Fabrication et Approvisionnement
Là où les miracles
de la science
deviennent une réalité pour les patients

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

About the Job:

Job Responsibilities:

• Deviation Investigations:

  • All deviations in the process or specifications that can affect product quality are investigated to evaluate the root cause, corrective actions and preventive measures needed to prevent re-occurrence.

  • Ensure of non-recurrence of repeated deviations.

• Shopfloor Activities:

  • Review of the batch records before release to the market.

  • Manage batch record archiving

  • Performing quality tours in each manufacturing GMP area.

  • Maintain compliance to local and Sanofi regulations in manufacturing areas.

  • Execution APR plan execution

  • Manage Quality culture program of the site.

  • Monitor Data integrity program of the site.

  • Monitor deviations impacted non-sterile areas.

• Finished goods disposition. -

  • Collecting data daily from the various departments concerned i.e. production, packaging, &     Q.C

  • Checking and reviewing the data to ensure its adherence to specified protocol & therefore, according to Sanofi   Directives & Guidelines & current GMP, on daily basis.  

  • Checking the finished goods retain samples.

  • Following up corrections with the concerned person in the respective department.

  • Summarizing data from protocols through documenting them in standard checklist& batch release.

  • Archiving of batch records with its concerned attachments up to 10 years.          

  • Delegated by QA manager for finished products release/reject activities for non-sterile / sterile batches.

• Quality tours

  • Perform routine Quality tours in the responsible areas.

  • Perform GEMBA & process observation within the responsible areas.

• HSE Responsibilities:

  • Ensures HSE approval on any SOP that requires certain HSE precautions.

  • Ensures HSE approval on any change.

  • Commitment to the appropriate PPE use.

  • Follow the approved HSE policy and requirements.

  • Following the statutory legislation concerning Health, Safety and environmental law.

  • Hydrocarbons/ hazardous substance & waste segregation in accordance with approved waste management system.

JOB-HOLDER’s ENTRY REQUIREMENTS:

• Bachelor’s degree in pharmaceutical science

• 3-5 years of related experience

• Shop floor activities.

• QA Documentation and compliance systems experience.

• Expert in Pharmaceutical industry & raw materials “API & Non-API”

• Decision making & problem solving.

• Deviation management

• Risk management & Root cause analysis tools.

Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.