
Global Regulatory Sciences
7 days ago
Preferred Experience:
2-15 Years in Pharmaceutical industry with major experience in Global Regulatory Affairs function. Authoring and/or contributing line to CMC content for New Development & Post-approval Variations/ Supplements for Chemical Entities, Biologicals, Vaccines (INDs/ IMPDs/ NDAs/ BLAs/ ANDAs/ MAAs/) & Medical Devices (PMA/ 510(K)/ Notified bodies/ Design History File) for Global markets.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
LI-PFE
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