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Quality Consultant
Il y a 2 mois
At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers.
Indegene is looking for a France-based Consultant with Regulatory or Compliance or Nominated Signatory Review experience for Medical Devices promotional and scientific communication materials on 3-4 months contract starting October 2024. The regulatory consultant will work with Indegene’s material review team to support its engagement with the medical device client partner and serve as a consultant to assist as an MLR SME (especially on medical device promotion regulations) on a medical device project.
We provide comprehensive medical, regulatory, and editorial review services as well as operations support through a team of 350+ experienced professionals. As a Medical Device Consultant for Regulatory or Compliance or Nominated Signatory Review of Promotional and Scientific Communication Materials , you will be responsible for providing expert France Medical Device Promotion related Regulatory advice to the Indegene team with direct or indirect involvement in the client project, ensuring the client project requirements are met.
Provide guidance on standards pertaining to advertising and promotion of medical devices in the France (and if possible, in EU and global regions).
Provide guidance on France Regulatory Requirements for promotional material review for medical devices
Provide guidance on review workflow for medical device promotional materials for France market
Provide strategic input and guidance on regulatory affairs matters, including understanding the collaboration between global and local markets for medical device promotional materials and associated review workflow for repurposing content, understanding regulatory submission guidelines, filing, negotiations, and amendments, which includes obtaining, assessing and summarizing scientific and other technical information specific for France market.
Life science graduate/post-graduate
Regulatory Affairs/Compliance professional with experience in Medical Device regulations and standards for device promotion and scientific communication, with 2 years’ experience in review and approval of medical device promotional and non-promotional materials.
Strong foundation in medical device regulatory affairs, with a total of 2-3 years working with a range of medical devices (Class 2 and above is preferred)
Has experience with and understands Germany, EU and global medical device regulations
NOTE: Please upload CV in English.
