TRABAJO STAGE DOCUMENTATION ISO TIJUANA, BAJA CALIFORNIA

It would be a plus if you also possess previous experience in: good manufacturing practices, iso quality systems, and fda regulations writing routine reports and...

Ensure accurate and comprehensive documentation of quality processes, audits, and corrective actions... lead the development and maintenance of quality management...

Generate engineering documentation to support validations and engineering change... document all processes according to the iso quality system and fda respond opportunely...

Understand gmp and iso requirements related to manufacturing and quality... participate in product and process design reviews and stage reviews...

Serves as an internal auditor and supports external audits performs other duties in line with business needs qualifications 2-4 years qa complaint handling experience...