*somos visionarios, motivados para resolver los riesgos más difíciles del mundo y luchar por un mundo en el que salud para todos hambre para nadie ya no sea un sueño sino una posibilidad real.*
*lo estamos haciendo con energía, curiosidad y absoluta dedicación, aprendiendo siempre de las perspectivas únicas de quienes nos rodean, cambiando nuestro modo de pensar, ampliando nuestras capacidades y redefiniendo el concepto de «imposible».*
*hay muchísimas razones para unirse a nosotros. Pero si lo que desea es construir una carrera profesional significativa y diversa dentro de una comunidad de mentes diversas y brillantes para marcar una diferencia importante, solo hay una opción.*
*qc microbiology lead*
*your tasks & responsabilities*
1. To define and/or establish the microbiological validation and transfer methods criteria, assuring fulfillment with the gmp's requirements (ministry of health regulations and bayer regulations) guarantees compliance with current quality, analytical safety, environmental impact, and occupational hygiene standards.
2. To guarantee availability of resources (human, technology, supplies, etc.) to comply with the microbiological analysis activities in the products and areas, gmp documentation and adherence to the product delivery plan to the client.
3. Lead the staff in a collaborative environment and opportunities, developing the team to face challenges and/or new position. (successor plan, development & performance).
4. To search, evaluate and implement new practices and methods to make more efficient the work, optimizing products and areas release time.
5. Implement strategies and define kpi´s to achieve the objectives, for example: release time for raw materials and finished products, environmental monitoring, quality standards with impact to service level.
6. Promote the training of the team in relation to gmp/glp, hse, life values and job functions. Manage projects of operational excellence with the participation of the area.
7. To assure the microbiological results of stability studies, to support the expiry date and period approved by the ministry of health authorities.
8. Attend health authority inspections in the microbiology laboratory, provide adequate answers/evidence of the procedures and data generated to support the glp compliance. Lead the tour and response to recommendations/findings.
*who you are*:
- bachelor's degree/master's degree desirable in chemical pharmaceutical biology or equivalent 5 years of experience solid knowledge and understanding of process qualification, validation and development of microbiological analytical methodologies.
- management of pharmaceutical standards: european pharmacopoeia, usp, feum, among others, as well as mastery of national and international regulations on gmp/glp.
- domain of national (nom) and international (iso, ich, pic/s, fda, ema, who) regulations.
- management of national and international audits
- advanced english level
- leadership, personnel management, self-learning, decision making, confidence building, complexity and uncertainty management. Self-development, trust, decision-making, collaboration and teamwork, personal development, drive for results
*período de aplicación*:
- del 29 de julio al 12 de agosto 2025
*código de referencia*:
- 851022
*división*:
- pharmaceuticals
*ubicación*:
- mexico : veracruz : jalapa
*área funcional*:
- calidad
*grado de posición*:
- vs 1.1
*tipo de empleo*:
- permanente
*tiempo de trabajo*:
- indeterminado