Regulatory Affairs Specialist IVD Jobs in France

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Senior Regulatory Affairs Associate France Local R...

Parexel

profile Paris - France

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

2 days ago
Full Time

Cosmetic Regulatory Affairs Manager

Lesaffre

profile Marcq-en-Baroeul - France

As part of the development of our cosmetic activity we are looking for a Regulatory Affairs Manager in Cosmetics. Reporting to the Cosmetic Business Development Director your mission will be to define plan and execute strategic projects. Working in collaboration with various departments you will con...

19 days ago
Full Time

Compliance Officer

Powens

profile Paris - France

A pioneer and market leader in Embedded Banking Powens Group is committed to supporting financial players in designing services and payment experiences that users love.Headquartered in Barcelona and Paris Powens Group is at the forefront of the Banking-as-a-Service and Open Finance movements in Euro...

25 days ago
Full Time

Manager, Regulatory Affairs

Iqvia

profile Paris - France

About IQVIAIQVIA is a global leader in healthcare intelligence committed to defining and delivering the future of healthcare. Our brand stands for innovation integrity and impactconnecting data technology and expertise to improve outcomes for patients and partners worldwide. We foster a culture of c...

30+ days ago
Full Time

Senior Regulatory Affairs Program Manager (korean ...

Sonio

profile Paris - France

About SonioEach year 140M children are born. Birth defects affect 1 in 33 births in developed countries and in 50% of cases they are not detected during prenatal examinations. Prenatal medicine is particularly complex and the scans impose heavy responsibilities on healthcare professionals. They can...

30+ days ago
Full Time

Stage Rédacteur Règlementaire Cmc (fh)

Vetoquinol

profile Magny-Vernois - France

Rattaché(e) au manager des dossiers pharmaceutiques au sein de la Direction industrielle et Qualité vous participez activement à la gestion du cycle de vie des produits de lentreprise. Dans ce cadre vos principales missions seront les suivantes :Participer à la mise en place de la stratégie règlemen...

30+ days ago
Full Time

Information Security Director

Alstom

profile Saint-Ouen - France

Req ID:505192At Alstom we understand transport networks and what moves people. From high-speed trains metros monorails and trams to turnkey systems services infrastructure signalling and digital mobility we offer our diverse customers the broadest portfolio in the industry. Every day more than 80 00...

30+ days ago
Full Time

Regulatory Affairs Manager

Bristol Myers Squibb

profile Rueil-Malmaison - France

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

30+ days ago
Full Time

Manager, Regulatory Affairs

Bristol Myers Squibb

profile Rueil-Malmaison - France

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

30+ days ago
Full Time

Manager, Regulatory Affairs

Bristol Myers Squibb

profile Rueil-Malmaison - France

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

30+ days ago
Full Time