# Having 12 years of experience in the Pharmaceutical and biopharmaceutical industry in
Quality Control department.
# Strong understanding of GMP and GLP guidelines, Regulatory requirements and compliance to the
principles of various health authorities.
# Extensive skills in GMP compliance and IT compliance.
# Successfully handled USFDA, WHO, KFDA, COFEPRIS, ISO and Customer inspections.
# Ability to implement good quality systems in working with a team-oriented setting.
# Ability to work independently on multiple task and make responsible decisions as a good
team member.
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