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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Regulatory Affairs Manager
Rep. Ireland
May 25
We are currently seeking applications on behalf of our client for the role of Regulatory Affairs Manager. A new position within the company, lots of autonomy, great opportunity!
Regulatory Affairs Scientist - Biotech
Cork
May 25
Regulatory Affairs Scientist A leading innovative global Biotech company is currently seeking a Regulatory Affairs Scientist to join their expanding business in their Cork site. This company is committed to further developing its growing portfolio of pharmaceutical products. Their products are marketed to almost 150 countries worldwide and this is a fantastic opportunity for someone looking to progress their career within regulatory affairs. ...
Regulatory Group Lead
Wexford
May 25
I have an immediate opening for a Regulatory Affairs Group Lead with a leading medical device company based in Wexford. This is a fantastic opportunity to join a leading medical device company in a Senior Regulatory Affairs position
Regulatory Affairs Manager - Needed ASAP
Berkshire
May 23
If working in a fast-paced environment with a wide variety of innovative class I to III devices at the forefront of the industry is where you see yourself, get in touch now!This is a great opportunity within regulatory affairs to join a world leading medical device company based in South East UK on an interim. Join an international regulatory affairs and quality team and gain the opportunity to develop your career on the global platform. ...
Senior Manager of Regulatory Affairs-CMC
Seattle
May 23
A growing pharmaceutical Company headquartered in the Seattle, Washington area is looking for a Sr. Manager of Regulatory Affairs-CMC.  This position offers unprecedented growth opportunities,...
ASAP - The Regulatory Program Manager – 6 months freelance roll
Belgium
May 22
The Regulatory Program Manager will be responsible for Global Regulatory Team (GRT) support.Will represent Regulatory Program Management (RPM) at the GRT translates the Regulatory strategy into realistic and executable Regulatory deliverables with clear assumptions based on GRT input. Works out Regulatory scenarios to support decision making in line with Regulatory and Compound Development Team (CDT) strategy. Will support early risk identification and development of mitigation strategies. ...
Senior Regulatory Affairs Officer
London
May 22
My client, a large pharmaceutical company, is looking for an experienced Regulatory Affairs professional to join they Project Management team. The company is bringing through some of their major pipeline products and are looking for new professionals to join their team. The successful candidate will have exposure to a wide range of Regulatory skills and will be look to be developed within the company.
CMC Regulatory Affairs Consultant – CMC, Contract, Europe – Global Pharma – Bucks
Berkshire, Middlesex, Buckinghamshire area
May 22
Regulatory Affairs, CMC, Contract – Fantastic new contract has opened up for a 6 month contract to join this established, top pharma as a CMC Regulatory Affairs Consultant. The positon, based from their HQ in Buckinghamshire, will see you responsible for CMC Dossier submissions in Europe. The role will be reviewing full dossiers from US submissions, amending as appropriate and ensuring successful completion for EU regulations.
CMC Regulatory Consultant – CMC Dossiers, EU, Global Pharma – Buckinghamshire
Berkshire/Buckinghamshire region
May 22
CMC Consultant, Regulatory Affairs, Contract – An excellent contract for 6 months has become available within this growing, Top 15 pharma business for an EU CMC Consultant. The position is office based in Buckinghamshire, with focus in EU CMC dossier review, working closely with US counterparts and filings for FDA. Requires those with proven background of EU orientated dossier work, able to take ownership on this and review FDA submissions to ensure EU submission success.
Senior Quality and Regulatory Affairs Manager-Consumable Devices
Belgium
May 22
Due to rapid growth, my client, an international healthcare company with an outstanding reputation in the industry, is currently looking to grow their team and currently looking a Senior Quality and Regulatory Affairs Manager with strong experience with Consumer care Medical Devices products to be based in Belgium.
EDMS Regulatory Business Systems Manager - World leading Pharma - Central London
London
May 22
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
Regulatory affairs associate - EMEA work-Buckinghamshire
Buckinghamshire
May 22
To apply for this regulatory affairs associate please call Julie Cooper on :Julie@moaiccrecruitment.co.uk Alternatively please send CV to: Julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Cosmetics - Nottingham
Nottingham
May 22
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
Senior Regulatory Affairs Associate - AFRICA region- Whole submission experience - Cambridge- Excellent salary and bonus
Cambridge
May 22
To apply for this regulatory affairs associate please call Julie Cooper on 07951 082482 Alternatively please send his CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate - LATAM role
Cambridge
May 22
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or alternatively please send your CV to: julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Project Officer- Nottingham - CTA , CMC , IMPDs, Authoring ,early drug development , ethics - UK knowledge
Nottingham
May 22
To apply for this regulatory affairs project manager role you will need to either call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Seniore Regulatory Affairs Consultant - Munich - Biologics , CMC work - Admired consultancy
Munich
May 22
To apply for this senior regulatory affairs role please call Julie Cooper on 07951 082482 Alternatively please send your CV to: Julie@mosaicrecruitment.co.uk
Regulatory affairs manager - Netherlands - affiliate role - must speak Dutch
Netherlands
May 22
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 Associate - Affiliate role - Netherlands
Netherlands
May 22
To apply for this regulatory affairs associate role please call Julie Cooper on 07951 082482 Alternatively please send your CV to: ulie@mosaicrecruitment.co.uk
Regulatory Affairs Associate Manager - EU role - Based Uxbridge with one day travel
Uxbridge or Cambridge
May 22
To apply for this regulatory affairs associate manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs and Patient Safety - Team Leader
Amsterdam
May 22
Do you want a cross-functional position which would give you the possibility to work together with different and diverse departments? My client an innovative Pharmaceutical company with a very interesting and fast growing pipeline is looking for someone who is willing to take the next step to a leading function.
Senior Regulatory Affairs Associate - UK - ROW and EU role
Cambridge
May 22
To apply for this role please call Julie Cooper on 07951 082482. Alternatively please send your CV to :julie@mosaicrecruitment.co.uk
Regulatory Affairs Opportunities, Switzerland
Switzerland
May 22
Regulatory Affairs Opportunities for Pharmaceuticals, Switzerland, Zurich, Basel, Geneva and Bern
URGENT - Global Senior Regulatory Affairs Manager - Medicines
England
May 22
My Client, a top Consumer Healthcare company are aspiring to find the best Senior Regulatory Affairs Associate to work with them on a global level.
EXCLUSIVE - Head of Regulatory Licensing and Compliance
England
May 22
I am currently working with possibly the BEST opportunity to come into your life. My client is one of the worlds leading consumer healthcare organisations. Their innovative thinking towards the marketplace has allowed them to become a force to be reckoned with in the pharmaceutical industry.
Regulatory Affairs Manager CMC (daily rate contract)
Buckinghamshire
May 22
Daily rate contract role: Regulatory Affairs Manager CMC required by client in Bucks until end of year - highly competitive daily rate payable!!
Regulatory Affairs Manager, Gloucester, Dynamic
Gloucestershire
May 22
A family owned but extremely well established chemical business is looking for a Regulatory Affairs Manager, to take on a dynamic permanent position.The company is in a great position at the moment and for over a century now have been growing with an impressive international reach, but the culture and feel of a smaller company. The successful candidate will be given the opportunity to liaise with various other departments
Start Up Manager - Regulatory Submissions Manager / CRO
Budapest
May 22
Clinical Study Start-Up Manager, Budapest, Hungary, JOB SUMMARY Project Manager for Clinical Study Start Up is required by a Global CRO, the role is office based in Budapest, Hungary. You will have worked for several years in Clinical Research and will be familiar with Study Start-up and Site Activation activities. ...
Global Pharma - Regulatory Affairs Associate - Sydney
Sydney
May 22
Global Pharmaceutical Company - Regulatory Affairs AssociateSydney$70,000 - $90,000 plus benefitsOur client are currently the fastest growing pharmaceutical company in Australia in terms of both profit and growth. They have won several awards and have numerous successful brand names. Coming into 2015 they have a solid pipeline with several of the leading drugs in the market.
CONTRACT - Senior Medical Writer - Regulatory/Clinical
England
May 21
For a confidential consultation call Meghann Price on 0044 (0) 207 255 6665 or email your CV to meghann.price@secpharma.comContract/Freelance Senior Medical Writer - Home-basedRegulatory/Clinical
Regulatory Affairs Manager (m/w)
Hamburg
May 21
Regulatory Affairs Manager m/wOffice-based in der Nähe von HamburgEin dynamisch wachsendes, international tätiges Pharmaunternehmen mit Sitz in Hamburg sucht einen Regulatory Affairs Manager.Aufgaben:? Erstellung und Pflege von Zulassungsdossiers und Qualitätsdokumenten.? Vorbereitung und Durchfürung von Zulassungsverfahren.? Verantwortung für das Lifecycle-Management? Mitarbeit in verschiedenen interdisziplinären Projektgruppen. ...
Regulatory Affairs Specialist – CMC – Belgium
Belgium
May 21
A small and growing pharmaceutical company is looking for a regulatory affairs specialist with focus on CMC. You can use your experience in redaction of CMC variations, registrations and renewals but also gain more experience for pharmaceuticals used in different therapeutic areas.
Regulatory Medical assistant – Independent Role – Belgium
Brussels
May 21
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 - Immediate Start
Berkshire
May 21
If working in a fast-paced environment with a wide variety of innovative class I to III devices at the forefront of the industry is where you see yourself, get in touch now!This is a great opportunity within regulatory affairs to join a world leading medical device company based in South East UK on an interim. Join an international regulatory affairs and quality team and gain the opportunity to develop your career on the global platform. ...
Regulatory Affairs CMC Director
Switzerland
May 21
Regulatory Affairs CMC Director - Small Molecules - Leading Pharmaceutical Group
Senior Regulatory Affairs Specialist-Freedom To Shape Your Work
Antwerp
May 21
Senior Regulatory Affairs Specialist-Freedom To Shape Your WorkMy client, a company who specialise in Molecular Diagnostics is seeking a Senior Regulatory Specialist to join their rapidly expanding Regulatory team. With 2 new people already on board in the team, you will work together to drive the companies new products onto the global market.
Regulatory affairs submissions specialist - Regulatory Operations and Info Management - UK - London- Contract
London
May 21
To apply please send your CV to:julie@mosaicrecruitment.co.uk or call me on 07951 082482
Regulatory Affairs Liaison Manager- Switzerland
Schweiz
May 21
Regulatory Affairs Liaison Manager, Switzerland * You have at least 3 years experience in the area of regulatory affairs and you would like to work for a global biopharmaceutical company? * You have a good understanding of the entire regulatory affairs processes and have worked at a strategic level? * You would like to work for a market leader with innovative products and a very international atmosphere?Then I have a fantastic opportunity for you at a biopharmaceuticals company in Switzerlan ...
Mitarbeiter Regulatory Affairs (m/w)
Frankfurt am Main
May 21
Mitarbeiter Regulatory Affairs (m/w)Office-based im Raum FrankfurtVoll- oder Teilzeit, befristet bis Ende 2015Aufgaben:? Inhaltliche und formale Überprüfung von regulatorischen Unterlagen auf Plausibilität und Eignung für die Zulassungsdokumentation? Umgang mit Publishing Software und selbständiges Erstellen von eSubmissions? Eingabe von Daten in Datenbank? Vorbereitung und Unterstützung bei der Durchführung von Zulassungsverfahren und Einreichung von Änderungsanzeigen)Voraussetzungen:? Erfo ...
Regulatory Affairs Manager CMC - Raum Basel
Basel-Landschaft
May 21
Regulatory Affairs CMC Manager (w/m) Raum BaselFür ein mittelständisches Pharmaunternehmen im Raum Basel suche ich einen Regulatory Affairs CMC Manager (m/w). ...
Regulatory Affairs associate –Career development -Ireland
Republic of Ireland
May 21
My client are a global pharmaceutical company based in Ireland who are currently looking for a Regulatory Affairs associate to join their team on an initial 6 month contract. This is an excellent opportunity for learning new skills and taking on some excellent experience with the chance for repeat contracts.
Regulatory Affairs Officer – Global Pharma – Ireland
Republic of Ireland
May 21
My client is a large pharmaceutical company who are currently looking for a Regulatory Affairs Officer and kick start your career with Regulatory Affairs within Ireland. With this opportunity you will find an excellent chance to learn and develop different skill sets that will springboard your career.
Quality and Regulatory Officer-Strong IVD Pipeline-Netherlands
Rotterdam
May 21
Quality & Regulatory Officer-Strong IVD Pipeline-NetherlandsMy client, a Biotech company in the Netherlands is currently looking for a Quality & Regulatory Officer to join their team who focus on hematological cancer. In this role you will be exposed to the niche but growing area of IVD as well as working with some of the most innovative products on the market, with this company already having products on the market and future products to come.
Regulatory Affairs Manager, Zurich Area
Zürich
May 20
Regulatory Affairs Manager, Zurich Area, Broad role with very good commitment for growth and rewards- 140k+
Regulatory Project Leader Crops - Bulgaria, Greece
Brussels
May 20
Working with a recently established organisation when it comes to the Crop Protection industry, this is an organisation focusing on the marketing side of products but that also is moving towards a broader area of focus and responsibility. As a result of a new department being set up, there is a major recruitment process across a variety of levels and across all EU Offices. This organisation has a long term commitment to growth and has achieved a significant amount.
Associate Director for Regulatory Affairs, Biosimilars
Zürich
May 20
Associate Director for Regulatory Affairs, Biosimilars
Regulatory Specialist Agrochemicals - Brussels
Brussels
May 20
Working with a recently established organisation when it comes to the Crop Protection industry, this is an organisation focusing on the marketing side of products but that also is moving towards a broader area of focus and responsibility. As a result of a new department being set up, there is a major recruitment process across a variety of levels and across all EU Offices. This organisation has a long term commitment to growth and has achieved a significant amount.
Regulatory Medical assistant – Develop Skills – Belgium
Brussels
May 20
A growing pharmaceutical company is looking for a regulatory medical assistant who will support the regulatory and medical manager. This will be in the areas of regulatory, quality, medical affairs, pharmacovigilance and market access. Accordingly you can use your background 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 Manager
Portugal
May 20
My client is a leading bio-pharmaceutical company looking for an enthusiastic Regulatory Affairs professional to join their passionate and innovative team. The ideal individual would deal with the regulatory affairs activities in Spain and Portugal with direct support from the Portuguese Technical Director where you will be ensuring conformance to national and EU drug laws.
Regulatory Affairs Manager - CMC
England
May 20
An exciting opportunity has arisen for a Global Regulatory Affairs Manager to join their thriving team within a global biopharmaceutical organisation.
Senior Regulatory Affairs Manager
England
May 20
Our client is a global market leader in providing biopharmaceutical services. They have extensive therapeutic, scientific and analytics expertise within biopharmaceutical and health sciences.
Senior Regulatory Affairs Manager
England
May 20
A market leading bio-pharmaceutical consultancy company has an exciting new position for a Senior Regulatory Affairs Officer based in the city of London.
Regulatory Affairs Officer
England
May 20
This opportunity is for a leading biopharmaceutical services organisation that has helped develop or commercialize some of the top selling drugs on the market. They have a high focus on dedication to ethics and high quality in the pursuit of success in human measures.
Regulatory Affairs Officer
England
May 20
Our client is a global market leader in providing biopharmaceutical services. They have extensive therapeutic, scientific and analytics expertise within biopharmaceutical and health sciences.
Global Regulatory Affairs Manager
Portugal
May 20
My client is one of the most innovative and dedicated groups within the Pharmaceutical industry today who are looking to extend their Regulatory team on a global basis. The role will play an integral part of their development plans and would influence their product portfolio for years to come.
Global Regulatory Affairs Manager
Portugal
May 20
My client is one of the most innovative and dedicated groups within the Pharmaceutical industry today who are looking to extend their Regulatory team on a global basis. The role will play an integral part of their development plans and would influence their product portfolio for years to come.
Regulatory Affairs Projects – Continuous Growth
Netherlands
May 20
Gain a fantastic varied role within regulatory affairs with a leading organization based in South of the Netherlands. You will be working within a wide range of project from 250 clients within the biopharmaceutical, medical device and life science industry.
Regulatory Affairs pharmacist - France - entry level
France
May 20
Le candidat sera en charge de la validation des dossiers AMM génériques et leurs modifications dans le cadre de procédures centralisés, MRP et décentralisés. Bien d'autres responsabilités seront incluant le controle de la publicité, suivre quantitativement et qualitativement la production et l'approvisionnement etc... (Nous pouvons vous renseigner par téléphone pour les autres missions)
Senior Regulatory Affairs Specialist-Global Market Exposure-BE
Antwerp
May 20
Senior Regulatory Affairs Specialist-Global Market Exposure-BEA company who specialise in the field of Molecular Diagnostics are looking for a Senior Regulatory Specialist to join their Regulatory team. My client aim to be market leaders in their field of work and as such are looking to expand their market reach outside of Europe, offering you a position where you will always learn and develop new skills.
Regulatory Affairs Specialist - Orthopaedics
Hertfordshire
May 20
If you woke up this morning wishing you could work with an expansive portfolio of class I to III devices, look no further!My client are a renowned orthopaedics manufacturer that are looking for experienced regulatory affairs professionals to come on board as soon as possible to take part in a variety of projects within the medical devices area. ...
Regulatory Affairs Manager – Relocation Assistance – Austria
Austria
May 20
As Regulatory Affairs Manager you will be responsible for the quality part, mainly module 2.3 and 3, for international submissions. You will be working in life cycle development but also life cycle maintenance. In addition to working on submissions, renewals, and variations, you will be working on CMC strategies and how to improve the regulatory process. Another aspect to you work is the communication with regulatory agencies, including EMA and AGES.
Regulatory Writer- Global Pharma- Cambridgeshire
Cambridge
May 20
My client is looking for a Senior Regulatory Writer to join their Leading Pharmaceutical Company. This company are a global leader within the industry which means you'll be able to enhance your professional profile.Within this role you will have a range of responsibilities. You will be writing, mentoring junior members of the team and liaising with external vendors all to deliver a great quality of writing. ...
Trainee Regulatory Affairs (w/m) (München - Deutschland)
Munich / München - Germany
May 20
Shared Work – Shared Vision: The way we do business, a promised standard that includes ongoing support from a specialized team dedicated to meeting or exceeding our clients’ expectations. Zur Unterstützung unseres Regulatory Affairs Teams in Deutschland suchen wir zum schnellstmöglichen Zeitpunkt eine/n motivierte/n Trainee (w/m).
Quality and Regulatory Officer-Innovative IVD Products-Rotterdam
Rotterdam
May 20
Quality & Regulatory Officer-Innovative IVD Products-RotterdamI am looking for a Quality & Regulatory Officer to join a biotechnology company who focus on hematological cancer. In this role you will be exposed to the niche but growing area of IVD as well as working with some of the most innovative products on the market.
Start-up / Regulatory Associate, Prague Czech Republic
Prague
May 20
Site Start Up and Regulatory Specialist (Global Role)Location: Office based - Prague, Czech RepublicSeveral roles with different level of seniority available. Please apply if you are a Start-up and/or Regulatory speacialist or CTA, Clinical Trial Coordinator, In-House CRA with experience in Submissions.
Regulatory Affairs Managers wanted in Brussels, Belgium - Global CMC roles covering EU/US//Emg/Japan/LatAm
Brussels, Belgium
May 20
These exciting opportunities will allow you to take the CMC strategic lead for development and marketed products, managing the generation of high quality regulatory submissions .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 Global CMC Project Manager – Brussels -
Brussels, Belgium
May 20
Work on Global CMC projects - Have real autonomy, scope and responsibility for your own varied product portfolio - Receive excellent training & guaranteed career development. 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 Operations Consultant
Cambridge
May 20
This is a new job opportunity at a biopharmaceutical company focused on developing cancer treatments. They are currently recruiting for an experienced Regulatory Affairs Operations Consultant to join their expanding team in Cambridge. This is an exciting time to join this company who operate across the United States, Europe and other international markets and have an extensive pipeline of products under development. This is a 3 month contract job with the opportunity to extend. ...
Regulatory Affairs CMC Associate Director – Brussels – Strategic CMC role for EMEA regions Salary to 110,000 euros + Car + Bonus
Brussels, Belgium
May 20
Reporting directly into the Global Head of CMC, you will be the CMC lead for your projects, which includes a A Late stage development project & Supporting a Centralized MAA -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 Operations Consultant
Maidenhead
May 20
An internationally known biotechnology company situated in Berkshire and operating in over 70 markets worldwide is looking for a Regulatory Affairs Operations Consultant. The company specialises in neurological conditions and puts a great emphasis on teamwork and delivering biological products. This role will be based in Maidenhead and is a 6 month contract role with the possibility of an extension. ...
Regulatory Affairs Officer; exciting new permanent opportunity
North West
May 20
A great development opportunity has become available for a regulatory professional seeking new challenges in the fast moving generic market. My client is one of the largest generic companies in the UK with over 350 employees and a growing product portfolio; a company that values the importance of professional growth. The permanent Regulatory Affairs Officer position will be office based in the North West of England.
Clinical Study-Start up Specialist, Study Start-up, In-house CRA, Regulatory associate, CTA, Clinical Trial Associate – Spain OR Portugal
Spain
May 19
Clinical Study-Start up Specialist, Study Start-up, In-house CRA, Regulatory associate, CTA, Clinical Trial Associate – Spain OR Portugal Please contact Zoe Benningfield on 07896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential
Regulatory Affairs Manager
England
May 19
My client is looking for a Global Regulatory Affairs Manager to join their thriving team. This is an exciting opportunity that would require the successful individual to manage regulatory/technical projects for both internal and external clients. You will also be expected to provide strategic regulatory/technical consultancy on a variety of projects.
Senior Regulatory Affairs Manager (m/w) - Tuttlingen
Tuttlingen
May 19
Senior Regulatory Affairs Manager (m/w) der MedizintechnikOffice-Based in Tuttlingen, DeutschlandIhre Aufgabe• Maintenance and optimization of the quality management system• Assists in strength / weakness analysis of the Quality Management System• Responsible for compliance to all applicable standards• Review and approval of processes, creates/revises procedures and work instructions to ensure these processes are correctly documented• Serves as a checkpoint to ensure procedures are written i ...
Senior Manager Regulatory Affairs (m/w)
Berlin
May 19
Senior Regulatory Affairs Manager (m/w)Office-based near BerlinJob Description:? Lead, mentoring and overseeing project teams and assist with new hire decisions? Participation and organization of Scientific Advice Meeting with the competent authorities in Germanyand Europe? Coordination and oversight of all regulatory activities in Germany for assigned product groups anddevelopment projects of the team? Represent the team internally and externally? Delegation of tasks and projects within the ...
Regulatory Affairs Associate
Prague
May 19
Due to our success and expansions we are looking to recruit Regulatory Affairs Associate.
PW 6319 Regulatory Submissions Officer
London
May 19
Excellent opportunity for a life science graduate with some experience in either, Clinical Development / PV or Regulatory Affairs to join this leading global Pharma Company as Regulatory Submissions Officer. Responsibility will be for the tracking of PSUR submissions and you’ll establish and own the management of this on behalf of the organisation. Excellent administration and communication skills will also be required.
Regulatory Affairs Consultant-Exclusive Role-Medical Devices
Marseille
May 19
NonStop Medical Devices are currently exclusively searching for a regulatory affairs consultant for a market leading medical device company. With international offices this role can be based from either their site in the South of France of the London area in the UK. This is an exciting eight month project within the regulatory department with a key focus on process validation, sterilisation, cleaning and packaging.
Senior Regulatory Affairs - Varied Role
Netherlands
May 19
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.
Director EU Regulatory Affairs
Hampshire
May 19
EU Regulatory Strategy Lead - DirectorPermanent JobCompetitive negotiable salary + bonus and benefitsBased in Hampshire, UKCurrently recruiting are global specialty pharmaceutical company who are fast becoming major players in the industry. After a recent restructure and a massive last quarter with increased revenue of 30%, they are now looking for exceptional regulatory affairs professionals to support their up and coming pipeline of products. ...
Regulatory Senior CMC Manager, Spain
Spain
May 19
New role for a Senior Regulatory Affairs Manager.
Regulatory Senior CMC Manager, France
France
May 19
New role for a Senior Regulatory Affairs Manager.
Regulatory Senior CMC Manager, Germany
Germany
May 19
New role for a Senior Regulatory Affairs Manager.
Regulatory Senior CMC Manager, Portugal
Portugal
May 19
New role for a Senior Regulatory Affairs Manager.
Regulatory Affairs Specialist - Ophthalmology
Paris
May 19
Key words: Regulatory Affairs, Executive, Officer, Specialist, Associate, LCM, EU, Global, Ophthalmology, MAA, Contract, Interim, Freelance, Paris, France
Head of Regulatory Operations - Interesting Varied Pos. - NRW
Köln
May 19
A global well respected family owned organisation with offices in NRW are currently looking to take an experienced professional on for a very interesting and varied position in Germany. The role comes with a fantastic package, including a number of benefits you normally would not get such as flexibility on work times and possibility to work from home, on top of the usual monetary renumeration. ...
Regulatory Manager CMC
London
May 19
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 Affairs Professional- CMC
Dublin, Republic of Ireland
May 19
Our client a leading pharmaceutical manufacturing company now have an immediate requirement for a Regulatory Affairs Professional- CMC. This is a full time fixed term contract based in Dublin. Applicants should have a strong knowledge and experience of working with quality documentation for drug products and drug substances.
PV and Regulatory Associate –More Responsibilities- Belgium
Belgium
May 19
The international healthcare company is looking for a pharmacovigilance and Regulatory Associate to join and support the regulatory team. It is a small team where you can work closely together and divide different tasks. This is why you will combine regulatory and pharmacovigilance responsibilities. Accordingly you can use your experience, develop more skills and have variety in the day to day activities.
Regulatory CMC Senior Specialist, London
England
May 19
A fantastic opportunity to working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level. Currently I am looking for experienced regulatory specialist who are knowledgeable within the CMC field.
Regulatory Affairs CMC - Contract
Berkshire
May 19
My client, a global Biopharmaceutical company are searching for a Regulatory Affairs CMC Specialist, to start a 1 year contract, where you can either be based in Belgium or South East England. My client is looking for a consultant with a minimum of 5 years in industry. My client is offering a very competitive hourly rate for this role. For more information and to apply for to this role, please call Richard Williamson on 0203 327 3072 or apply via this advert.
Regulatory Manager - Home-based - Full Lifecycle
Home Based
May 19
Overview: Skills Alliance are currently working with a small but growing speciality pharmaceutical company to recruit an experienced Regulatory Manager who will be responsible to...
Senior Regulatory Affairs Specialist-Growing Regulatory Team-BE
Antwerp
May 19
Senior Regulatory Affairs Specialist-Growing Regulatory Team-BEMy client, a company who specialise in the field of Molecular Diagnostics are looking for a Senior Regulatory Specialist to join their Regulatory team. You will work within a team which is growing extensively to meet the needs of the companies desire to be market leaders on a global scale.
Regulatory Affairs Manager for API Registration in Frankfurt
Darmstadt
May 18
Seeking a regulatory affairs manager with experience in registering APIs to be used in the pharmaceutical industry, as well as more complex half-products ideally but not as main requirement. The best thing that this position offers in my opinion, is a close knit team of professionals that operate on a flat hierarchy model and help and support each other making each day much more pleasant and successful. ...
EU Regulatory Strategy Lead – Contract/Consultant, 6 months, Biopharma
Berkshire, Hampshire, Surrey, Switzerland
May 18
Unique contract opportunity to work as the EU Regulatory Affairs Strategy Lead for this global biopharma business. This position will see you as the key authority on European Regulatory activities, working across teams in submissions, CMC, variations and the full span to ensure successful completion of regulatory aspects. The position is office based in the Berkshire/Hampshire region (or Switzerland) and requires those with a proven background of delivering European strategy for reg activitie
EU Regulatory Product Strategy Lead – Contract, Director level, Global Biopharma, UK
Berkshire, Hampshire or Switzerland
May 18
Fantastic new opening for a 4-6 month contract has opened up for an EU Regulatory Product Strategy Lead to join this internationally respected Biopharmaceutical. To be based either in the Berkshire/Hampshire area or Switzerland this role requires those with extensive breadth of regulatory affairs exposure into submissions, CTAs, MAAs and regulatory strategy. If you are coming from a Regulatory Director or Consultant level this is a role not to be missed.
Regulatory Operations Manager - Permanent
England
May 18
ACTIVELY SEEKING PERMANENT REGULATORY OPERATIONS MANAGER IN OXFORDSHIRE AREA Requires 5+ years Regulatory Experience Position will involve management of all Regulatory Matters in UK reporting to Headquarters in USA
Senior Regulatory Writer- Global Pharmaceutical- Cambridgeshire
Norfolk
May 18
My client is looking for a Senior regulatory writer to join their global company. This company are a global leader within the industry which means you'll be able to enhance your professional profile. As well as this you can really grow here due the senior managements meritocratic minded nature.Within this role you will have a range of responsibilities. You will be writing, mentoring junior members of the team and liaising with external vendors. ...
Regulatory Affairs Manager Bei Lübeck, Deutschland FREELANCE
Norderstedt
May 18
Regulatory Affairs ManagerBei Lübeck, DeutschlandFREELANCEKlasse III ProduktAufgaben:• Produktzulassungen auf internationaler und nationaler Ebene• Durchführen von Design Dossies nach CE standard• Erstellen aller nötigen Dokumente für die internationale Registrierung • Erfahrung mit Risikoanalysen nach ISO 14971• Einhaltung von Zertifizierungsanforderungen für Medizinprodukten und deren Zubehör (MDD, FDA, PAL)• Abstimmung aller Tätigkeiten im RA Bereich, • Cross-Funktionen mit den jeweiligen ...
Regulatory Affairs Manager (m/w)
Berlin
May 18
Manager Regulatory Affairs (m/w)Office-based near BerlinJob Description:Regulatory Affairs? Prepare, review, and approve regulatory documents including study reports, investigational and/or marketing application subsections, and regulatory authority communications (letters, meeting requests, briefing documents, etc.). Facilitate communication with clinical staff, subject experts, medical writers, project manager and team members with respect to technical sections of regulatory documents. ...
jobs : 100 +
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