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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Associate Director Regulatory Afffairs - Contract Job
Hillingdon, England, United Kingdom
Apr 18
Purpose

• Demonstrably the affiliate expert in quality and regulatory, acting as the primary point of contact for all affiliate quality and regulatory issues. ...
Senior Manager EMEA Regulatory Policy and Intelligence Job
Hillingdon, England, United Kingdom
Apr 18
POSITION Senior Manager EMEA Regulatory Policy & Intelligence
SUPERVISOR Director Regulatory Policy & Intelligence
DEPARTMENT EMEA Regulatory Affairs
PREREQUISITES Understanding of IT tools and information systems
Understanding of EU regulatory legislation and guidance required. Scientific discipline degree required; Extensive pharmaceutical industry or health authority experience, with recent experience in regulatory intelligence preferred.. ...
Manager, Regulatory CMC International Job
Hillingdon, England, United Kingdom
Apr 18
POSITION Manager, Regulatory CMC International
SUPERVISOR Senior Manager, Regulatory CMC
DEPARTMENT Technical Operations
PREREQUISITES BS/BA degree in Scientific Discipline (Masters or higher preferred) with extensive experience in the pharmaceutical industry or in CRO, including specialist CMC regulatory experience.

Responsibilities will include, but are not limited to, the following:

1. ...
Contract Regulatory CMC Associate - Large Pharma - UK
See main text
Apr 17
This is a fantastic opportunity for an experienced CMC contractor to join one of the world’s leading Pharmaceutical companies.
Senior Manager, Regulatory CMC
Central London
Apr 17
You will be an integral member of a small pharmaceutical & regulatory affairs team managing projects through the provision of strategic, technical & regulatory support during the introduction of new pharmaceutical products & line extensions as well as the maintenance & lifecycle management of the company’s range of marketed products throughout Europe. This is a permanent position, full-time & office based in London.
Regulatory Affairs Specialist, East Anglia, Contract
Cambridgeshire
Apr 17
A medical device client of mine have an urgent need for a Regulatory Affairs Specialist on a contract basis. The role is based in East Anglia and will be a 3-6 month position with the 6 months being more likely due to the work load. They are looking for someone to start immediately so the shorter the notice period you have the better. The role will be based in the UK however there will be some travel to Paris so would need someone who is able to do this. ...
Regulatory Medical assistant–Independent Role–Belgium
Brussels
Apr 17
A growing pharmaceutical company is looking for a regulatory medical assistant who will support the regulatory and medical manager. In this role you will have the chance to organise your work really independently and take initiative. Your work will be valued and you will have the possibility to develop yourself more.
Regulatory Affairs Manager - Orthopedic Devices - Frankfurt
Frankfurt am Main
Apr 17
Are you a Regulatory Affairs Professional? My client is offering a fantastic opportunity with their product portfolio of medical devices
EU and Global Regulatory Development and MAA roles –Based in the UK, Switzerland, Belgium or The Netherlands – From Advanced
UK, Switzerland, Belgium or The Netherlands
Apr 17
Please have a read and let me know if any of these roles are of interest. If there another type of role in another location that would be more interesting/suitable for you, then please let us know as we work some of the world’s leading Pharmaceutical and Biotechnology companies based all over Europe If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 -
Regulatory Affairs Manager-Independent role-Devices-Heidelberg
Heidelberg
Apr 17
Are you a Regulatory Affairs Professional? My client is offering a fantastic opportunity with their product portfolio of medical devices
Manager Regulatory Affairs – kleines Unternehmen – Stuttgart
Stuttgart
Apr 17
Als Manager Regulatory Affairs sind Sie für die Betreuung von Zulassungen in Deutschland und der EU zuständig. Sie stellen sicher, dass die Inhalte des CTD den europäischen Richtlinien entsprechen. Weiterhin arbeiten Sie an nationalen und europäischen Änderungen und Verlängerungen sowie PSURs und stellen sicher, dass wichtige Zeitpläne eingehalten werden. Außerdem stehen Sie mit den Zulassungsbehörden in Kontakt und arbeiten an Produktinformationen.
Junior Quality and Regulatory, Medical Device Candidates Wanted
Netherlands
Apr 17
Junior Quality & Regulatory, Medical Device Candidates WantedDo you have a years experience in Quality Assurance or Regulatory Affairs in the Medical Devices sector? Are you looking to take the next step in your career? Do you speak Dutch and/ or French? With the market currently having a lot of junior roles I am looking to speak with motivated candidates to introduce to my globally known client portfolio.
Regulatory Affairs Manager - South East - Expanding Biotech in the M4 Corridor with an excellent pipeline for Oncology and Immunology
Berkshire, Maidenhead or Uxbridge
Apr 17
There are options available to work on Products in Phase I, II & III through to MAA for both Pharma and biotech (Monoclonal) products. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380
Regulatory Affairs Project Manager
Berkshire
Apr 17
This is a brilliant opportunity for a Regulatory Affairs Project Manager to join a renowned biopharmaceutical company who have approximately 25000 employees placed in over 170 countries, this particular role will be based in Berkshire. This diverse company who specialise in research and development focus on producing strong clinical performances, assessable patient benefits and economic value. ...
Vice President, Global Regulatory Consulting - UK
Camberley, Surrey, UK
Apr 17
Leads the global regulatory consulting organization. Responsible for driving business development and delivery of consulting projects to expand and grow the consulting group globally. In addition to the operational aspects of the job, also focuses on customer relations, business development, and marketing of the Company’s consulting services.
Regulatory Affiars EU and Global CMC roles –Based in the UK, Switzerland, Belgium or The Netherlands – From Advanced Regulatory
UK, Switzerland, Belgium and the Netherlands
Apr 17
Advanced Regulatory Search and selection specialize in Regulatory Affairs Recruitment in the UK and mainland Europe. Please find below a list Regulatory CMC roles based at our Pharmaceutical & Biotechnology clients in the UK, Switzerland, Belgium and The Netherlands at EU and Global levels. 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)207 801 3380
Regulatory Affairs Manager - UK
Chester
Apr 17
Salary: £50,000 - £60,000My client, an international leading medical devices manufacturer is currently looking for Regulatory Affairs Manager for a fantastic opportunity based in the north western region of the UK.This is a fantastic opportunity for someone who is looking for a change in their career whilst working for a leading company in this field. ...
European Pharma Development Regulatory Opportunity
England
Apr 17
Roche are at the forefront of developing groundbreaking new medicines and consistently push the boundaries of conventional thinking and embrace innovation across our business.  With a strong pipeline, we are looking for people to support global teams to develop and gain approvals for medicines in Europe and Rest of World countries.  We currently have opportunities for exceptional Regulatory Programme Managers to join our global team working specifically on our Oncology portfolio. ...
Regulatory Program Manager
England
Apr 17
Roche are at the forefront of developing ground breaking new medicines and consistently push the boundaries of conventional thinking and embrace innovation across our business.  With a strong pipeline, we are looking for people to support global teams to develop and gain approvals for medicines in Europe and Rest of World countries. We currently have an opportunity for exceptional Regulatory Program Manager to join our global team. ...
Regulatory Affairs Professional – Arabic speaking
Republic of Ireland
Apr 17
A company, with roots in the fast growing foods / agrochemicals sector, is looking for a Regulatory affairs professional. The markets you will be working on are the Middle East and North African markets. This will give you the opportunity to work from Ireland but keep using Arabic. As said before the market is a fast growing market which will give you a chance to grow as a regulatory affairs professional within the company.
Regulatory Affairs Specialist - Medical Devices
Berkshire
Apr 17
Regulatory Affairs Specialist - Medical Devices. Berkshire. Regulatory Professionals are pleased to be representing a genuine leader in the medical devices and diagnostics field in their search for a part-time Regulatory Affairs Specialist for a 9 month contract. The Regulatory Affairs Specialist will report into the Director of Strategic Regulatory Affairs for the UK and Ireland and will take responsibility of guaranteeing that the regulatory requirements are met throughout the UK and Ireland
Regulatory Affairs Specialist
Ireland
Apr 17
Regulatory Affairs Specialist. Galway - Ireland On-going contract - 0.5 FTE / Part Time An Exciting opportunity with an expanding Medical Device Manufacturers in Ireland has become available for an RA Specialist with a year or mores experience to join them on an on-going part time contractual basis.
Regulatory Affairs Global CMC Role - Great Salary and full Re-location Packages Available - South-East
South-East
Apr 17
These roles are good mix of strategic input, Global project management and cover development and marketed products. There are options available to become a technical specialist or move into people management.If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380
Regulatory Affairs Manager CMC for International and Emerging Markets – M4 Corridor - Take the lead for strategy and submissions and Gain Biologicals Exp.
South-East
Apr 17
Take the lead for International strategy and submissions for a Global Pharmaceutical company that continues to grow, develop and show innovation in how it brings new products to market. This role comes with a real career development plan and all the training you will need to climb that ladder to the next level of Director. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380
Regulatory Affairs CMC Manager / South-East / Join a Biologics company with a Great Pipeline
South-East
Apr 17
We have a new role based in the South-East for a Top Ten Biotechnology company who require a CMC regulatory Affairs manager to cover development, registration and approval/post approval activities. This is a varied and highly strategic CMC role based at a Global Head office. Contact Theo Moore on +44(0)207 801 3384 to apply for this role or send your CV in confidence to CV@advregulatory.com
Regulatory Medical assistant – Variety – Belgium
Brussels
Apr 17
A growing pharmaceutical company is looking for a regulatory medical assistant who will support the regulatory and medical manager. Those tasks will consist of responsibilities within regulatory, quality, pharmacovigilance and market access. This means that you can use your experience but also learn more about several areas within the pharmaceutical industry. Even more it will give you a lot of variety in the day to day activities.
Regulatory Affairs Specialist
Germany
Apr 17
Regulatory Affairs Specialist Position zentral in Baden-WürttembergFür unseren Kunden suchen wir ganz aktuell einen Spezialisten für die Zulassungsabteilung.Das als Technologie und Marktführer bestens positionierte Unternehmen, bietet Ihnen ein spannendes, abwechslungsreiches Arbeitsumfeld, in dem Sie gefördert werden aber auch viel Raum für eigene Ideen haben. Zu Ihren Aufgaben wird die Bearbeitung von weltweiten Zulassungen unserer medizinischen Produkte gehören. ...
Project Manager, Regulatory Affairs (Post Licensing) - EMEA-116915
England
Apr 17
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...
Associate Director, Regulatory Affairs, Emerging Markets
Zürich
Apr 17
Associate director for regulatory affairs, strategic role helping to develop fast growth across the world. Dynamic environment working with innovative products!
Regulatory Affairs Manager – Emerging Markets – Munich
Munich
Apr 16
As Regulatory Affairs Manager you are responsible for submission, variation and renewal in the MEA (Middle East and Africa) region. You will be in touch with local affiliates and implement new regulatory guidelines. Further, you will be working on regulatory strategies to make submissions more efficient and male sure they are done according to the time frame. You will be the contact person for people within the company and you will be in touch will local health agencies.
Senior Regulatory Affairs Associate, Zug, Global Submissions
Zürich
Apr 16
Senior Regulatory Affairs Associate, Global Submissions, Broad role with very good commitment for growth and rewards- 130k+
Regulatory Affairs Managers – Diversity
France
Apr 16
A fast growing start-up, near London, with the financial backing of a stable company is looking to hire a regulatory affairs manager. The position of regulatory affairs manager focusses on life cycle management and some new products that are in the pipeline. This will give you diverse work. Furthermore, the company is part of a bigger group and will have the advantage of financial stability the bigger companies have and the advantage of growth and expansion the start-ups have.
Regulatory Affairs Consultant – Fulltime
Netherlands
Apr 16
With the Regulatory Affairs Department rapidly growing my client is looking for an experienced professional who wish to expand their experience in Regulatory Affairs by working in a challenging role as senior consultant. You will work within an inspiring environment of a leading consultancy company providing you with the opportunity to work in a wide variety of projects and be in direct contact with clients.
Regulatory CMC Director, Biologics, Major Project
Geneva
Apr 16
Regulatory CMC Director, Biologics, Major Project, Early Development, Strategic Role Leading a Key Product, 200k+
Senior Regulatory Affairs Associate LATAM
San Francisco
Apr 16
Responsible for execution and management of regional life-cycle submissions for all company products as well as new product registrations by focusing on local needs of Affiliate Drug Regulatory Affairs (DRA) teams to ensure right first-time submissions to Health Authorities.
Freelance Senior Regulatory Affairs Associate
London
Apr 16
My client, a market leading research-based pharma company in the South East, have a new contract opening for a Senior Regulatory Affairs Associate. This is a great opportunity to work with a driven team on a strong pipeline spanning multiple therapeutic areas.
Regulatory Compliance PV
England
Apr 16
A senior person within Regulatory Compliance PV is wanted to join my client, a leading global biopharmaceutical company. You will be joining their International Compliance team.
Regulatory Affairs Project Manager (m/w)
Frankfurt am Main
Apr 16
Manager (m/w) Regulatory ManagementOffice-based in der Nähe von Frankfurt a.M. ...
Regulatory Compliance PV Manager
Cambridge
Apr 16
An exciting opportunity has arisen for a Regulatory Compliance PV Manager to join a global biopharmaceutical company based in Cambridge. A very patient focused company, who scientific research has resulted in 15 marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. ...
Regulatory Affairs Associate
Rep. Ireland
Apr 16
With 5 commercial products, 7 more in the pipeline and over half a billion dollars of revenue, a global footprint in 40 countries, and a personal connection to our patients, BioMarin is the recognized industry leader in rare disease development. Come work in an entrepreneurial environment where you’ll have the resources and infrastructure combined with visibility and opportunity to tangibly impact patent’s lives and the future of our company. This is your chance to be part of something amazing!
Regulatory Project Manager – CRO – Greater London
England
Apr 16
I am currently seeking for a commercial aware and energetic Regulatory Project Manager to join a well-established CRO company on permanent basis.
Head of Quality/Regulatory - Medical Devices - Munich
Munich
Apr 16
My client, an international leading medical devices company in the field of Cardio/Respiratory is currently looking for a Director in Regulatory Affairs and Quality Assurance for a fantastic opportunity based near the beautiful town of Munich in Germany. This is a fantastic Regualtory/Quality opportunity for someone who is looking for a change in their career whilst working for a leading company in this field. ...
Regulatory Platform/Hub Leader
Cambridge, UK
Apr 16
We are seeking a Regulatory Platform/Hub Leader. You will be responsible for managing the Regulatory Affairs Platform/Hub.
Senior Regulatory Affairs Executive
London
Apr 16
Looking to progress your career in Regulatory Affairs to the next level? My client is growing at an astronomical rate and require a Senior Regulatory Executive to assist in the expansion.
Senior Regulatory Affairs Executive
Kent
Apr 16
Fantastic Opportunity for experienced individuals within Regulatory Affairs! Amazing career development and progression.
EDMS Regulatory Business Systems Specialist - World leading Pharma - Central London
London
Apr 16
To apply for this EDMS Regulatory Affairs System role please call Julie Cooper on 07951 082482 or send your CV to- julie@mosaicrecruitment.co.uk
Senior Manager, Global Regulatory Affairs MEA
Bavaria
Apr 16
SEC is currently collaborating with a major global generics company (part of a bigger healthcare group) whose affordable medicines are currently available to 90% of the world's population.I have personally been tasked with find an inovative, stategic thinking regulatory professional to join their Global Regulatory Affairs Department within the MEA team at Senior Manager Level. ...
Regulatory Manager CMC–Growing Company–SW Germany
Germany
Apr 16
My client is looking for a Regulatory Manager CMC who is looking for an opportunity to work on a broad range of challenging and rewarding projects as part of an experienced team. Working for Germany's leading service provider you will have the chance to build strong relationship with the biggest pharmaceutical companies .
Regulatory Affairs Associate –Benelux– Belgium
Brussels
Apr 16
The company is a global market leader in generic products and looking for a regulatory affairs associate responsible for the big product portfolio. They want someone who is fluent in Dutch, French and English because you will have contact with local authorities. At the same time you can use your languages and strengthen your network.
Regulatory Affairs Manager – Benelux – Belgium
Brussels
Apr 16
The pharmaceutical company is a global market leader in generic products and is now looking for a regulatory affairs manager who will be responsible for a big product portfolio. The focus of this manager will be on the Benelux which gives you the chance to use your knowledge about the local regulations and use, strengthen your network with the local authorities.
Regulatory Affairs Associate Director – Brussels - Take the lead for Centralised filings and EU/ROW strategy – Salary to 120,000 + Car + Bonus
Brussels, Belgium
Apr 15
As a high performing organisation, my client is committed to growing and developing their people and within this International multi-cultural regulatory department you will find challenges and opportunities to keep you interested, motivated and developing for many years to come.If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380
CMC Manager / Regulatory Affairs CMC Technical Specialist Basel, Switzerland Varied and Broad-based Global CMC role
Switzerland
Apr 15
Utilise your CMC experience in a role which will cover all aspects of Global product registrations and lifecycle management for an extensive product portfolio covering all major dosage formulations. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380
Regulatory Affairs Snr Manager Wanted for a Top Ten 20 Pharma Company – The Netherlands – Salary 90,000 + Bonus -
The Netherlands
Apr 15
Provide strategic leadership for MAA’s, lifecycle & development projects - The culture here is friendly, positive and has a real feel of self-improvement and you will be taught/mentored by a Snr RA Director with a number of successful RA strategies and submissions behind him. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore on Matt Grieg on +44 (0)207 801 3380
Regulatory Director (FDA/EPA) New Projects-Pharma
Atlanta
Apr 15
Our client is a global pharmaceutical firm looking to hire someone for this role immediately. Ideal Candidate Will Be Responsible For: Management of EPA Pesticide...
Study Start-Up and Regulatory Specialist (EMEA)
West London
Apr 15
Study Start-Up & Regulatory Submissions Specialist (EMEA)Office based in West LondonAn international CRO with fantastic prospects for growth following a buy-out in 2012 and due to their expertise in the delivery of late stage projects is seeking a Regulatory & Study Start-Up Submissions Specialist to join their growing SSU & Regulatory team on a permanent basis. ...
Regulatory Affairs Manager –People Management– Belgium
Brussels
Apr 15
The pharmaceutical company is a global market leader in generic products and is now looking for a regulatory affairs manager who will be responsible for a big product portfolio. You will lead a team of regulatory affairs, manage their workload and establish an evaluation system according to objectives and priorities of company. This means that you can transfer your knowledge and feel good about developing other people.
Regulatory Affairs Manager - Hands On Exp.
Chester
Apr 15
Salary: £50,000 - £60,000My client, an international leading medical devices manufacturer is currently looking for Regulatory Affairs Manager for a fantastic opportunity based in the north western region of the UK.This is a fantastic opportunity for someone who is looking for a change in their career whilst working for a leading company in this field. ...
Regulatory Affairs Specialist - Devices - UK
Chester
Apr 15
Salary: £30,000 - £40,000This is a great opportunity within regulatory affairs to join a global manufacturer based in North West UK who are looking to expand their regulatory division. Join an international regulatory affairs and quality team and gain the opportunity to develop your career on the global platform. Our client produce class I through to class III medical devices further allowing you to develop your career with high risk products. ...
Regulatory Affairs Consultant
North Holland
Apr 15
Regulatory Affairs ConsultantBen jij commercieel ingesteld, sociaal en pas jij je snel aan in een nieuwe omgeving? Dan ben jij de persoon die we zoeken. Voor onze organisatie in Noord-Holland ben ik op zoek naar Regulatory Affairs Consultant.FunctieomschrijvingAls consultant krijg je de kans om in verschillende organisaties en aan verschillende projecten te werken. Deze projecten lopen uiteen en dekken alle aspecten van Regulatory Affairs, afhankelijk van je kennis, ervaring en interesse. ...
International Regulatory Affairs – Markets and Compliance Manager - STRONG COSMETICS EXPERIENCE NEEDED - Midlands
Midlands
Apr 15
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Cosmetics - Nottingham
Nottingham
Apr 15
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
EDMS Regulatory Systems Specialist - World leading Pharma - Central London - Global Regulatory Affairs
London
Apr 15
To apply for this EDMS Regulatory Affairs System role please call Julie Cooper on 07951 082482 or send your CV to- julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - Must have Middle East and Africa experience - UK - Bucks - 12 months FTC
Buckinghamshire
Apr 15
To apply for this senior regulatory affairs associate please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Regulatory affairs submissions specialist - Regulatory Operations and Info Management - UK - London
London
Apr 15
To apply please send your CV to:julie@mosaicrecruitment.co.uk or call me on 07951 082482
CMC Senior Regulatory Affairs Associate - EU role - Cambridgeshire
Cambridge
Apr 15
To apply for this senior regulatory affairs associate please call Julie Cooper on 07951 082482 or alternatively please send your CV to;julie@mosaicrecruitment.co.uk
Regulatory Affairs manager - UK/IRE (Food/Nutritional Supplements)
Buckinghamshire/Hertfordshire
Apr 15
I am currently representing a global food and nutritional supplements company who are actively searching for a Regulatory Affairs Manager to lead a team in the UK and Ireland markets. The role will be leading a team of 2 people developing and maintaining regulations with their whole portfolio of products in the local markets.
Regulatory affairs Manager
London
Apr 15
My client who is a new start up consumer focussed organisation are currently recruiting for an EU Regulatory Manager. They are based in Central London and looking for somebody who has a deep knowledge of Regulatory Affairs working with Consumer Healthcare products. ...
Senior Regulatory Affairs – Varied Role
Leiden
Apr 15
Gain a fantastic varied role within regulatory affairs with a leading consultancy organization based in West of the Netherlands. You will be working within a wide range of project from 250 clients within the (bio) pharmaceutical, medical device and life science industry.
Senior Regulatory Affairs Executive
Berkshire
Apr 15
Senior Regulatory Affairs Executive. Berkshire A leading Global Pharmaceutical company currently requires an experienced Regulatory Affairs professional to join their Consumer division. Working from Pre-Approval to Post-Approval on new and established products, this job offers broad responsibility in a position considered to be the first step into management within the company.
Regulatory Manager CMC–Leading Company–SW Germany
Germany
Apr 15
Working as a Regulatory Manager CMC you will have the opportunity to work for a rapidly expanding company where career progression can happen very naturally. You will also have the opportunity to build strong and lasting relationships with the largest pharmaceutical companies in Germany.
Regulatory Manager CMC–Growing Company–SW Germany
Germany
Apr 15
As a Regulatory Manager CMC you will be working for one of Germany's leading service providers for the global pharmaceutical industry. You will have the unique opportunity build contacts with leading pharmaceutical companies and rapidly expand your business network.
Regulatory Affairs Associate – EEMEA Markets
Basel, Switzerland
Apr 15
Fast paced role with direct responsibility for executing regulatory strategy for lifecycle submissions in EEMEA markets.
Regulatory Records Manager
Basel area, Switzerland
Apr 15
Our client is a leading biopharmaceutical company with more than 30 operating affiliates worldwide and specialises in respiratory and orphan diseases. The Regulatory Records Manager will work within the Global Drug Regulatory Affairs department, managing the paper records for Global Clinical Development with an emphasis on adherence to Good Clinical Practice (GCP).
Clinical and Regulatory Start-up Lead - Europe
Bulgaria
Apr 15
Premier Research are a growing global CRO focused on delivering high quality clinical research projects to their diverse client base. With industry leading expertise in Paediatrics, Analgesia, Oncology and CNS we are looking for career focused individuals who want to be a part of our growth.
Regulatory Labelling Manager for a Top Consultancy
Frankfurt am Main
Apr 14
My client is a top consultancy with offices in Frankfurt that is able to offer a very diverse work life due to the large number of clients that rely on their services. They are currently looking for a regulatory labelling manager to work on some of the most interesting such projects in Germany. Apply for the chance to enjoy the security of a permanent position with a fixed salary as well as the diversity of contracting. ...
Regulatory Manager for an ethical top company Frankfurt
Frankfurt am Main
Apr 14
My client is ethical top 10 pharmaceutical company focused primarily on the well-being of patients and on the fight against the very serious diseases that are inconveniencing their lives. The already very successful head of regulatory affairs is looking to expand their senior management team by taking on an experienced regulatory affairs manager. You will take over high level regulatory intelligence activities and define pro-active strategies that take into account future regulations. ...
Head of Regulatory - Food / Feed products Frankfurt
Frankfurt am Main
Apr 14
Recruiting for a head of regulatory affairs with a very unique and interesting company that is active in the field of special additives for nutritional and pet feed products. The role will allow you to work closely with senior business partners as well as the VP of regulatory affairs of the company which will allow you to learn and expand your skill set, effectively adding value to your profile and opening you up for more diverse positions in the future. ...
Regulatory Affairs Specialist - 1 year contract
Galway
Apr 14
Major Duties: * Maintain an excellent understanding of global medical device regulations for specific jurisdictions as assigned * Provides regulatory support to Design & Development, operations, quality, sales & distribution functions, advises the requirements for the target markets and the outputs required to meet the applicable regulatory requirements * Determines, plans and prepares regulatory submissions for specific target markets for new products, product changes and re-registrations a ...
Regulatory Submissions Specialist (CTA/MAA)
Cambridgeshire
Apr 14
My client, a market leading research-based pharmaceutical company, have a new contract opening for a Regulatory Submissions Specialist to join their driven and passionate team as they support multiple MA applications in the EU and Switzerland over a busy upcoming period.
Regulatory Operations Associate II
Cambridgeshire
Apr 14
My client, a market leading research-based pharmaceutical company, have a new contract opening for a Regulatory Operations Associate to join their driven and passionate team as they support multiple MA applications in the EU and Switzerland over a busy upcoming period.
Regulatory Affairs Consultant – Various Projects
Leiden
Apr 14
With the Regulatory Affairs Department rapidly growing my client is looking for an experienced professional who wish to expand their experience in Regulatory Affairs by working in a challenging role as senior consultant. You will work within an inspiring environment of a leading consultancy company providing you with the opportunity to work in a wide variety of projects and companies.
Regulatory Affairs Manager - Austria
Austria
Apr 14
Our client is looking for a Regulatory Affairs Manager with one year of industry experience to join their Regulatory team based in Austria. As an established global pharmaceutical company they are looking for someone who has a good understanding of the industry and post-approval activities. ...
Regulatory Affairs Manager (home-based)
South East England
Apr 14
A global pharmaceutical company is looking for a Regulatory Affairs Manager in the South East.The purpose of this role will have to deliver and maintain competitive licences for European commercial brands. The ideal contractor will ensure timely submission and approvals of all licensing applications and compliance with European regulatory requirements. The ideal candidate would need to have at least 5 years of experience in regulatory affairs. ...
Regulatory Writer Home-Based - Rare
City of London
Apr 14
Regulatory Writer Home-Based - Rare!!This 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 CMC Project Manager
Stockholm
Apr 14
Currently recruiting is an international specialty pharma company who have products marketed in over 60 countries across a broad range of therapeutic areas. They are looking for a Regulatory CMC Project Manager to join them at their office in Stockholm on a FTC basis at first with a guaranteed permanent role when this is finished. They are looking for someone with the following qualifications:• Authoring of module 3 document, both 3.2.S and 3.2.P with the main focus on 3.2. ...
Regulatory Affairs Lead - Medical Devices
Gloucestershire
Apr 14
My client is searching for a Regulatory Affairs Lead to join their exciting company. As a leading supplier of single use Medical Devices to the global market and they have an innovative and very exciting product portfolio, which has been updated and expanded in line with technological advances. At the core of their philosophy is the drive to develop products, which satisfy the current and future needs of both patients and healthcare professionals.
Regulatory Executive
Hertfordshire
Apr 14
An excellent opportunity has arisen for a Regulatory Executive with 1-2 years of regulatory experience to join a fast joining pharmaceutical company based in the Hertfordshire area.
Regulatory Affairs Manager - Innovative Devices - Freiburg
Freiburg im Breisgau
Apr 14
Are you a Regulatory Affairs Professional? My client is offering a fantastic opportunity with their product portfolio of medical devices
Regulatory Affairs Specialist - Medical Devices - Tuttlingen
Tuttlingen
Apr 14
My client is looking for a Regulatory Affairs Specialist to join them due to expansion...
Regulatory Affairs Manager for EU and global Projects – CMC focused role – develop your expertise in Mabs, Vaccines and ATMPs - Lausanne
Lausanne, Switzerland
Apr 14
This role with develop your CMC biotech experience to the highest level as you work with EU and Global clients on strategies and submissions, whilst learning from some of the industry’s most experienced CMC Biotech regulatory technicians. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 -
Regulatory Affairs Associate Director - Netherlands - EU and International strategic leadership role - Excellent Portfolio - Expanding Pharma Company
The Netherlands - close to Amsterdam
Apr 14
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 send your CV to cv@advregulatory.com or call Theo Moore on Matt Grieg on +44 (0)207 801 3380
Regulatory Affairs Associate Director / EU and Global Strategy and Project Management - Belgium
Brussels, Belgium
Apr 14
My client has exciting products and challenging project work. It’s a company with a very good growth rate and has a promising future. They have lots of products in the pipeline which means more growth and exciting times are ahead. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs CMC Global Regulatory Liaison roles MAbs and Vaccines Great Salary, re-location and Career Development Belgium
Brussels
Apr 14
If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Regulatory Affairs Senior Manager CMC Biologicals Brussels Provide Strategic leadership for CMC Bio projects Excellent pipeline
Brussels
Apr 14
My client is seeking professionals who can show leadership, high level influencing and persuading with an excellent cross-cultural awareness and understanding of the regulatory framework.Excellent salary and a broad based role. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Managers wanted in Basle Switzerland- Global CMC roles covering EU/US/Japan/Emg/Japan/LatAm – Salary to 150,000CHF + Bonus
Switzerland
Apr 14
These exciting opportunities will allow you to take the strategic lead for marketed products, managing the generation of high quality regulatory submissions required for the filing of technical changes to health authorities globally. 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)207 801 3380
Regulatory Affairs Senior Global CMC Specialist / Switzerland – Global Projects – Excellent Salary – Fantastic Company…
Switzerland
Apr 14
This Global CMC department provides leadership for commercialized products and your role will be to operate as the Regulatory project lead for interactions with all major global regulatory agencies. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Regulatory Affairs CMC Bio Snr Manager role for a global biotech company – From PI to PIII and registration - Brussels
Belgium, Brussels
Apr 14
This will be an EU (into Global) role and the pipeline for Biologicals in all stages of development (from PI to PIII and registration) and the snr management team are very highly rated within the industry and have a reputation for allowing others to take real project ownership. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380
Regulatory Affairs Global CMC Project Manager – Switzerland -
Switzerland
Apr 14
You will need at least 5 years of Regulatory affairs CMC experience and be ready for a role where you have real autonomy, scope and responsibility for your own varied product portfolio. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380
Regulatory Senior CMC Manager
England
Apr 14
New role for a Senior Regulatory Affairs Manager. I am looking for an international regulatory CMC professional who will be responsible for human pharmaceutical products, involving both small and large molecules, injectable devices, investigational and marketed products.
jobs : 100 +
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