Role at a glance
- Job function
-
Healthcare Pharmacy & Pharmacy Support
- Salary
- Not Disclosed
- Location
- Cairo
- Work arrangement
- On-site
- Employment
- Full-time
- Experience
- Years of Experience : 3-5 years
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Role Summary
The role supervises day-to-day production activities in the liquid area, ensuring implementation of cGMP and HSE rules and fulfillment of the production plan. It supports manufacturing operations through operator coaching, validation and new projects, quality coordination, and production documentation.
What You'll Do
- Supervise operators during liquid-area production and assure process flow according to cGMP rules.
- Coach pharmacists and supervisors and train new operators on different operations.
- Coordinate calibration and preventive maintenance activities with the Quality team and engineering.
- Support new projects and validation processes.
- Update and create SOPs, report manufacturing deviations, and review batch manufacturing records.
- Monitor environmental conditions and ensure cleaning, disinfection, and machine, utensil, and room clearance according to approved SOPs.
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Original job description
Content provided by the employer
Original job description
Content provided by the employer
Job Purpose:
* Supervise day to day activities of the production process in the liquid Area with ensuring strict implementation of the GMP & HSE rules and fulfill the production plan
1. Supervising operators in liquid Area during the production process, assuring the process flow according to cGMP rules.
2. Coaching of the pharmacists and Supervisors
3. Responsible for new projects and Validation processes
4. Aligning with Quality team and engineering all the calibration and preventive maintenance activities in liquid Area
5. Ensure implementation of measures for fulfillment of liquids department weekly production plan.
6. Prevention of mix-up and cross contamination during manufacturing processes.
7. Updating / Creating SOPs.
8. Reporting any deviation occurring during manufacturing processes.
9. Training new operators on different operations.
10. Collection and Review of the batch manufacturing records.
11. Reporting any problems in utilities /machines during the production process
12. Assuring complied environmental monitoring to start manufacturing (differential pressures, temperature, and humidity) during the process.
13. Check cleaning, disinfecting and clearance of machines, utensils and rooms according to SOPs approved by the Quality Assurance Department.
14. Respect of company values, code of ethics and Social charter.
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
Years of Experience : 3-5 years
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About the company
Sanofi
Large Enterprise
Sanofi is a global healthcare leader committed to promoting health and well-being through the development of innovative medicines, vaccines, and therapeutic solutions. With a diverse portfolio that spans multiple therapeutic areas, including diabetes, oncology, and immunology, Sanofi is dedicated to addressing pressing health challenges and improving patient outcomes worldwide. Headquartered in France, the company employs over 100,000 individuals across more than 100 countries, fostering a culture of collaboration and scientific excellence to drive advancements in healthcare.