadership role where your strategy and regulatory knowledge will carve a path for product submissions and registrations ion the EU and other major RoW/International territories. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Associate Director – Full project lifecycle role covering EU Development and MAA’s for an expanding Bio/Pharma
The Netherlands
May 3
This is an excellent role for those that seek autonomy and want to work with an organisation that has a good pipeline and is now ready to grow - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs CMC Contract Roles for an International Pharmaceutical company based in South-East / Greater London
Souoth-East
May 3
We have 2 new Regulatory Affairs CMC Contract Roles for an International Pharmaceutical company based in the South-East who have a pipeline of both Pharmaceutical and Biological products. Both roles are leadership roles where you will be providing strategic CMC guidance for your projects.
Senior Associate, Regulatory Affairs International - France
Paris, France
May 3
I am currently partnering with an exciting, fast paced, high-growth ascendant pharmaceutical business that offer an incredibly diverse portfolio, achieved through a number of very successful strategic acquisitions. With an impressive Dermatology portfolio, the company are looking to expand their Regulatory capability through the appointment of a new Senior Associate to cover the international region.
Regulatory Biologics (all levels)
London
May 3
Regulatory Affairs Biologics Candidates (All levels may apply)Consultancy considering candidates with Biologics experience (all levels) CompanyI am currently sourcing for candidates with strong Regulatory Affairs Biologic experience to join a large growing consultancy. They are looking to expand their team within this area and are open to seeing different levels of candidates from Regulatory Affairs Associate through to a Senior level. ...
Senior Regulatory Associate
Hertfordshire
May 3
Senior Regulatory Officer – London / HertsAn exciting opportunity has arisen to join this global company and manage their Regulatory activities. You will be involved in the entire life-cycle of products. ...
Senior Regulatory Writer – Switzerland
Zürich
May 3
IM/130268/10Head of Regulatory Writing - SwitzerlandI am currently looking for an experienced regulatory writer, preferably from a CRO background, to join an exciting and dynamic agency in a new position.This position is the perfect opportunity for an experienced regulatory writer, who experience either in an agency or CRO setting, and aspires to develop their leadership skills within an international environment working with an excellent team and reputation.
Regulatory Affairs Manager-Immediate Interviews-Midlands
Birmingham
May 3
Regulatory Affairs Manager-Immediate Interviews-MidlandsAre you able to offer experience with a range of products from Pharmaceutical's, OTC and Medical Devices? If so then my client has the perfect opportunity for you! As the Regulatory Affairs Manager you will join a small team who are rapidly expanding across the EU.
Regulatory affairs- Prague-Growing service provider
Prague
May 2
If you are looking for new challenges and to broaden your experience in regulatory then this is a perfect opportunity for you. You will be working with latest projects and a wide scope of clients to broaden your experience.
Regulatory affairs- Märkning-Sverige
Sweden
May 2
Jag är specialist head-hunter inom Regulatory Affairs på svenska marknaden, med speciell fokus på Läkemedels- och biofarma branschen. Just nu jobbar jag med flera etablerade och globala kunder som just nu expanderar och söker nya medarbetare med erfarenhet inom regulatorisk märkning.
Regulatory Affairs Manager (m/w) Submissions
Frankfurt am Main
May 2
Regulatory Affairs Manager (m/w) SubmissionsOffice-based / Home-based im Raum FrankfurtAufgaben:- Erarbeitung von Zulassungsstrategien für globale Einreichungen- Logistische Vorbereitung und Koordinierung von Zulassungsverfahren in Zusammenarbeit mit Niederlassungen und Kooperationspartnern- Erstellung der administrativen Unterlagen von Zulassungsdossiers (Modul 1) aus MR-, DC- und nationale Verfahren- Kompilierung kompletter Zulassungsdossiers für globale Einreichungen- Life-Cycle Managemen ...
Regulatory Operations Manager (m/w)
Frankfurt am Main
May 2
Regulatory Operations Manager (m/w)Office-based near Frankfurt, GermanyJob Description:- Participate in the daily activities and workload of site publishing team, ensuring compliance with all SOPs and internal publishing standards- Contribute to major and complex routine/lifecycle management eCTD submission projects- Maintenance and continuous improvement of publishing tools and standards- Participate in Global Regulatory Operations management meetings- Participate in Global Regulatory Affai ...
EXTEND YOUR NETWORK: Pharmacist Regulatory Affairs
Picardie
May 2
Do not miss this unique opportunity! My client is looking for a Junior Pharmacist within the field of Regulatory Affairs to grow with them. It offers you to start your career working with a variety of products which will provide you a unique set of skills.
Senior Regulatory Affairs EU und DE Zulassungsprojekte
Stuttgart
May 2
Zur Zeit Suchen wir in Stuttgart eine/n Regulatory Affairs Manager/in: Ein Familienunternehmen in Stuttgart sucht fuer das internationale Headquarters team einen Regulatory Affairs Manager fuer EU und Deutsche Zulassungsprojekte. Das team ist sehr kollegial und professionell und bietet vielseitige Aufgaben und gute Weiterentwicklungs-moeglichkeiten an. ...
REGULATORY AFFAIRS-CONSULTING GLOBAL PHARMA COMPANIES-GERMANY
Germany
May 2
My client is a well known pharmaceutical consulting company in Germany, with extensive experience in Regulatory Affairs, looking for two new Regulatory Affairs Managers to join the consultancy office. ...
Scientific Development Regulatory Affairs Herbal
Leverkusen
May 1
Wir suchen zur Zeit in Leverkusen eine/n Scientific Manager/in Regulatory Affairs: Aufgaben * Verantwortlich für die medizinisch wissenschaftliche Betreuung von Produktneu- oder Weiterentwicklungen von Arzneimitteln * Wissenschaftliche und regulatorische Planung von Entwicklungsprojekten für Arzneimittel * Erstellung von vorklinischen und klinischen Entwicklungsplänen auf Basis der relevanten regulatorischen und klinischen Guidelines * Planung und Kontrolle von pharmakologisch-toxikologisch ...
Regulatory PM - start-up company - NRW
Dusseldorf
May 1
A position with what is essentially a start-up company, resulted from the spin-off from a global giant, has just opened up in Duesseldorf Germany. They offer a promising pipeline to work with as well as the stability that comes from the large investments and partnerships they have already managed to attract. If you wish to be a part what may be the humble beginnings of a new global giant then don't hesitate to apply today. ...
CMC Documentation Manager Regulatory Affairs Austria
Salzburg
May 1
A mid-sized pharma company headquartered in Austria is expanding their already successful regulatory affairs team and add on board a Documentation manager for CMC. The manager is looking for someone who wants to progress quickly in a competitive environment and who can eventually develop to lead a team. ...
Senior Regulatory Medical Writer
Zurich area
Apr 29
Edelway is a pan-european Pharma Consultancy. One of our best clients, a global, pharmaceutical company based in Zurich Area is currently looking for experienced Senior Regulatory Medical Writer.
Regulatory Spezialist-Chemicals-Nord Deutschland
Germany
Apr 29
Regulatory Specialist-Chemicals-Nord DeutschlandBei einem unseren weltbekannten Kunden in Nord Deutschland, einem Unternehmen in der Chemiebranche, bietet sich diese interessante Perspektive im Rahmen einer Festanstellung.
Regulatory Affairs Manager-Well Established Product Range
Birmingham
Apr 29
Regulatory Affairs Manager-Large Product Portfolio-MidlandsI am working with a healthcare company in the Midlands who are currently looking to expand their team with a Regulatory Affairs Manager. Due to their expansive and already established portfolio they are looking for somebody who can offer experience with a wide range of products and in return you will be given the chance to take a lead on all regulatory activities.
Regulatory Affairs-Project management-Prague
Prague
Apr 29
For my client I am looking for regulatory affairs professionals to further develop their regulatory services to their clients! They are strongly expanding and hence looking for someone to develop together with them and their wide span of clients which will be beneficial for your career development in regulatory, since you will be working with highly talented colleagues and interesting projects.
Regulatory affairs-CMC-Sverige
Sweden
Apr 29
Jag är specialist head-hunter inom Regulatory Affairs på den svenska marknaden, med speciell fokus på Läkemedels- och biofarma branschen. Just nu söker flera av mina klienter efter registrerings-verksamma med CMC erfarenhet.
Regulatory Affairs Associate
Dublin
Apr 29
Our client is an expanding consultancy firm specialising in European and U.S. regulatory affairs and quality assurance. A vacancy currently exists for a Regulatory Affairs Associate.
Senior Regulatory Affairs Specialist
Wiltshire
Apr 29
I am searching for an experienced individual to join a Global Medical Device company in the Wiltshire area as a Senior RA Specialist.
Regulatory Specialist
Worchestershire
Apr 29
I am currently searching for an RA Specialist to work in a Global Medical Device company based in the Worcestershire area.
Career in Regulatory Affairs Pharmacist
Picardie
Apr 29
Do you want to start your career as a Regulatory Affairs Pharmacist? My client is a growing company which you can progress and evolve with. This innovative company has created the first network of independent pharmacies and needs you to manage the regulatory affairs for a variety of products.
SENIOR DIRECTOR, REGULATORY and SITE SERVICES, EUROPE
Anywhere Europe
Apr 29
The successful individual will play a vital strategic role in developing this new department.
REGULATORY AFFAIRS-GERMANY-SUCCESSFULL CONSULTANCY
Germany
Apr 29
Are you a flexible regulatory affairs professional, looking for a new opportunity that gives you the flexibility and variety of a contract position with the long term benefits of a permanent role?My client is a successful pharmaceutical consulting company in Germany, with extensive experience in Regulatory Affairs, looking for two new Regulatory Affairs Managers to join their consultancy office. ...
Regulatory Affairs Director – ATMP – Belgium
Antwerp
Apr 29
A biopharmaceutical company is looking for a regulatory affairs director who will execute worldwide clinical submissions for an advanced therapy portfolio. The company is specialized in antibodies to put innovative medicines on the market that treat under targeted diseases. In that way you are at the forefront of innovation what makes your role even more interesting.
Regulatory Affairs Manager-Large Product Portfolio-Midlands
Birmingham
Apr 28
Regulatory Affairs Manager-Large Product Portfolio-MidlandsI am working with a healthcare company in the Midlands who are currently looking to expand their team with a Regulatory Affairs Manager. Due to their expansive and already established portfolio they are looking for somebody who can offer experience with a wide range of products and in return you will be given the chance to take a lead on all regulatory activities.
Regulatory Affairs Manager – UK affiliate role – Project lead
Cambridge
Apr 28
This is an opportunity to join a midsize pharma and lead their UK/ IRE post marketing activities. With the preparation of MAAs & CTAs; liaison with LOCs; and wider scientific guidance given to global regulatory teams, this is an expansive role. On a 2 year contract, this post will give a level of experience to the post holder which allows them to find a more senior level role on completion.
Regulatory Affairs Director, Biotech, London
London
Apr 28
Regulatory Affairs Director – Niche Biotech – Central London A niche biotech based in Central London are searching for a Director of Regulatory Affairs to...
Senior Manager of Regulatory Affairs - EMA Liaison – UK
London
Apr 28
Leading the life cycle management for a major large molecule product in the EU, this contract offers the successful applicant a strategic post with agency liaison responsibilities. The role will require a regulatory professional with 6 -8 years of experience where they have been the point of contact for the EMA or CHMP.
Regulatory affairs- Prague
Prague
Apr 28
I am currently working with a client who is a service provider for the life science industry and they are currently expanding their regulatory team due to achieve their vision of becoming the ultimate global service provider. This will give you an amazing opportunity to widen your experience and grow within a quality-minded company.
Regulatory Submission Coordinator– global CRO/Contract research organization Munich – 60,000 €
Germany
Apr 28
We are currently seeking for an energetic and motivated Regulatory Submission Coordinator to join our clinical team and manage clinical trial application submissions in the DACH region on a permanent basis for a salary up to 60,000 €
Regulatory Affairs Manager - Central London
London
Apr 28
An excellent opportunity has arisen for a Regulatory Affairs Manager to join an industry leading organisation based in central London on a permanent basis. This role will suit an individual with a strong scientific or clinical regulatory background, and will offer excellent career progression working within an oncology focussed team.
REGULATORY AFFAIRSSUCCESSFULL CONSULTANCY-GERMANY
North Rhine-Westphalia
Apr 28
Are you a flexible regulatory affairs professional, looking for a new opportunity that gives you the flexibility and variety of a contract position with the long term benefits of a permanent role?My client is a successful pharmaceutical consulting company in Germany, with extensive experience in Regulatory Affairs, looking for two new Regulatory Affairs Managers to join their consultancy office. ...
Senior Regulatory Affairs Associate, EMEA
England
Apr 28
inVentiv Health -Transforming Promising Ideas into Commercial Reality12694 Senior Regulatory Affairs Associate, EMEAAs a key member of our global regulatory team you will assigned to specific project teams where your main responsibility will be to coordinate the regulatory and ethics submissions for the study. As Senior Regulatory Affairs Associate you may be assigned to multiple projects depending on size and complexity, primarily for phase II and III studies. ...
Regulatory Affairs Project Manager
Elstree
Apr 28
An exciting opportunity for a Regulatory Affairs Project professional has arisen to join Bio Products Laboratory (BPL), a niche pharmaceutical business based near to Watford, at a time where it is embarking on a programme of investment in all parts of the business.
REGULATORY SPECIALIST- SOUTH GERMANY
Germany
Apr 28
My client, leading producer of stored product protectants, is currently looking for a Regulatory Specialist, to join its Regulatory Department in South Germany.
Urgent SSU and Regulatory Affairs Specialist
Slovakia
Apr 28
SSU & Regulatory Specialist – Slovakia – Immediate start - HOME BASED Level: Study Start Up & Regulatory Specialist Contract: 12 month contract home based Salary: Negiotiable Location: Slovakia Summary We are looking for a SSU & Regulatory Specialist to join a renowned pharmaceutical company. As a member of our Study Start Up team you will be involved in all therapeutic areas and phases, providing your expertise at this vital period of time in the study. ...
Regulatory Manager Roles, London/Cambridge
Cambridge
Apr 28
Regulatory Affairs Roles in Clinical, Post Approval and Biologics DevelopmentTogether with a specialist pharmaceutical services provider, Skills Alliance is searching for Regulatory Affairs Managers...
Regulatory Affairs Medical Writer – Remote Working – 12 MONTH CONTRACT
USA
Apr 27
We are currently seeking a Freelance Regulatory Affairs Medical Writer to join our award winning global company on a 12 month contract and enjoy the luxury of remote working, The Regulatory Affairs Medical Writer will be involved in clinical global projects while receiving a lucrative hourly rate
Regulatory Affairs - Toksykologia- UK
England
Apr 27
Regulatory Affairs - Toksykologia- UKNiepowtarzalna okazja dla wyksztalconego toksykologa, który szuka nowych wyzwan i jest zainteresowany praca dla jednego z najwiekszych koncernów na swiecie.Pracujac dla mojego klienta, nie tylko zglebisz swoja wiedze w zakresie Regulatory Affairs, ale równiez poszerzysz swe horyzonty i rozwiniesz wlasna siec kontaktów. ...
Regulatory Affairs Associate - Cardio/Respiratory Devices
Munich
Apr 27
Are you a Regulatory Affairs Professional looking the the Medical Devices field? Looking for a new opportunity? Click here...
Regulatory Affairs Manager.dynamic company.Veneto
Veneto
Apr 27
Se stai cercando l'opportunita' che dara' la svolta alla tua carriera, questa e' l'occasione che fa per te! Il mio cliente, una azienda dinamica nel field medical devices, sta cercando un Regulatory Affairs Manager con esperienza con le norme ISO 9001, 13485, 13485 CMDCAS e 21 CFR 820.
Head of Regulatory Affairs - Medical Devices - International team -Belgium
Belgium
Apr 27
To apply for this Head of Medical Devices - Regulatory role please call Julie Cooper on 07951 082482 Or email your Cv to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Executive - North London
England
Apr 27
Regulatory Affairs Executive - North London Medical Devices. Our client is a medical devices company operating in over 40 countries manufacturing and distributing its product portfolio ranging from personal care to surgical devices.
Senior Regulatory Affairs Specialist - Medical Devices
England
Apr 27
Senior Regulatory Affairs Specialist - Medical Devices North West. Our client is a leading multi-national medical device manufacturer based in North West. They are presently looking to recruit a Senior RA Specialist with EU medical device experience.
Regulatory Officer
North
Apr 27
A growing Nutrional company is looking for a Regulatory Officer to work on post marketing activities. You would be working in a close knit team of 5 people, reporting to the Head of Regulatory learning from someone who has over 20 years experience.
Regulatory Affairs Associate
England
Apr 27
Working as part of the Genpact Pharmalink Consulting team gives you a career that will be varied, diverse and never dull! You will be joining a team of the best Regulatory Affairs Professionals in the industry, some of the most experienced and progressive minds. Our consultants come from a wide spectrum within the Healthcare Industry, all bringing invaluable skills and attributes that allow us to provide the best Regulatory Affairs expertise to our clients.
Regulatory Specialist-Chemicals-UK
England
Apr 27
A recent opportunity has come up for an experienced REACH Specialist, who wants to be a part of one of the leading companies within the consumer products sector.
Regulatory Affairs-Pharma-Prague
Prague
Apr 27
For my client I am looking for regulatory affairs professionals to further develop their regulatory services to their clients! They are strongly expanding and hence looking for someone to develop together with them and their wide span of clients which will be beneficial for your career development in regulatory, since you will be working with highly talented colleagues and interesting projects.
Regulatory Affairs Manager – Promotional Material
Brussels
Apr 27
A global pharmaceutical company is looking for a Regulatory Affairs Manager to be the link between the international and Benelux team. You will be also responsible for life cycle management and the approval of promotional material. In that way you are also involved in the creative part and feel more responsible.
Regulatory Affairs Specialist - ROW role - Cambridge - UK
Cambridge
Apr 27
To apply for this regulatory affairs specialist role please call Julie Cooper on 07951 082482 or email on:julie@mosaicrecruitment.co.uk
Regulatory Affairs Specialist - ROW
Cambridge
Apr 27
To apply for this role please call Julie Cooper on 07951 082482 or email Julie Cooper @julie@mosaicrecruitment.co.uk
Regulatory Affairs Associate Manager - Operations- Cambridge
Cambridge
Apr 27
To apply for this associate regulatory affairs operations manager please call Julie Cooper on 07951 082482 Alternatively please send your CV to : julie@mosaicrecruitment.co.uk
Regulatory Affairs Project Manager - consultancy work - Surrey
Surrey
Apr 27
To apply for this regulatory affairs project manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to- julie@mosaicrecruitment.co.uk
Consulting Manager - Regulatory Affairs - Surrey -UK
Surrey
Apr 27
To apply for this regulatory affairs consulting manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Specialist Cosmetics - Midlands- International role- Exciting new role
Nottingham
Apr 27
To apply for this regulatory affairs cosmetics role please send your CV to;julie@mosaicrecruitment.co.uk or to discuss further please give Julie cooper a call on 07951 082482
Regulatory Affairs Manager - Cosmetics - Nottingham
Midlands
Apr 27
To apply for this regulatory affairs cosmetics role please call Julie Cooper on 07951 082482 Alternatively please send CV to :julie@mosaicrecruitment.co.uk
SSU and Regulatory Specialist II - Study Start Up - Italy
Saronno
Apr 27
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
jobs : 100 +
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