Job Description
Regulatory Affairs Specialist
Job description:
Full time On-Site, 9:00AM to 6:00PM in Polanco CDMX, Mexico
Immediate job!
Chemist/ Biologist and also Pharmacist Diploma in order to act as sanitary responsible
Experience in Dossier preparation for Drug products: take care of the preparation of your dossier.
Printing, submitting.
Including preparations of all legal documents, translations, label artwork...
Approving and submitting Pharmaceutical dossiers to COFEPRIS.
High communication skills in English & Spanish
Experience in drug product registration at COFEPRIS
Regulatory affairs:
1) Connect between companies/manufacturer and regulatory authorities by ensuring that products are manufactured, tested, and distributed in compliance with appropriate legislation.
3) RA responsible for preparing responses to customer requests for information, reviewing clinical protocols, writing or updating standard operating procedures, work instructi...