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Production Pharmacist – Oral Solid Dosage

Sanofi · Le Caire

Junior 🇬🇧 English
cGMP environmental monitoring

Job description

About the role

Sanofi is seeking a Production Pharmacist to lead the Oral Solid Dosage (OSD) area in its manufacturing facility. You will ensure that production processes comply with cGMP standards while supporting the delivery of high‑quality pharmaceutical products.

Key responsibilities

  • Supervise OSD operators and guarantee adherence to cGMP rules throughout the production cycle.
  • Implement the weekly OSD production plan and prevent mix‑ups or cross‑contamination.
  • Create, update, and enforce SOPs; report any deviations or equipment issues.
  • Train new operators on specific manufacturing tasks.
  • Collect, review, and validate batch manufacturing records.
  • Verify environmental monitoring parameters (differential pressure, temperature, humidity) before and during production.
  • Inspect cleaning, disinfection, and clearance of machines, utensils, and rooms according to QA‑approved SOPs.
  • Lead HSE activities: communicate policy, ensure statutory compliance, manage emergency procedures, conduct risk assessments, and oversee waste‑management practices.

Required profile

  • Bachelor’s degree in Pharmacy.
  • 1–2 years of experience in pharmaceutical manufacturing, preferably in a similar role.
  • Very good written and spoken English.
  • Strong communication, presentation, and project‑management mindset.
  • Ability to solve problems under pressure and adapt quickly to changing priorities.

Required skills

  • cGMP compliance.
  • SOP development and maintenance.
  • Batch record review.
  • Environmental monitoring (pressure, temperature, humidity).
  • HSE implementation and risk assessment.

What we offer

  • Opportunity to work in a leading global biopharma company.
  • Professional development in a high‑impact manufacturing environment.

Questions fréquentes

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Published 2 months ago

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Sanofi

Le Caire