Description
**Date:** Oct. 22, 2025
**Location:** TLAJOMULCO DE ZUÑIGA, 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 mark on the world!
**Type of Collaborator**
Operational**Position Objective**
Perform microbiological analyses of environmental control, facility, equipment, and personnel samples to ensure compliance with established sanitary and quality regulations, thereby contributing to the control and prevention of microbiological risks.
**Responsibilities and Activities**
1\. Prepare and analyze various types of samples (e.g., water, medications, pharmaceutical products, clinical samples, etc.) to detect pathogenic microorganisms or indicators of contamination.
2\. Ensure all procedures and microbiological analyses are conducted in accordance with the laboratory’s quality and hygiene regulations.
3\. Maintain inventory of materials and equipment, ensuring required supplies are available and within their expiration dates.
4\. Accurately record results and ensure quality control records and documents remain up to date.
5\. Operate and maintain laboratory equipment in optimal condition, performing periodic calibration as specified in quality procedures.
Experience
Microbiology laboratories in the pharmaceutical, clinical, cosmetic, or food industry (preferably in quality control areas). \- 1 Year
Environmental, equipment, and facility microbiological sampling. \- 1 Year
Knowledge
* Practical knowledge of microbiological techniques (culturing, isolation, identification, rapid tests, PCR, etc.)
* Quality Management Systems
* Knowledge of quality regulations and standards, such as Good Laboratory Practices (GLP) and Good Documentation Practices (GDP)
* Intermediate proficiency in Office software
Education
Bachelor’s degree in Pharmaceutical Chemistry and Biology or Biochemistry**Complementary Profile**
Analytical method validation
Applicable regulations (e.g., NOM-059, FEUM, etc.)
At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunity, inclusion, and diversity. Our selection processes are FREE OF CHARGE; please report any irregularities to lineaeticagrupopisa@letica.email