poland, Poland
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Applicants:3
Posted on 3 Jun, 2025
Manage eCTD submissions, publishing globally.
Ensure compliance with HA standards (US, EU, etc.).
Collaborate across global, cross-functional teams.
Support tools, process improvements, and issue resolution.
BSc Life Sciences, pharma experience.
eCTD & regulatory knowledge (FDA, EMA, ICH).
Works independently and in teams.