Publicada el Publicado hace 23 hr horas
Misión del puesto
job overview
ensure that finished products comply with quality specifications and regulatory requirements by overseeing inspection, release, and shipping processes, as well as managing documentation and returned products.
main responsibilities
- ensure good manufacturing practices (gmp) in inspection and receiving areas.
- audit and release finished product shipments.
- coordinate and manage retention and analysis samples.
- follow up on customer complaints and returns.
- issue certificates of compliance and maintain records per procedures.
- enforce safety, health, and environmental policies.
- act as an internal instructor and support the improvement of the integrated management system.
qualifications
- bachelor's degree completed.
- 1 to 3 years in quality management systems, preferably in warehouses or the pharmaceutical industry.
- english – advanced level (mastery in written and verbal communication).
- knowledge of applicable pharmaceutical quality systems (nom-241, nom-059), iso regulations, sap (desirable), quality tools and aqls.
- attention to detail, teamwork, data analysis, assertive communication, resilience, decision‑making, among others.
- availability for national and international travel.
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