Indefinido
Shanghai Shi
Shanghai
Investigación
Jornada Completa
14-Feb-2023


For more than hundred years, L’Oréal believes that beauty needs Science. In a world now transformed by digital technology and the emergence of new scientific domains, we are confident in our ability to turn these opportunities into major innovations, closely linked to the new consumer expectations all over the world. Science & Technology are allowing us to invent safe, trustable, sustainable & responsible beauty products and experiences that will change people’s lives. 

L’Oréal Research & Innovation (R&I) has continuously invested upstream in its research with a high level of ambition. Our 4 100 L'Oréal R&I people are talented and highly skilled, located in major markets, working in a cooperative way, open to the world.

In the department of SRCM, we are looking for an Expert. 

 As an Expert, your main responsibilities are: 
  • Implement the strategy related to regulatory / safety / claims aspects in order to ensure the application of regulations in force in the target countries for the development, marketing and distribution of medical deviceProvide an interface with Asia Pacific and Americas Hubs on regulatory / safety / claims aspects for medical device project development.
  • Participate in the regulatory / safety / claims evaluation of medical device acquisition or licensing projects
  • In case of Legal Manufacturer liability, and in close collaboration with internal or external partners, coordinate and plan the elaboration plan of the parts of the CE marking file as well as the answers to the questions of the notified bodies for obtaining and maintaining the CE marking
  • In case of Distributor liability, contribute to the elaboration of quality contracts with the external partner
  • Advise and assist the departments concerned (Research & Innovation, Industrial Operations, Legal, Marketing, Finance, etc.) on regulatory / safety / claims aspects
  • Verify and validate medical device instruction manuals and labeling
  • In close collaboration with the Regulatory Intelligence department, monitor and analyze regulatory developments worldwide and perform impact analysis on medical device projects under development or to be developed 

To succeed in this position, you have: 
  • Education background
  • Required professional experience
  • Mandatory technical skills and Nice to have technical skills
  • Fluent in English

You are : 
  • More than 10 years of experience in Project management of medical devices for regulatory / safety / claims aspects 
  • Bac+5/ Master's degree: a degree in pharmacy, medicine or engineering with a specialization in regulatory affairs in the field of medical devices
  • Your pragmatism, your autonomy, as well as your ability to analyze and synthesize will be assets that you will use daily to carry out your missions successfully
  • Ability to work in a transversal and multidisciplinary way
  • Ability to be a development partner looking for agile and innovative solutions; very good interpersonal skills 
  • Ability to anticipate and plan ahead
  • Fluent in English and French
  • Writing skills: rigor, semantics, synthesis and analysis
  •   

If you identify yourself in this position, please apply by uploading your resume in PDF

The L'Oréal Group is convinced that difference is a deep source of wealth, that allows everyone to grow, to challenge themselves and to go further. We strongly encourage everyone to always dare and never censor themselves. Skills can always be learnt. We will be delighted to exchange with you! 


To discover our scientific and technical functions at l'Oréal Research & Innovation, please check our career website : https://careers.loreal.com/en_US/content/ResearchInnovations?3_4_3=128 

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