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The latest Regulatory jobs - BETA

Jobs: (Regulatory)

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Regulatory Affairs Consultant
Reading
Dec 9
My client, a leading Pharmaceutical based in Maidenhead is looking for a talented and experienced Regulatory Affairs professional to join their already established team.
Head of Regulatory Health care UK – OTC/Consumer health
England
Dec 9
Head of Regulatory Health care UK – OTC/Consumer health
Head of Regulatory Health care UK – OTC/Consumer health
England
Dec 9
Head of Regulatory Health care UK – OTC/Consumer health
(Senior) Regulatory Affairs Consultant – Pharmaceutical consulting company - Netherlands – up to 80,000 €
Netherlands
Dec 9
We are looking for a Regulatory Affairs Specialist, who wants to use his knowledge in an international operating consulting company and help pharmaceutical organization to achieve the best results. You can expect an open environment, exciting projects and excellent benefits.
Regulatory Affairs Consultancy Germany
Germany
Dec 9
Our client, one of the fastest growing consultancies within Regulatory Affairs in the Pharmaceutical Industry is currently looking for Regulatory Affairs professionals that have good experience with EU-submissions and Regulatory Operations.The company is known for its international community, relocation support, variety of global clients and excellent career progression opportunities. ...
Director Regulatory Affairs for several indications – global biopharma - Hessen
Germany
Dec 9
We are looking for an experienced Regulatory Affairs Specialist, who wants to use his knowledge about global strategy development in one of the biggest biopharmaceutical organizations worldwide. You can expect an open environment, life-changing projects and excellent benefits.
Regulatory Affairs Manager CMC Munich
Germany
Dec 9
Unser Kunde, ein rasch wachsendes, globales und innovatives Unternehmen, das sich nicht nur auf pharmazeutische Produkte, aber auch auf Nahrungsergänzungsmittel spezialisiert, sucht momentan nach einem Regulatory Affairs Manager für sein Team in München.Sie würden in einem relativ kleinen Team arbeiten und daher sehr vielseitige und zahlreiche Aufgaben haben. Darüber hinaus, würden Sie sich daher auch schnell weiterentwickeln können. ...
Regulatory Data Analyst
Troy
Dec 9
Here is a chance to join one of the most globally known pharmaceutical organisations, who are looking to hire a Regulatory Data Analyst based in USA. This job is at a top 10 pharmaceutical company that works across a range of industries from medical devices to pharmaceutical and consumer goods, operating in over 60 countries. ...
Regulatory Affairs Manager, Biologics
Zürich
Dec 9
Regulatory Affairs Manager, Biologics, Top Tier Pharma, New Local SubmissionsExcellent opportunity to join one of the top local affiliates working with a current blockbuster drug and some upcoming future potentials! Specifically, this role covers large and small molecule products in pre and post approval with Swissmedic. With this in mind, it can be a very interesting role for someone wishing to expand on their product/scientific experience and to be involved with newer submissions. ...
Regulatory Affairs Associate III
Sausalito
Dec 9
A worldwide, research-based biopharmaceutical company, focusing on areas spanning infectious diseases, oncology and liver disease, are looking to hire a Regulatory Affairs Associate III to work at their California site. With over 5000 worldwide professional staff, this company has an outstanding reputation for bringing lifesaving medicines to market within areas of high unmet medical need. ...
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Senior Regulatory Consultant
London
Dec 9
A leading global pharmaceutical company has a new vacancy for a Senior Regulatory Consultant to join their expanding London team. The company has a superb pipeline and operates in over 90 countries around the world.  Job role:  Oversees as well as executes all regulatory activities of multiple projects including one highly complex project for assigned marketed product(s) of responsibility.Manages direct reports to support scope of project work. ...
Associate Director - Global Regulatory Affairs
London
Dec 9
ProClinical are currently recruiting on behalf of a leading global pharmaceutical company that specialises in multiple therapy areas. They are currently looking to recruit a Associate Director - Global Regulatory Affairs to work in London. The organisation offer an excellent rate of pay and have a strong reputation as an excellent company to work for. ...
Senior Manager, Regulatory Operations
San Francisco
Dec 9
Job descriptionManager/Sr. Manager, Regulatory Operations Manager/Sr. Manager, Regulatory is responsible for managing the logistics, preparation, quality assurance, and delivery of regulatory submissions in accordance with Regulatory agency requirements, company standards, and timelines. The Manager/Sr. ...
Regulatory Champion Lead
Warsaw
Dec 9
PURPOSE   We seek for candidates providing regulatory support and oversight for our operational team.   Responsibilities Collate regulatory document- and process requirements for countries under responsibility. Assist with creation and/or review of country-specific regulatory documentation to enable study initiation and maintenance, as required. ...
EU Regulatory Project Manager - Get the ground running - Home
Netherlands
Dec 9
I am currently working for an agrochemical company that is starting to develop his presence in the European Market. To support this growth, they are looking for an experienced regulatory candidate, who can become part of the company and get the ground running from the start. You have the chance to work from you home-office and will be in charge of:
Regulatory EMEA Director with a Global Top 20 Pharma company - Expansive role with opportunities to become a GRL - Netherlands
The Netherlands
Dec 9
These are great roles with a great company, offering excellent salaries and full re-location packages. The culture here is one of visibility and real product responsibility but with real regulatory support operational and strategic support available. Contact Theo Moore on +44 207 801 3384 or email your CV in confidence to CV@advregulatory.com
Regulatory Affairs Global CMC Director - Cover EU, US, Japan, Emg and LatAm – Based in Brussels - Great Salary, Bonus, Car and LTI Package
Brussels
Dec 9
Coordinate and drive global regulatory CMC strategy for complex submissions and determine and drive the execution of regional CMC regulatory plans in line with the global regulatory strategy. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Associate Director, Regulatory Affairs
Buckinghamshire
Dec 9
An excellent opportunity has become available for an experienced Regulatory Affairs professional to join an extremely successful Pharmaceutical company at Associate Director level. Within this role you will sit within the development group contributing to the global development of new products and supporting marketing authorisation applications, and gaining approval of line extensions and variations.
Global Regulatory Affairs CMC Director – Brussels – Strategic Global CMC with Team Leading - Great Salary + Car + Bonus + LTis
Brussels
Dec 9
Advanced Regulatory are now recruiting for a highly innovative and hugely successful pharmaceutical client who are expanding and developing their Global CMC department. To have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Publishing Consultant “CONTRACT ROLE”- The Netherlands – 12 months Excellent rate for a Global Pharma Co.
The Netherlands
Dec 9
This is an excellent role where you will be joining a pro-active and highly regarded Regulatory operations team for a leading global Pharmaceutical company based in The Netherlands. This is an excellent role where you will be joining a pro-active and highly regarded Regulatory operations team for a leading global Pharmaceutical company based in The Netherlands.
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Regulatory Affairs EU Liaison - Next step become a GRL in Oncology – The Netherlands – Mid and late stage development roles - Competitive salary
The Netherlands
Dec 9
Regulatory Affairs EU Liaison role - Next step GRL – The Netherlands Mid and late stage development roles where you take the lead for Centralised Submissions and Global Strategy...!!! 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 Officer Compliance
Dublin, Republic of Ireland
Dec 9
On behalf of our cn. lient, a growing pharmaceutical company, we are currently recruiting for Regulatory Affairs Officers Compliance. These are for contract positions, approx 8 months duration
Senior Regulatory Affairs Associate
West Sussex
Dec 9
A senior regulatory affairs associate opportunity with an exciting, global pharmaceutical company to join the regulatory affairs team and help to manage the full product...
Senior Regulatory Manager - Personal Care
Manchester
Dec 9
RECRUITING - Senior Regulatory Manager Personal careBoasting interest and involvement in a number of industries and secotors, our client has a confident diverse evenue pipeline. In current economic climate such offerings mean job security and a chance to be exposed to a number of different areas. Our clients Consumer Products range is involved in the production of raw materials for personal care and comsetics. ...
Regulatory Affairs CMC Manager
Frankfurt am Main
Dec 9
An exciting opportunity for a CMC Regulatory Affairs Manager to join a dynamic, fast growing Pharmaceutical consultancy and work with the Regulatory Affairs team in...
Regulatory Affairs Associates NEEDED-Secure Perm Role-CH
Basel
Dec 9
An immediate need has come in with our client based in Basel for a regulatory affairs associate. This is a great, secure permanent role where you will be joining a reputable medical device company. Our client are looking for enthusiastic regulatory affairs professionals who have an understanding of the medical device regulations; looking to develop their career on an international scale. ...
Senior Regulatory and Site Services Specialist
Belgium
Dec 9
Our successful and dynamic team in Belgium is currently looking to expand. Are you searching for an exciting new role? Do you have any experience in start-up and regulatory affairs? Then this is a fantastic opportunity for you! We are looking to recruit a Senior Regulatory and Site Services Specialist - office based in Leuven
Global Director Regulatory Affairs – global pharma company – Munich – up to 130,000 € plus bonus
Germany
Dec 8
We are looking for an experienced Senior Regulatory Affairs Manager who wants to use his knowledge about strategy development in a global researching pharmaceutical organization in Munich. You can expect an open environment, life-changing projects and excellent benefits.
Technical Regulatory Specialist - QHSE, REACH
Cheshire
Dec 8
Our client is an impressive organisation experiencing significant growth over the past few years with their unique product manufactured using resins. Offering a broad product line and range with a strategy to diversify, this family grown business is keen to reward those who commit long term. This is provided through bonus and pension schemes that give the impression this company cares about its staff.
Regulatory Consultant
Surrey
Dec 8
Job Role:To allow the company to legally study, manufacture, market and supply medicines. To obtain, manage and maintain product Marketing Authorisations and Clinical Trial Authorisations (where applicable) in line with business goals and legal requirements. ...
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Regulatory Specialist - Safety Data Sheets, REACH
Essex
Dec 8
Regulatory Specialist - Safety Data Sheet, ComplianceWorking within an Global position, you will work as the department manager with 3-4 direct reports. Working across a diverse product range, this position will be the main point of contact concerning REACh and other EU regulations outside of REACh, being the subject matter expert.
Global Chemical Regulatory Manager - lead a team
Essex
Dec 8
Global Chemical Regulatory Manager - lead a teamWorking within an Global position, you will work as the department manager with 3-4 direct reports. Working across a diverse product range, this position will be the main point of contact concerning REACh and other EU regulations outside of REACh, being the subject matter expert.
Regulatory Officer - Cosmetics
North West England
Dec 8
Regulatory Officer - Cosmetics
Regulatory Affairs Associate–Benelux-Belgium
Belgium
Dec 8
A pharmaceutical company is looking for a Regulatory Affairs Associate to make sure the Regulatory documents for the Benelux are well prepared and submitted. Therefore you can use your current network and be the expert for the Benelux level. Besides you can still use your language skills.
Senior Regulatory Specialist household products
West Sussex
Dec 8
Senior Regulatory Specialist - household products!Working with a global FMCG company offering some of the most well known and leading consumer brands, this is an opportunity utilise your packaging experience and data management skills. In a cross category product position, you will play a central role in registrations within EU and partly responsible for global regulations.
Ass. Director Regulatory Affairs–TOP 3- Brussels
Brussels
Dec 8
A top 3 pharmaceutical company is looking for an Associate Director Regulatory Affairs to be responsible for the new registrations and life cycle management of a big successful portfolio. Their product portfolio just extended which gives the company even more good prospects. Therefore it is the right time to join the company and have a positive impact and be a part of the success.
Regulatory Scientific Affairs Beverage EU Global
Austria
Dec 8
Möchten Sie für ein weltbekanntes Unternehmen arbeiten?Möchten Sie Ihre Regulatory Affairs Karriere in der Lebensmittel- und Getränkeindustrie auf den nächsten Level bringen?Sehnen Sie sich nach Personalverantwortung, Herausforderungen, attraktives Gehalt und ein spannendes Arbeitsumfeld?Dann könnte das die richtige Gelegenheit für Sie sein!Eines der erfolgreichsten und bekanntesten Getränke-Hersteller sucht nach einem Leiter für sein Regulatory Affairs Team. ...
International Regulatory Affairs Manager Germany
Germany
Dec 8
Unser Kunde ist ein stabiles, mittelständisches Pharmaunternehmen mit mehreren Standorten in Deutschland. Das Unternehmen sucht momentan nach einem International Regulatory Affairs Manager für sein Büro in Nord-Deutschland.Das ist eine einzigartige Gelegenheit für Regulatory Affairs Spezialisten, die sich gerne im Bereich International und Global Submissions weiterentwickeln möchten, und sich nach einem familienähnlichen Betriebsklima sehnen. ...
Regulatory Electronic Submission Publisher – Brussels
Brussels
Dec 8
Regulatory Electronic Submission Publisher – BrusselsContract duration: 9 monthsBrussels, BelgiumThis fantastic job opportunity has arisen within one of the leading global healthcare companies providing innovative medicines, treatments and animal health products.The Electronic Submissions Publisher will work within the EMEA team in Brussels. ...
Regulatory CMC Lead, Global Emerging Markets
Maidenhead
Dec 8
Regulatory CMC Lead, Global Emerging MarketsMaidenhead, UKThe fantastic job opportunity has arisen within one the world’s largest biotechnology companies. You would be working to bring state-of-the-art medicines from the laboratory to the patient. With a history of over 30 years, the company has pushed the existing limits to deliver exciting therapies to medical teams around the world. ...
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Manager (Regulatory) PAREXEL Consulting (UK OR Dublin/Ireland)
Uxbridge
Dec 8
A manager within PC provides leadership and direction to associates, consultants and senior consultants, actively managing employee performance and development. A manager acts as a role model and provides or organizes coaching/mentoring and feedback to direct reports. A manager provides a broad range of consulting services and works within broad project guidelines to identify, refine, and address client issues and to achieve project objectives.
Head of Regulatory Affairs- West London
England
Dec 7
Head of Regulatory Affairs position now open in the West London area!
SEED Active Substance Regulatory - Home-Office
Netherlands
Dec 7
I am currently working for a fast upcoming agrochemical company, growing rapidly over the last couple of years. They have an extensive portfolio, being sold world-wide. To support their growth they are looking for an experienced regulatory candidate, who will be responsible for the registration of the Active Ingredients (AI) for their seed care portfolio.
REGULATORY AFFAIRS OFFICER EXCLUSIVE AND BRAND NEW - ENGLAND
England
Dec 7
REGULATORY AFFAIRS OFFICER **EXCLUSIVE AND BRAND NEW** - ENGLAND LEARN CTA AND CLINICAL APPLICATIONS
REGULATORY AFFAIRS OFFICER EXCLUSIVE AND BRAND NEW - ENGLAND
England
Dec 7
REGULATORY AFFAIRS OFFICER **EXCLUSIVE AND BRAND NEW** - ENGLAND LEARN CTA AND CLINICAL APPLICATIONS
Head of Regulatory Affairs Austria Global
Austria
Dec 7
My client is a global leader in the pharmaceutical industry. Due to their expansion, they are looking for a new Head of New Submissions and Renewals for their Regulatory Affairs department in Austria, close to the German and Italian borders. ...
CMC Regulatory Affairs Germany - no German needed
Germany
Dec 7
Our client, one of the fastest growing consultancies within Regulatory Affairs in the Pharmaceutical Industry is currently looking for Regulatory Affairs professionals that have good experience with CMC for their offices in Germany.The company is known for its international community, relocation support, variety of global clients and excellent career progression opportunities. ...
Regulatory Consultant (5134-1)
Surrey
Dec 7
A well-known international pharmaceutical company with sites around the globe is looking to hire a Regulatory Consultant. The company specialises in developing and producing medicines and vaccines for a wide range of therapeutic areas including oncology, cardiology and immunology. ...
Regulatory Project Manager
Massachusetts
Dec 7
ProClinical have a brilliant opportunity for a Regulatory Project Manager to be based in Massachusetts, USA. This job will be with one of the largest workforce management solutions companies in the world who specialise in multiple scientific and engineering sectors. Job Role:The Regulatory Project Manager will oversee a large, complex global approval database. ...
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Regulatory Consultant
Surrey
Dec 7
A well-known international pharmaceutical company with sites around the globe is looking to hire a Regulatory Consultant. The company specialises in developing and producing medicines and vaccines for a wide range of therapeutic areas including oncology, cardiology and immunology. Job Role: Accountable for supporting initial and post approval submissions for country acceptability in terms of content, according to local regulations and requirements for assigned markets. ...
Regulatory Affairs Associate Director
Boston, US
Dec 7
Regulatory Affairs Associate Director Location - Boston Salary $110,000 - $130,000 per annum plus extensive benefits package Do you want to work for an innovative Pharmaceutical company with a Biotech Focus?
Regulatory Affairs Associate
Newbury
Dec 7
Regulatory Affairs AssociateNewbury, United KingdomThis fantastic job opportunity has arisen within one of the leading global healthcare companies delivering cost-effective healthcare solutions.As a part of the role you would be responsible for coordination and preparation of local technical and administrative documents for regulatory submissions as well as reviewing for submission readiness. ...
Active Substance Regulatory Manager - Home-Office
Belgium
Dec 7
I am currently working for a fast upcoming agrochemical company, growing rapidly over the last couple of years. They have an extensive portfolio, being sold world-wide. To support their growth they are looking for an experienced regulatory candidate, who will be responsible for the registration of the Active Ingredients (AI) on a EU level.
Regulatory Records Associate
England
Dec 7
> An excellent opportunity has arisen within our Medical Directorate for a Regulatory Records Associate.  You will be responsible for the management of regulatory records associated with marketing authorisations and CTAs held by Roche Products Ltd in compliance with GxP and meeting the access and retrieval needs of the Regulatory Affairs group. ...
Senior Regulatory Affairs Associate-12 Month Contract – Sydney
Sydney
Dec 7
A Senior Regulatory Affairs Associate is required for a mid sized pharmaceutical company
Head of Regulatory Affairs- Expanding CRO UK
England
Dec 6
Renown CRO I am representing is currently offering a newly created opportunity as Regulatory Affairs Director.
Senior Regulatory Affairs Manager (m/w)
Basel
Dec 6
Regulatory Affairs Manager (m/w)Office-based in BaselMy client is an international top-10 pharmaceutical and biotech company. For their EU headquarters in Basel, I am looking for an experienced Regulatory Affairs Manager to manage all regulatory activities (full lifecycle) for a specific therapeutic area. ...
Biologics Regulatory Affairs Project Manager
Switzerland
Dec 6
A famous Swiss consulting life science company is looking for a Biologics Regulatory Affairs Project Manager to join its team in Switzerland. Do you like to work in a multicultural environment? Are you solution orientated and strong communicator? Then maybe you are suitable for this position! Let me please tell you more about it.
Lead, Global Regulatory Affairs, Advertising and Promotion
Zürich
Dec 6
A Market Leading Global Biopharmaceutical Company with a strong, innovative pipeline are looking to strengthen their post-marketed Regulatory Affairs team at their European headquarters in Zurich. Currently there are multiple new vacancies as the emphasis for management of products in the Oncology area grows. The primary focus within these positions would be a focus on local, post-marketed Regulatory Requirements for promotional and marketing materials in international markets.
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Senior Regulatory Affairs Specialist-Career Progression-Belgium
Mechelen
Dec 6
This is a great opportunity for an experienced regulatory affairs professional to develop their career with a market leading medical device and diagnostic company. Our client are supportive and invest in their employees; providing you with the perfect platform to develop your RA career on an international scale.
Regulatory Affairs Associate
Paris
Dec 6
One of the world’s largest pharmaceutical company is hiring!If you are specialized in regulatory affairs and you want to work for a great working environment company with a variety of missions, this job is for you !Your main responsibilities: • Provide and maintain strategic regulatory affairs advice and guidance• Develop and support regulatory activities • Serve as a program regulatory lead within the team• Responsible for relationships an successful partnership internally and externally Yo ...
Regulatory Affairs Senior Manager
London
Dec 6
Regulatory Affairs Associate Berkshire Would you like to work for award winning company? Do you like to work in a stable team with experienced and highly skilled professionals? Are you looking for a company who provide extensive training opportunities and further development?
Regulatory Affairs Associate
Berkshire
Dec 6
Regulatory Affairs Associate Berkshire £25,000 - £30,000 per annum Would you like to work for award winning company? Do you like to work in a stable team with experienced and highly skilled professionals?
Senior Vice President of Safety and Regulatory
London
Dec 6
Skills Alliance have entered into an exclusive, retained partnership with a global clinical trial services provider. We are seeking to appoint a Senior Vice President...
Manager Drug Regulatory Affairs (m/w)
Karlsruhe
Dec 6
Manager Drug Regulatory Affairs (m/w) - Sponsor - Vollzeit
BRAND NEW REGULATORY AFFAIRS QUALITY ASSURANCE MANAGER – BELGIUM (QARA)
Belgium
Dec 6
**BRAND NEW** REGULATORY AFFAIRS QUALITY ASSURANCE MANAGER – BELGIUM (QARA)
Senior Intern, Regulatory Submissions
Madrid
Dec 6
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Senior Intern/Regulatory Submissions Trainee to join our Clinical Operations team. ...
Regulatory Affairs CMC Specialist
Amsterdam,Netherlands
Dec 6
As the RA Specialist you will support the department activities, executing regulatory compliance activities regarding CMC (Chemistry, Manufacturing & Control) matters within the Global regulatory Affairs.
Regulatory Affairs CMC Manager
Frankfurt am Main
Dec 5
An exciting opportunity for a CMC Regulatory Affairs Manager to join a dynamic, fast growing Pharmaceutical consultancy and work with the Regulatory Affairs team in...
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Senior Regulatory Consultant - CTAs - HOMEBASED
Home Based
Dec 5
Skills Alliance have partnered with a global pharmaceutical company in order to find a Senior Regulatory Consultant who specialises in the strategy and submission of...
Regulatory Affairs Senior Associate
London
Dec 5
A growing pharmaceutical company based in Central London is looking to add a Regulatory Affairs Associate to their UK and IR team to support their...
Global Regulatory Affairs Director - Biotech
Netherlands
Dec 5
Global Regulatory Affairs Director - Biotech - International function
Regulatory Submissions Coordinator
München (81249)
Dec 5
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team! POSITION SUMMARY Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. ...
Regulatory Submissions Coordinator/Start Up Specialist
Milano
Dec 5
POSITION SUMMARYMedpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 40 countries across the globe. ...
Regulatory Affairs Manager
Vaals
Dec 5
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team!Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Affairs Manager to join our Medpace Medical Device team. ...
Clinical Study Start Up Specialist (Regulatory Documents)
Buckinghamshire
Dec 5
Minimum 12 month contract paying a competitive daily rate for a study start up specialist responsible for managing and coordinating all start-up activities leading to site activation.
Hamburg/Hannover Regulatory Affairs CMC Global
Germany
Dec 5
Unsere Klienten suchen momentan nach Regulatory Affairs Spezialisten in der Nähe von Hamburg und Hannover im Bereich CMC, Global Submissions und Generika. Es handelt sich um mehrere offene Stellen bei diversen Unternehmen (von Familienunternehmen bis Big Pharma).Ich spezialisiere mich nur auf Regulatory Affairs in Deutschland und Österreich, und habe zahlreiche Vakanzen, die Sie interessieren könnten. ...
EU Regulatory Affairs Manager, Basel, CP/DCP
Basel
Dec 5
EU Regulatory Affairs Manager, Basel, CP/DCP
Medical and Regulatory Information Specialist
Belgium
Dec 5
Medical & Regulatory Information Specialist- 6 Month contract- Immediate Start- Belgium Level: Medical Information & Regulatory Information Specialist Languages: English, Dutch French Contract: 6-12 Months contract Salary: Negotiable Location: Belgium, EU Summary We are looking for a Medical Information & Regulatory Information Specialist to join a leading pharmaceutical company. The successful candidate will have a strong g knowledge of Clinical research and development process. ...
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Regulatory Documents and Contracts Management Coordinator (RDCM Coordinator)
Buckinghamshire
Dec 5
Minimum 12 month contract for a regulatory documents and contracts management coordinator - would suit someone currently in a junior clinical regulatory / CTA / TMF role looking for further experience in pharma - competitive salary available
Head Regulatory Affairs–Benelux-Belgium
Brussels
Dec 5
A pharmaceutical company is looking for a Head Regulatory Affairs to lead the Benelux department. You will coordinate them and develop a regulatory strategy for the local registrations. Therefore you can use your current network and be the expert for the Benelux level. Besides you can still use your language skills.
CMC Regulatory Affairs Österreich / Top 10 Co
Austria
Dec 5
Mein Kunde, eines der erfolgreichsten und bekanntesten Unternehmen in der Pharmaindustrie in Österreich, sucht momentan nach einem Gruppenleiter für seine CMC Regulatory Affairs Abteilung. ...
Regulatory and Start Up Specialist 1 (f/m) - office based in Brussels
Brussels
Dec 4
PURPOSEPerform tasks at country level associated with Regulatory, Start-up (RSU) and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements andcontractual/budgetary guidelines. May participate in feasibility and/or site identification activities. ...
Medical Writer (Regulatory)
New York
Dec 2
Medical Writer (Regulatory) Location: Greater Philadelphia Area Salary: Competitive Industry: Pharmaceuticals Job Type: Contract – 12 months...
AD/Director Regulatory Affairs Needed for Expanding Pharma
Boston
Dec 2
AD/Director Regulatory Affairs Needed for Expanding PharmaOncology | FDAGreater Boston area$135,000 - $170,000 + bonus +complete benefits packageAn expanding pharmaceutical company is looking to  ...
Global Regulatory Affairs Leader
London
Dec 2
Good morning, Hydrogen Group partners globally with the Regulatory Affairs departments of Tier 1 Life Sciences companies and a precious opportunity has arisen within one of our global conglomerate Clients in the Consultancy area with offices based in London and Frankfurt. I am looking for a talented Global Regulatory Affairs Specialist who would enjoy stepping up in the career path and working in a Client Facing role as a Leader of a Global account and managing a team of specialists. ...
BRAND NEW REGULATORY AFFAIRS MANAGER – BELGIUM
Belgium
Dec 2
The company can offer you the chance to build a career in a way no other company can duplicate. They are innovative, fast-paced, results-oriented, and most importantly winners. If you want to join a winning team, then apply today for more information.
BRAND NEW REGULATORY AFFAIRS MANAGER – BELGIUM
Belgium
Dec 2
The company can offer you the chance to build a career in a way no other company can duplicate. They are innovative, fast-paced, results-oriented, and most importantly winners. If you want to join a winning team, then apply today for more information.
BRAND NEW REGULATORY AFFAIRS MANAGER – BELGIUM
Belgium
Dec 2
The company can offer you the chance to build a career in a way no other company can duplicate. They are innovative, fast-paced, results-oriented, and most importantly winners. If you want to join a winning team, then apply today for more information.
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Graduate Trainee, Regulatory Submissions
London
Dec 2
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Senior Intern/Regulatory Submissions Trainee to join our Clinical Operations team. ...
Senior Regulatory Affairs Manager (CMC) Opportunites - Germany
Germany
Dec 2
A Senior Regulatory Affairs Manager (CMC) role in Germany working for a growing and exciting pharma company. Looking for an experienced project manager within regulatory affairs to work in a permanent role. At least 3 to 4 years’ experience, 74a German drug law knowledge and proven track record of variation procedures and renewals of registrations and a background of full life cycle management.
Associate Director - Regulatory Affairs
Dublin
Dec 2
Associate Director of Regulatory Affairs - Dublin Leading Pharmaceutical Consultancy looking for an experienced Regulatory candidate to provide leadership and direction to staff as well as identifying potential future business opportunities. Need to be commercially savvy with a background in Regulatory Affairs and leadership. Good opportunity for someone to move into a Director role within 12 months. Must be eligible to work in Ireland. ...
Regulatory Labelling Consultant
Surrey
Dec 2
An excellent opportunity to join a global top ten pharmaceutical company within their Regulatory team. The company employs over 30,000 employees globally and are recruiting for a Regulatory Labelling Consultant to work at their offices in Surrey. ...
Global Head of Regulatory and Medical Affairs
Scotland
Dec 2
Following global expansion and several exciting new business wins, ClinTec International Global CRO actively recruiting for a Global Head of Regulatory and Medical Affairs to join our growing UK team. This is a permanent opportunity ideally based within our Glasgow HQ office, however flexible working may be possible.
Regulatory Affairs Manager
Scotland
Dec 2
Following a period of expansion, ClinTec International, Globa CRO, are looking to build a global Regulatory Affairs team and as such an exciting opportunity has arisen for a Regulatory Affairs Manager to join us on a permanent basis within our Glasgow HQ Office.
Senior Regulatory Affairs Manager
Zürich
Dec 2
Company DescriptionOur client is a multi-national pharmaceutical and biopharma company is looking for a Senior Regulatory Affairs Manager who will be based in Zurich....
Regulatory Affairs Specialist
Paris
Dec 2
Good morning, Hydrogen Group partners globally with the Regulatory Affairs departments of Tier 1 Life Sciences companies and a rare opportunity to work and specialise on global scope projects of Class 3 Medical devices has arisen within one of our Clients based in Paris. I am gathering a new team which will report to the Regulatory Affairs Manager of this Global company of 4000 people across Europe, the US and Asia. ...
Senior Manager Regulatory Labeling
New York
Dec 1
My client is a leading Pharma/Biotech business with operations globally and with multiple US locations. They are currently looking to secure a Senior Manager Regulatory Labeling to join the organisation here in the US.
Regional Regulatory Lead
Surrey
Dec 1
This attractive Regional Regulatory Lead job is a great opportunity to join one of the pharma industry's biggest and most prestigious organisations. The company is located in the UK and has been working for over a 150 years across multiple therapy areas including cardiovascular, neurology and immunology. This is a contract role based in Surrey, UK. ...
regulatory jobs : 100 +
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