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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Regulatory Affairs Consultant- Spain
Spain
May 27
Regulatory Affairs Consultant- 6 Month Contract- Spain, EU Level: Regulatory Affairs Consultant Contract: 6 months Salary: Negotiable Location: Spain, EU Summary Regulatory Affairs Consultant is required to manage local regulatory submissions for Spain. The successful candidate will be responsible for post approval activities such as maintaining the MAA by ensuring that variation, licences renewals and label changes are updated on a timely manner. ...
Senior Regulatory Associate, Study Start Up (Homebased)
Home Based
May 27
Rare Senior Regulatory Affairs job opportunity to join a growing, privately owned Oncology/Onco-Haematology specialist CRO as the first regulatory affairs appointment, at the start of...
Regulatory Affairs Consultant
London
May 27
Excellent opportunity for a Regulatory Affairs Consultant to join a well established pharmaceutical company based near London. Key requirements for this position: - Strong experience with...
Regulatory Consultant (Fully Home-Based)
England
May 26
i-Pharm Consulting are recruiting for…JOB TITLERegulatory Affairs Consultant LOCATION: Fully Home-BasedRATE: Negotiable ROLE: International & growing CRO are looking for a Regulatory Consultant to be home-based within the UK and work primarily on clinical trial application documentation as well as provide advice to pharmaceutical companies on compliance and regulatory issues surrounding Clinical Trial Applications. ...
Regulatory Consultant (Fully Home-Based)
England
May 26
i-Pharm Consulting are recruiting for…JOB TITLE: Regulatory Affairs Consultant LOCATION: Fully Home-BasedRATE: Negotiable ROLE: International & growing CRO are looking for a Regulatory Consultant to be home-based within the UK and work primarily on clinical trial application documentation as well as provide advice to pharmaceutical companies on compliance and regulatory issues surrounding Clinical Trial Applications. ...
Clinical Study Start-Up and Regulatory Specialist – Freelance
Buckinghamshire
May 26
Clinical Study Start-Up & Regulatory Specialist - Freelance i-Pharm Consulting are seeking an experienced SSU & Regulatory Specialist to work on a 12 month contract with a leading Bio-Tech based in the Buckinghamshire region.
Regulatory Affairs Manager Grow in pharma
New York
May 26
NY/Regulatory Affairs Manager/Grow within the Pharma Industry I am working with a international Italian company facing a moment of great growth, both on the market and in terms of pipeline development. You will work with qualified colleagues that will enlarge your knowledge.
Regulatory affairs-Russia-Leading CRO
Russia
May 26
I am currently recruiting for a leading , global service provider providing a wide range of services in dynamic industries as pharma, biotech and medical devices just to mention a few. If you are looking to work internationally with varied and exciting projects to gain wider experience and to grow your international network- then this might be the next step in your career.
BIOZIDE EXPERTEN- Regulatory Affairs
Germany
May 26
BIOZIDE EXPERTEN- Regulatory AffairsBei einem unseren weltbekannten Kunden in Nord Deutschland, einem Unternehmen in der Chemiebranche, bietet sich diese interessante Perspektive im Rahmen einer Festanstellung.
Global Regulatory Specialist - Crop Protection
Surrey
May 26
Global Regulatory Specialist - AgrochemicalWorking for a large multinational within the crop protection business, you will work within weed and seed care helping with regulatory dossier submission. Our client is an established organisation looking to expand further to an already extensive product range.
Director, Regulatory Affairs and Quality Assurance
New Hampshire
May 26
My client is a global leader with a broad portfolio in Devices & Pharmaceuticals.
Regulatory Affairs Project Manager - consultancy work - Surrey
Surrey
May 26
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
May 26
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 Specialist - Agrochemical
Surrey
May 26
Regulatory Officer - Crop Protection . AgrochemicalsWorking for a large multinational within the crop protection business, you will work within weed and seed care helping with regulatory dossier submission. Our client is an established organisation looking to expand further to an already extensive product range.
Regulatory Records Specialist - Camberley
Camberley
May 26
Do you want to be a part of a global top 10 CRO? We are currently looking to strengthen our Document Control team in the UK and are seeking a temporary Regulatory Records Specialist to start in June 2016, for a 6 month period to be based in our Camberley office.
Exp Medical Writer (Regulatory) Home-Based
England
May 26
Exp Medical Writer (Regulatory) Home-BasedThis is a home-based role, which is very rare in pharma and super convenient if that's what you are after! Furthermore this is a varied position with a focus on virtual team leadership and spearheading statistic consulting: not a regular boring job, actually very interesting.
Regulatory affairs/CMC/Denmark
Denmark
May 26
Excellent opportunity in Copenhagen for you with a strong background in CMC!
Senior Registration Officer / Senior Regulatory Officer
Hertfordshire
May 26
Experienced lifecycle regulatory affairs professional required for full-time permanent position in Hertfordshire. Competitive package available with global company.
Regulatory Document Specialist/Study Start Up - Global Pharma - £250+ per day
England
May 26
We are looking for a Clinical Study Specialist for a global pharma in Buckinghamshire. The role is a 12 month contract and will be very focused on Study Start Up- experience in this is essential. The successful candidate will have responsibility for all essential clinical trial documents relating to study start up. This is a great opportunity to join a successful pharma company who are growing consistently and steadily.
Regulatory Writer – Switzerland
Zürich
May 26
IM/130268/11Head of Regulatory Writing - Switzerland I am currently looking for an experienced regulatory writer, preferably from a CRO background, to join an exciting and dynamic agency in a new position.
Regulatory Affairs Manager - Full Product Life-Cycle
Russia
May 26
My client is a globally known CRO, currently looking for a new Regulatory Affairs Manager to join them in Russia and help with regulatory expertise for different international projects. This is an excellent opportunity for candidates to gain international experience and join a quickly progressing company, that will allow them to professionally develop within it. ...
Regulatory Compliance Officer - WEEE and Toy Directive
Norfolk
May 26
Our client is a growing organisation with a newly appointed CEO who, is looking to diversify the company product range into more lucrative markets with higher profit margins from it's product ranges. The organisation product ranges focus on the consumer product and FMCG sector with a electronics and toys making the bulk of its products. This is a chance for somebody with perhaps a regulatory bakground or electronic engineering background to take on a compliance function.
Regulatory EcoToxicologist – Family Atmosphere - France
Lyon
May 26
This is an exciting opportunity for an experience professional to work with some of the biggest names in the Agrochemical industry where you will be supporting companies in the registrations process of plant protection products through drafting of submission documentation and conducting risk assessments offering a very challenging and dynamic working environment.
Regulatory Associate - CTA
Middlesex
May 26
Regulatory Associate - CTAA fantastic opportunity for a Regulatory Professional to join a global CRO. An experienced Regulatory Associate with a background in clinical research with a passion for drug development.Must be eligible to work in the UK. ...
SSU and Regulatory Specialist - Buckinghamshire - 12M Contract
Buckinghamshire
May 26
Study Start Up and Regulatory Specialist - Buckinghamshire - 12 Month Contracti-Pharm Consulting are seeking on behalf of a Leading Pharmaceutical company a Study Start Up Specialist who's interested in furthering their career into the Pharmaceutical Industry.
Head of Regulatory Affairs - Medical Devices - International team -Belgium
Belgium
May 26
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
Associate/Director/Senior Director, Regulatory Affairs - EMEA-129290
Europe, Middle East and Africa-UK-England-Cambridge - Granta Park 1
May 26
PPD has a new opportunity for an Associate Director/Director/Senior Director to join our Regulatory Affairs Team, based in Europe to lead our regulatory Functional Services Solutions team.  This is a challenging and exciting opportunity in which you can take your career to the next level.   The purpose of this role is to lead our regulatory Functional Services Solutions team.  This is a challenging and exciting opportunity in which you can take your career to the next level. ...
Regulatory Affairs Manager Learn and grow
New York
May 25
NY/Regulatory Affairs Manager/Learn and grow. I am working with a international Italian company facing a moment of great growth, both on the market and in terms of pipeline development. You will work with qualified colleagues that will enlarge your knowledge.
Regulatory Affairs Specialist
Switzerland
May 25
A world class, innovative Pharmaceutical Company with a superb pipeline of products are searching for a Regulatory Affairs Specialist. Your main role will be to manage the product clinical trial applications to applicable Health Authorities within the EU.
Senior Regulatory Associate - Medical Devices
Kingston Upon Hull
May 25
My client is a reputable global company in the healthcare sector and they are seeking a Global Regulatory Affairs Senior Associate to assist in making sure regulatory and compliance standards are kept up to the relevant regulations and standards.This position has the prospect of leading a working at the forefront of the industry; creating a varied, interesting working environment and ultimately, exposing you to the global healthcare sector. ...
Drug Regulatory Affairs Manager -
Switzerland
May 25
I am currently looking for a Drug Regulatory Affairs Manager to work with one of the world’s leading manufacturer of Natural cosmetics and anthroposophic medicines based in Basel, Switzerland
Regulatory Submission Coordinator– global CRO/Contract research organization Munich – 55,000 €
Germany
May 25
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 55,000 €.
Regulatory Affairs und Pharmacovigilance Manager – globales Medizinuternehmen – Wien – bis zu 70,000 € plus Benefize
Austria
May 25
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.
Senior Regulatory Scientist
Surrey UK
May 25
I am currently holding an exciting position working for a growing CRO. You would be participating as a team member, project manager, or advisor for a certain number of their international projects, working in an international environments.
Regulatory Manager
North England
May 25
I am working with a growing generics company based in the North of the UK. To go alongside their growth they are looking for a Regulatory Manager to look over already marketed products.
Head of Regulatory Affairs - Medical Devices - International team -Belgium
Belgium
May 25
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
Senior Start-up and Regulatory Specialist - Basel
Basel
May 25
Manage and perform tasks at country level in accordance with applicable local and/or international regulations, standard operating and contractual/budgetary guidelines, including pre-award activities,  oversight the scope of work, budget and ressources. RESPONSIBILITIES Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Management and CST. ...
Regulatory Submissions Manager
London
May 25
Regulatory Submissions ManagerLooking to gain more experience in Regulatory Affairs? A mid-sized CRO based in London are looking for a Regulatory Submissions Manager to joining the Clinical Operations Team. Candidates with a background in global start-up are encouraged to apply. Candidates must be eligible to work in the UK. ...
Director, Quality Assurance and Regulatory Compliance, Europe
England
May 25
inVentiv Health Clinical is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 6,500 passionate employees supporting clients in more than 70 countries, inVentiv Health Clinical works to accelerate high quality drug development programs of all sizes around the world.
Regulatory Affairs Consultant- Netherlands
Netherlands
May 25
Regulatory Affairs Consultant- 3-6 Month contract- Immediate Start- Netherlands Level: Regulatory Affairs Consultant Contract: 3-6 Months Location: Netherlands, EU Salary: Negotiable Summary We are looking for a Regulatory Affairs officer to join a renowned pharmaceutical company. The successful candidate will complete local submissions of marketing authorization applications for a diverse pharmaceutical portfolio. ...
Senior Regulatory Affairs Manager
Harlow
May 25
Are you keen to join a leading regulatory affairs team? Do you have management experience? We're looking for someone like you… Teva currently have an excellent opportunity for a Senior Regulatory Affairs Manager to join the OTC Regulatory team, mainly focusing on new submissions on a global scale. You will have line management responsibilities in this position, contributing to the success of the OTC team.
Regulatory Affairs Specialist
England
May 25
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Head of Regulatory Affairs
Madrid
May 25
Barrington James have been exclusively retained to search and select a Head of Regulatory Affairs on behalf of a specialist Biologics organisation that will offer the successful candidate an unparalleled opportunity to become part of a company who have achieved 25% year on year growth. This is a permanent position that will be based out of the company's HQ in the heart of Madrid.
Associate Director Regulatory Affairs
Rep. Ireland
May 25
Are you looking to work with Autonomy? Do you want to join a rapidly growing EU Regulatory Function?
Senior Regulatory Affairs Associate
Berkshire
May 24
The company is a leading full service CRO which advises clinical and product development strategies to achieve commercial targets and business growth. They use a unique blend of scientific expertise and market knowledge to improve the performance of their work for clients they work with. They provide an excellent service at every stage of the life cycle of a product or drug development process.
(Senior) RegulatoryandStudy Start-Up Specialist (m/f), Swiss
Switzerland
May 24
Wir suchen ab sofort einen dynamischen SSU Associate (m/w) der für unseren Kunden, einer renommierten CRO office based im Herzen der Schweiz tätig wird. Sie haben mind. zwei Jahre Erfahrung im Bereich Study Start-Up und bringen zudem Leaderfahrung mit und hatten bereits Erfahrung als direkter Ansprechpartner für investigator sites? - Dann bewerben Sie sich jetzt!............................................................................................ ...
Regulatory Affairs Manager (m/w)
Munich
May 24
Regulatory Affairs Manager (m/w)Office-based in MünchenAufgaben:- Planung, Koordination und Durchführung regulatorischer Aktivitäten für unsere Entwicklungsprogramme mit den involvierten Abteilungen (CMC Operations & Qualitätskontrolle, Präklinik, Klinik und Qualitätssicherung)- Teilnahme in Projektteams und Ansprechpartner gegenüber externen Partnern und Lohnherstellern in regulatorischen Fragestellungen- Erstellung, Zusammenstellung und Pflege von IMPDs, INDs, Briefing Books und Zulassungs ...
Regulatory Affairs Manager fuer Medizinprodukte – Pharmaunternehmen – Muenchen – bis zu 85,000 € plus Benefize
Germany
May 24
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.
Regulatory Affairs CMC Manager
Wales
May 24
Regulatory Affairs CMC Manager Wales£60 - £80 Per HourThe CompanyA leading, clinical-stage stem cell business where the primary objective is the development _of novel stem cell therapies targeting areas of significant unmet or poorly met medical need. ...
Senior Regulatory Affairs CMC Manager
Berkshire, UK
May 24
Senior Regulatory Affairs CMC Manager I am currently representing a Senior Regulatory Affairs CMC Manager position for a company located along the M4 Corridor. They are a large European headquarted Biopharmaceutical company working on innovative products in various interesting therapeutic areas.
Develop as a Senior CMC Regulatory Specialist
Denmark
May 24
Excellent opportunity in Copenhagen for you with a strong background in CMC!
Senior Regulatory Program Manager
Hertfordshire
May 24
Mary Tilston at CK Clinical is recruiting for a Senior Regulatory Program Manager to join a global, research-focused healthcare company at their site based in...
Regional Regulatory CMC Lead
Belgium
May 24
The Hydrogen Group has been appointed to search and select a Regional Regulatory CMC Lead, on behalf of a global biopharmaceutical company. Their main focus is on developing and researching innovative treatments that help to create solutions for different illnesses, specially the ones affecting the immune system. This is a great opportunity for an individual who desires to succeed within a challenging role to transform and bring something new.The role comes with an attractive salary.
Associate Director Regulatory Affairs
Rep. Ireland
May 24
Are you looking to work with Autonomy? Do you want to join a rapidly growing EU Regulatory Function?
Regulatory Affairs Specialist
Germany
May 24
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Regulatory Affairs Submission and Technical Specialist
Switzerland
May 23
I am currently partnered with a client of mine just outside the city of Basel. They are looking for the eCTD submission and Technical writing specialist that can be the key member of their team.. This role is with a Biological and organics molecule company. I need an experienced Regulatory Affairs Consultant with eCTD submission experience and Technical writing experience with this fantastic research and development company.
Regulatory Information Systems Analyst
Cambridge
May 23
Regulatory Operations - Publishing - Liquent InsightI am currently working with a large and growing biotech company based in Cambridge who are looking to grow their regulatory operations team (again!).
Regulatory Affairs - Clinical Trial Specialist - Paris Contract
Paris
May 23
If you feel you are the right candidate for this position, please contact me straight away on 0044 1293 776644 or Email your CV to troberts@barringtonjames.com Or is this role not for you...... Maybe a friend or colleague has the right attributes? Refer them to me and find yourself in the money still if they get THE JOB! €250 Reward!!!
Regulatory Affairs-BIOZIDE
Germany
May 23
Regulatory Affairs-BIOZIDEBei einem unseren weltbekannten Kunden in Nord Deutschland, einem Unternehmen in der Chemiebranche, bietet sich diese interessante Perspektive im Rahmen einer Festanstellung.
Team Leader/Senior CMC Regulatory Affairs Manager – Pharmaceutical consulting company - Karlsruhe – up to 80,000 €
Germany
May 23
We are looking for an experienced Regulatory Affairs Manager who wants to use his CMC knowledge in an international operating consulting company and lead a small team of Regulatory specialists. You can expect an open environment, exciting projects and excellent benefits.
Regulatory Executive
London
May 23
I am currently representing on of the best Pharmaceutical companies in the world. They are actively searching for a Regulatory Executive.
Regulatory Submissions Coordinator - Global Organisation - Munich
Germany
May 23
Just Pharma are currently assisting a global organisation in their search for an experienced Regulatory Submissions Coordinator to be office based in Munich Germany.
Regulatory Affairs Officer Submissions
Dublin
May 23
On behalf of our client, a growing pharmaceutical company, we are currently recruiting for Regulatory Affairs Officers for submissions. These are for permanent and 12 month contract opportunities.
Regulatory Affairs Officer Compliance
Dublin
May 23
On behalf of our client, a growing pharmaceutical company, we are currently recruiting for Regulatory Affairs Officers Compliance. These are for contract positions, approx 8 months duration
Regulatory Writer – Switzerland
Zürich
May 23
IM/130268/10Head of Regulatory Writing - Switzerland I am currently looking for an experienced regulatory writer, preferably from a CRO background, to join an exciting and dynamic agency in a new position.
Senior Associate, Clinical Trial Regulatory Services
Budapest
May 23
PAREXEL Hungary is looking for experienced Regulatory professional to join their Budapest team.
CMC Regulatory Affairs Manager
Germany
May 23
Regulatory Affairs CMC Manager – German Speaking – 12 Months Contract –Germany German Speaking Summary We are looking for a Regulatory Affairs CMC manager with commercial experience to work with a renowned pharmaceutical company. The successful candidate will have sound knowledge in CMC and experience working with chemical pharmaceuticals. This position is based in the Germany and the successful candidate must be able to communicate in German with immediate availability. ...
Regulatory Affairs CMC Manager Deutschland
Ulm
May 22
ein Erfolgreiches Pharmaunternehmen such fuer den Standort Ulm einen Regulatory Affairs CMC Manager. Die Stelle fokusiert auf Biologika und kommt mit unglaubliche weiterentwicklungsmöglichkeiten. ...
Senior Regulatory Affairs EU und DE Zulassungsprojekte
Stuttgart
May 22
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. ...
Head of Regulatory Writing – Switzerland
Zürich
May 21
IM/130268/09Head of Regulatory Writing - Switzerland I am currently looking for an experienced regulatory writer, preferably from a CRO background, to join an exciting and dynamic agency in a new position.
Senior Manager, Regulatory Operations
England
May 20
Our client is a rapidly growing international pharmaceutical company committed to bringing its portfolio of niche medicines to patients in more than 100 countries. Based in London they offer a good variety of work that only a SME can provide, giving them a unique family feel.
Senior Regulatory Affairs Manager
Germany
May 20
You will be working on project leadership involving European approval procedures & life cycle management. Role will be quite varied so requires candidates who are able to work in a complex environment and adapt to change well.
Junior Regulatory Affairs Manager
Germany
May 20
Role is varied so requires candidates who are able to work in a complex environment and adapt to change well. You will be part of a team of around 20, working in a fast paced environment and liaising with colleagues and clients globally.
Regulatory Systems Operational Analyst
England
May 20
A global pharmaceutical firm are looking for a Reg Systems Operational Analyst. Company have a wide range of products, including those targeted towards rare and chronic illnesses. They have strong portfolio of development projects, principally in the areas of gastroenterology and hepatology.
Regulatory Affairs Specialist - FOOD and Flavours
Germany
May 20
Regulatory Affairs Specialist - FOOD and FlavoursProgress your career and prove your skills !!!!My client, a global manufacturer of flavours and fragrances, is currently looking for a Regulatory Specialist to join its Global Regulatory Affairs Department in Germany. ...
Director Regulatory CMC, EU
New Jersey
May 20
The Hydrogen Group has been appointed to search and select a Director Regulatory CMC EU, on behalf of a global pharmaceutical company that focuses on producing innovative and generic treatments to be distributed over 20 countries globally. This is a great opportunity to deliver leadership and direction to the members of a Regulatory Affairs CMC EU team.The role comes with an attractive salary and comprehensive benefits package.
Senior Regulatory Associate
London
May 20
An 8 month contract opportunity has arisen to join the International Regulatory Affairs team based in either Cambridge or Uxbridge. Essential Duties and Job Functions   This position will be in the European HIV group in International Regulatory Affairs and will be responsible for the preparation of regulatory submissions for commercial. ...
Regulatory Labelling Consultant
Kent
May 20
This position reports to the locally based Regional Labeling Head, and may support other Hub Labeling Managers in terms of ongoing activities.Position PurposeThe Hub Labeling manager (HLM) is primarily responsible for preparation of local product documents (LPDs) and their associated Local Language documents (LLDs) for their assigned markets, updating the labeling documents on a timely basis according to internal SOPs and external regulatory requirements. ...
Regulatory Documentation Scientist
Hertfordshire
May 20
Mary Tilston at CK Clinical is recruiting for a Regulatory Documentation Scientist to join a global, research-focused healthcare company at their site based in Hertfordshire...
Associate Regulatory Advertising/Promo Director
USA
May 20
Responsible for performing regulatory review of advertising and promotional materials in the US. Provide expertise with respect to the requirements for promotional materials as set forth by FDA. Advise teams on best practices regarding planning and execution of marketing strategies. Assure that cross-functional advertising and promotion review teams are operating according to approved company processes. Responsible for the training of regulatory staff, as required.
Regulatory Affairs Director
West Chester
May 20
Directors and Associate Directors of Regulatory Affairs are responsible for: Setting regulatory strategy and translating these strategies into executable plans for specific departments/areas of responsibilityProviding direction and leadership to the Regulatory Staff in the development and implementation of global regulatory strategies and processes to assure timely commercialization of products in key markets in compliance with current and appropriate worldwide regulatory expectations. ...
Regulatory Affairs Specialist
Warsaw
May 20
The Regulatory Specialist will provide direct regulatory support to various projects and products, both new and existing. Responsibilities may include:  Support new, modified and currently marketed medical device products. This includes preparation of regulatory documentation for submission to regulatory authorities or internal regulatory assessment documentation. ...
REGULATORY: Latin American Head of RA, based US, Top 20 Co, Expansion Phase
US Based with Visa and Relocation
May 20
Please call me, Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (evenings/weekends) or on my USA Toll Free number +1 855 505 1382. Alternatively, you can email me on Matt.Greig@AdvRegulatory.com.
Regulatory Affairs / Director of Global Regulatory Intelligence / US based
US based
May 20
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 Senior Manager
Hertfordshire
May 20
i-Pharm Consulting are recruiting for…ROLERegulatory Affairs Senior Manager LOCATION: Hertfordshire SALARY: £60,000.00 - £70,000.00 per annum ROLE: Biologics focused company are looking for a Senior Manager to support ongoing expansion.Your role will focus primarily on development and maintenance.This includes compilation of PIPs, MAAs, CTAs (via VHP procedure) and submission of variations and renewals. ...
Regulatory Affairs Consultant
London
May 20
i-Pharm Consulting are recruiting for…ROLERegulatory Affairs Consultant LOCATION: Central LondonSALARY: £65,000.00 - £75,000.00 per annum ROLE: Biotech are looking for a Regulatory Affairs Consultant to assist with product licensing and maintenance of current product portfolio.As a permanent consultant your duty will be to develop strategy to ensure all products are compliant with EU guidelines and gain approval in a timely fashion. ...
Regulatory Affairs Operational Manager – Global Pharma – Exciting pipeline and Award Winning Portfolio – New York / New Jersey
USA
May 20
We are currently recruiting for a Regulatory Affairs Operational Manager to join our dynamic team and help with the development of our extensive pipeline. The Regulatory Affairs Operational Manager will oversee submissions.
Regulatory Affairs Director – Global Pharma – Award Winning Product Portfolio – NJ/NY
USA
May 20
We are currently recruiting for a Regulatory Affairs Director to join our award winning organization and focus on the Information Management of our extensive pipeline. The Regulatory Affairs Director will act as the information management expert.
Senior Manager, Regulatory Affairs
New Jersey
May 19
Skills Alliance is currently partnered with a leading global pharmaceutical company based in NJ that is looking to build out its regulatory team and bring...
Regulatory Affairs Project Manager
North London
May 19
i-Pharm Consulting are recruiting for…JOB TITLERegulatory Affairs Project Manager LOCATION: North LondonSALARY: Negotiable with Excellent benefitsROLE: One of the most innovative Biological company in the UK is looking for an experienced Regulatory professional to project manage product licensing related activities and also to maintain their current product portfolio. ...
Regulatory Affairs Project Manager - consultancy work - Surrey
Surrey
May 19
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
Director of Quality and Regulatory Compliance
South East
May 19
Director of Quality, Regulatory and Compliance required to lead Regulatory and Quality Compliance activities across multiple sites for the world’s foremost provider of health care...
Regulatory Consultant
IRELAND
May 19
Regulatory Consultant Job type: 11- month Fixed-Term Contract with the strong possibility for extension/ turning permanent Location: Dublin, Ireland Salary: €50,000-€60,000 per annum
Emerging Markets Regulatory Affairs Director \ International Regulatory Director
England
May 19
Emerging Markets Regulatory Affairs Director \ International Regulatory Director Location: Cambridgeshire - flexibility for 1 day per week home working. Benefits include extensive uplift which can be taken as additional cash
Head of Regulatory Affairs (Global)
Part home, part office based - UK, South East
May 19
Our growing, bio-pharmaceutical client is looking to appoint a Head of Global Regulatory Affairs. This is a leadership role in which the Head of Global Regulatory Affairs is responsible for all regulatory matters across the portfolio of existing medical and device products, as well as advising on business development opportunities from a regulatory perspective.
Global Head Regulatory Affairs
UK - London, Home Counties - Home based
May 18
My start-up Bio-Pharmaceutical client is looking to appoint a Head of European Regulatory Affairs. This is a leadership position, the Head of Global Regulatory Affairs is responsible for all regulatory matters across the portfolio of existing medical and device products, as well as advising on business development opportunities from a regulatory perspective.
Regulatory Affairs Supervisor
West Lothian
May 18
Job Title: Regulatory Affairs (RA) Supervisor Location: Lothian, Scotland Duration: Permanent Salary: £35k - £55k depending on experience + benefits package Start date: After your notice period Job details: Lead the Regulatory Affairs and Labelling departmentsDefine RA strategy for new productsFoster close working relationships with Regulatory Affairs departments throughout GermanyNetwork with other RA experts within the medical device industry to maintain expertise in best practiceDrive opt ...
Regulatory Inspection Compliance Manager
Home based (UK)
May 18
A leading global pharmaceutical company is currently looking for a permanent home-based Regulatory Inspection Compliance Manager to join their team.
Regulatory Affairs Manager (m/w) ATMPs
Berlin
May 18
Regulatory Affairs Manager (m/w) ATMPsOffice-based in BerlinAufgaben:- Ansprechpartner für alle zuständigen Behörden (v. a. ...
Regulatory Manager Europe (m/w)
Hesse
May 18
Regulatory Manager Europe (m/w)Office-based in Hessen- Develop the Regulatory strategy for new and for licensed products in Europe for applications via centralized and national procedures (DCP, MRP).- Communicate and ensure the implementation of the European Regulatory strategy in global teams. ...
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PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.