Quality Analyst I

Sé de los primeros solicitantes.

Teva Pharmaceuticals

Estado de México

MXN 200,000 - 400,000

Sé de los primeros solicitantes.

Hace 4 días

Descripción del empleo

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Quality Analyst I

Date: Dec 16, 2024

Location: Estado de México, Mexico, 00000

Company: Teva Pharmaceuticals

Job Id: 59741

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

This section is where we attract the attention of potential candidates and sell the role. How has the role come about? What makes it appealing? What are the key responsibilities? How is the role better with Teva than with another company? Wherever possible, we should bring through the essence of our EVP pillars, i.e., we care, we’re in it together, and we make work fulfilling.

Your experience and qualifications

Educación: Carrera en Química, Químico Farmacéutico o escolaridad equivalente
Experiencia: 4 años de experiencia en el área de validación
Capacidades: Conocimiento y manejo de GMP´s, Normas y regulaciones nacionales e internacionales, Buenas Prácticas de Documentación, validación de procesos, sistemas críticos, limpieza, calificación de equipos y sistemas computacionales
Ingles: intermedio

Emitir el Plan Maestro de Validación y sus programas de actividades relacionados.
Asegurar la ejecución del Plan Maestro de Validación para los diferentes procesos, sistemas y equipos, dando cumplimiento al mismo.
Asegurar que los equipos mayores o críticos que se usan en el proceso de manufactura son calificados en DQ, IQ, OQ y PQ según sea el caso.
Asegurar que el proceso de manufactura se encuentra calificado de acuerdo a regulaciones aplicables.
Asegurar que la limpieza de los procesos es adecuada, mediante la validación de la misma en las diferentes etapas del proceso de manufactura.
Apoyar con la información requerida por otras áreas referentes a la validación de procesos.

Reports To

In process of validation

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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