Job Description
Functions as GRS-CMC to assess/assist Global Regulatory Leads (GRLs) to define the Global Regulatory submission strategy and ensure timely and quality regulatory submissions pertaining to Post Approval Changes, Original Application/ Global Expansion and License Maintenance of new/ on-market Biosimilar product(s)/Biologics Product(s), Small molecule products. On market includes supporting manufacturing plants and compliance issue management.
Work Location Assignment: On Premise
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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