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Open nowPosted yesterday

Operador

Sanofi1,017 open roles

Where
Ocoyoacac
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Your applicationOpen nowOperadorSanofi · Ocoyoacac

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Sanofi's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

13.5% of postings close within 7 days. Measured by our own scanner across the market. Sanofi postings stay open a median of 14 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.6%3 days
  3. 13.5%7 days
  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted yesterday

Sanofi median: 14 days open

The posting

QU-REC-0932236-Descriptivo de puesto de operador A de purificación, downstream septiembre 2025.

Responsabilidades:

✓ Realizar las actividades de producción con el área de Clarificación para la repartición de las fracciones a ser

recibidas en la etapa 9 del proceso de producción del granel de antígeno monovalente contra influenza.

✓ Realizar el arranque, limpieza y operación de los equipos utilizados en las etapas 9 a la 14 del proceso de

producción tales como ultracentrifugas Alfawassermann KII y centrifugas Beckman Óptima, refractómetros,

bombas peristálticas, Sartocheck, autoclaves, MAS 100, Climet y campanas de flujo laminar de acuerdo con lo

establecido en los procedimientos de operación y limpieza específicos para cada equipo, siguiendo en cada uno

los lineamientos de calidad y seguridad aplicables.

✓ Realizar el monitoreo de partículas viables y no viables, CAP, N2, toma de agua, siguiendo lo establecido en los

Procedimientos vigentes, para el cumplimiento de la fabricación del granel antígeno monovalente contra la

influenza con Calidad.

✓ Realizar los registros (Procedimientos de fabricación, registros en bitácoras, identificaciones de área,

identificaciones de materiales y producto) generados por el proceso de Purificación de acuerdo con los atributos

de calidad ALCOA (Atribuible, Legible, Contemporáneo, Original, Acertado) para los registros GMP.

✓ Solicitar el material necesario para trabajar en tiempo (material, soluciones, insumos para limpieza y proceso).

✓ Seguimiento, actualización y cumplimiento la % de capacitación requerido de acuerdo con la matriz general de

capacitación (cumplimiento de capacitaciones por iLearn).

✓ Mantener activos sus accesos electrónicos (Windows, SAP, Adobesing, Master, así como, los accesos a los

equipos que utilizan en sus áreas de trabajo.

✓ Uso responsable de instalaciones, equipos, equipo de protección personal y herramientas.

✓ Seguimiento a los estándares SMS 2.0 (+QDCI, manejo de ayudas visuales, estandarización de trabajo, robustez

de proceso, mejora continua, cuidado de equipos).

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

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  2. 25 readers review it

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    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on Sanofi's form

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