Your role will ensure Pfizer maintains compliance by delivering the portfolio of one or multiple applicable regulatory obligations
Job Summary
Your role will ensure Pfizer maintains compliance by delivering the portfolio of one or multiple applicable regulatory obligations.
Supports delivery of electronic and paper regulatory transactions and electronic review aids in support of Drug Listings, Drug Establishment Registrations, certificates and samples sourcing, XEVMPD submissions and other post market scheduled regulatory compliance activities in accordance with 21CFR 314.81.
Contributes to the completion of moderately complex projects.
Matching Summary
Your role will ensure Pfizer maintains compliance by delivering the portfolio of one or multiple applicable regulatory obligations.
Skills & Requirements
Must-have
electronic and paper regulatory transactions
post market scheduled regulatory compliance
Drug listing and Establishment registrations
electronic technologies for submissions
relevant regulatory industry knowledge
Nice-to-have
innovative thinking
meticulous attention to detail
strong analytical and problem-solving skills
ability to work independently and as part of a team
Key Requirements
2+ years of experience
understanding of applicable filing regulatory guidelines
knowledge of drug development process
familiarity with systems and electronic technologies