This is a challenging position in the plant which gives the opportunity to be responsible for organizing the production sequences to convert raw materials into healthy semi-finished product until it is ready to be delivered to the end user in the perfect form with high quality.
Responsibilities and Tasks:
Participate in the GAP analysis of EU GMP Annex 1 Take the lead in implementation of the action plan resulting from the GAP analysis of EU GMP Annex 1 in the sterile production section Supervising Operators during the production process assuring the process flow according to cGMP rules. Updating / Creating SOPs. Training New Operators on different Operations. Collection and Review of the Batch manufacturing records. Reporting any problems in utilities /machines during the production process Ensure that SANOFI products are complying to the quality measures and standards Follow up the area performance and put action plans for its improvement Respect of companies values code of ethics and Social charter.
HSE and Energy Role:
Update the workplace RA before implementation of any change in the area Implementation of the workplace RA action plan Checking the machine safety on regular basis. Commitment to the appropriate PPE use Perform HSE awareness sections on regular basis.
Job Holder Entry Requirements:
Education: Bachelor Degree in Pharmacy
Related Experience: 0 - 2 years
Good command of English Language
Good computer skills
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues patients and customers. We respect and celebrate the diversity of our people their backgrounds and experiences and provide equal opportunity for all. apply from here