Bachelor Degree in Lifesciences/Pharmacy preferred
2-4 years of experience in Regulatory affairs and submission, with Corporate experience
Strong analytical and problem-solving skills
Strong written and oral communication skills
Excellent planning, coordination and Project Management skills
Experience in continuous improvement projects and quality management
Your responsibilities will include:
To assist the Publishing & Regulatory Data Entry Manager in providing Global Submission view and strategy Worldwide, in line with Regulatory Strategic Planning.
To ensure that metadata submitted to the Health Authorities (HA) and coming from HA are accurate and that Ipsen Regulatory tracking system is aligned.
To ensure that Regulatory Tracking System is appropriately maintained.
To oversight Service provider(s) for the Centralized Data Entry and HA document upload activities.
Communicates on Regulatory Data process/timeline with RA community, and contributes to the planning of the regulatory submission.
To ensure that accurate and up-to-date regulatory information on products, under development, approved and marketed, worldwide is available to all stake-holders.
A career path
A great diversity of cultures
Language courses and training
On-site relax & gym rooms