Global Regulatory Sciences
Job Description
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.
Candidates with relevant technical experience in Pharma R&D, Tech Transfer, Quality & Manufacturing, aspiring for Regulatory role can also apply, and will be considered based on fitness and potential.
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-PFEPfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.
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