Description
Job Summary:
Supervise and manage staff activities related to the established quality system and perform duties as an assistant to the Regulatory Affairs Responsible Person.
Key Highlights:
1. Committed to the health and well-being of millions of people.
2. Be part of a company striving to transform the future of healthcare.
3. Promote equal opportunities, inclusion, and diversity.
**Date:** Mar 18, 2026
**Address:** Carr. a San Isidro Mazatepec 7, JALISCO, MX
**Company:** Grupo PiSA
Live your purpose and make a difference with Grupo PiSA.
With over 80 years of history, Grupo PiSA is a 100% Mexican company committed to the health and well-being of millions of people, both in Mexico and internationally. Our growth reflects the effort, passion, and dedication of a team focused on excellence.
Join us and become part of a company where every day is an opportunity to live "A Life in Service of Life".
Together, we can transform the future of healthcare and leave a positive impact on the world!
**Employee Type**
Trust-based
**Job Objective**
Supervise and manage the activities of assigned personnel related to the established quality system and perform duties as an assistant to the Regulatory Affairs Responsible Person.
**Responsibilities and Activities**
* Coordination and verification of processes and installation of the finished product warehouse.
* Identification, handling, and control of deviations from GMPs (including non-conforming products) in the finished product warehouse; risk management applicable to storage and distribution; audit findings; follow-up on complaints; and evaluation in case of any process changes.
* Verification of stock levels for blocked products and handling of market withdrawals, including release when applicable.
* Supervision and control of controlled medications handling.
* Training of assigned personnel and updating of area documentation.
Experience
* Mexican Pharmaceutical Regulations: 1 year
* Attribute Inspection: 6 months
Knowledge
* Quality Management Systems.
Education
Bachelor's Degree
**Complementary Profile**
EXPERIENCE:
* Handling of controlled products
* Quality or Quality Assurance area
* Pharmaceutical industry
KNOWLEDGE:
* Audits
* Basic Excel (basic operations, data filtering, etc.)
* ISO\-9001 Standard
* ERP System (SAP)
At Grupo PiSA, we prohibit violence and discrimination and promote equal opportunities, inclusion, and diversity. Our selection processes are FREE OF CHARGE; report any irregularity at lineaeticagrupopisa@letica.email