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 Purpose:

Non-Sterile Production pharmacist in IPC department which responsible to ensure all products, in process materials, production facilities and process comply with the Company’s Quality Management standards and Government’s cGMP requirements through proper monitoring procedures, effective training program and up-to-date documentations

KEY RESPONSIBILITIES AND DUTIES:

1-    Management of In-process control Process:
a.    Supervising operators during the in-process control, assuring the process flow according to GMP rules & monitor their capability, performance & enhance it through training & motivation.
b.    Check the recording in the IPC devices logbooks daily.
c.    Check the calibration & cleaning of IPC devices to ensure compliance with GMP standards & guidelines Assuring the validity of measuring and controlling devices (balances, IPC Instruments)
d.    Report deviations related to process and participated in the investigation as relevant and ensure optimum communication with Production team and QA team.
e.    Prepare & implement plans for technical training of both newly hired & existing staff to enhance performance especially in areas of GMP concepts, HSE & SOP system. 

2-    IPC Documentation Management: 
a.    Updating / creating SOPs & supervise implementation of SOPs by all workers.
b.    Creating / Updating Logbooks .

3-    Calibration / Qualification Plan.
a.    Prepare the yearly calibration / qualification plan for IPC Equipment.
b.    Perform the calibration and Qualification activities in house as relevant.
c.    Follow up the implementation and organization with local calibration team / external suppliers for on time calibration / Qualification of IPC Equipment.

4-    IPC Capex: 
a.    Assess the need for CAPEX for IPC department based on the long-term plan to ensure the availability of needed Equipment for testing.
b.    Prepare URS / Get offers follow the purchase of equipment till delivery and qualification.

5-    Make annual plan for providing the department with process consumables (labels, stationary tools ...etc.) and perform the role required in the procurement process. 

6-    SMS Activities:
a.    plan for the process improvement such as increasing productivity, capacity, optimizing use of resources etc. 
b.    Share in the lean and other industrial activities.

7-    Tablet compression sets Management:
a.    Ensure there is a system for management of tablets compression machine punches and dies, including recording of use in logbooks and inspection before and after use.
b.    Ensure there is a process for periodic checking of punches to identify the need for repair / or Replacement and ensued the optimum usage and lifetime.

8-    Working as Second Line for Solids and manufacturing areas and Dispensing Area 

9-    Responsible of Procurement activities through managing all OPEX & CAPEX for NS-production unit.

HSE & Energy Role:
1.    Applying the machine safety checklist on regular basis.
2.    Ergonomics training on regular basis.
3.    Commitment to the appropriate PPE use
4.    Ensures that risk assessment to any new transferred product and new machine is adequately covered.
5.    Continuous monitoring to the first aid boxes 
6.    Executing waste management measures for optimum utilization of resources.
7.    Follow the approved HSE policy and requirements.
8.    Follow all the statutory legalization concerning Health, Safety and environmental law.

About you :

Education: Bachelors' degree of Pharmacy

Related Experience: 0-2 years of experience.

Languages: Very Good written and spoken English

.

Skills & Competencies

• Strong communication, time management, and analytical skills.
• Ability to work under stress and in teams.
• Proactive, detail-oriented, and committed to continuous improvement.
• Leadership and strategic thinking capabilities.
• Good Manufacturing Practices (GMP) & Good Documentation Practices (GDP).
• Good command of Microsoft office

Take The Lead Values:

• Aim Higher: Focus on what matters, set high standards and move with urgency, learning from setbacks as we go to achieve higher performance.

• Act for patients: Never compromise on integrity, eliminate barriers, and partner with others to go faster and further for patients.

• Be Bold: Take thoughtful risks, seize opportunities and think beyond what’s possible to accelerate our science and drive compelling growth.

• Lead Together: Build trust and collaborate openly on our shared goals, celebrate collective wins and foster a sense of belonging. 

Why choose us?

• Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.

• Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale.

• Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

• Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.

• Work with AI, robotics, and next-gen automation to redefine global manufacturing and supply.

• Be part of world-first initiatives like our Modulus factory, smart factories, and AI-driven supply chain solutions.

• Help deliver 30+ new product launches by 2030, ensuring patients get treatments faster than ever.

• Develop new skills, explore cross-functional roles, and work in an environment that values growth and discovery.

• Every year, we distribute over 4 billion units of medicines and vaccines, ensuring people worldwide receive the treatments they trust.

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.