- You will work closely with cross-functional teams to navigate the complex regulatory landscape and ensure that products meet all applicable regulations and standards.
- Prepare and submit regulatory submissions, including Investigational New Drug (IND), New Drug Application (NDA), 510(k), Pre-Market Approval (PMA), or other regulatory filings as required.
- Bachelor's degree in a scientific or healthcare-related field; advanced degree Master's or PhD) preferred.
- Minimum of 10 years of experience in Regulatory Affairs within the Pharmaceutical, Medical Device, or Healthcare industry.
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Expert Compliance Specialist - Lyon - beBeeRegulatory
Intitulé du poste: Regulatory affair manager – english/ french
Description
Regulatory Affairs Expert
This is an exciting opportunity to lead regulatory strategies and ensure compliance with global regulations for pharmaceutical, medical device, or healthcare products.
Required Skills & Qualifications
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