Sanofi is recruiting for QC Analyst professional
JOB PURPOSE:
The main purpose of this job is to perform routine and stability chemical analysis for products on daily basis according to the approved method of analysis.
KEY RESPONSIBILITIES AND DUTIES:
1- Performs all necessary testing procedure, issues Certificates of analysis required and ensures that all obtained results are within the specified approved limit, using valid method of analysis.
2- Review all Obtained results for semi-finished products against the Out of trend limits and all the stability Results against the BIOST@T and ensure that all results are within the normal trends
3- Immediate reporting of out of specification test results or batch deviation reports whenever needed to the Chemical lab head and the Q.C manager.
4- Sampling of semi-finished products, and ensures that sampling are conducting in full compliance with GLP and according to the instructions as per the SOP.
5- Perform Stability testing & assigned validation analysis tasks
6- Perform Printed packaging testing.
7- Fulfill other task(s) as assigned
8- HSE & Energy Contribution:
Ensures HSE approval on any SOP that requires certain HSE precautions. Ensures HSE approval on any change. Follow the laboratory safety procedures 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. Implement good calibration program for all instruments.
Supplementary Tasks:
Utilizes, calibrates, maintains the QC equipment in the Chemical Lab according to the local SOP.
Prepares relevant SOPs and follows up the update according to requirements.
Performs other related duties as assigned.
Makes sure that all activities carried on are complying with safety measurements.
Updates methods of analysis.
Respect of Company’s Values, Code of Ethics and Social Charter.
Responsible for applying the HSE related requirements for the company in all working procedures
Respect Personal Data Protection Charter.
Administration tasks in case of absence of the senior Administration Officer:
Receiving of Materials receipt records delivered from the warehouse for all batches of Raw, Aux, Primary packaging, & Printed packaging, , and recording them in Q.C samples receipt record, and delivers them to Q.C samplers to start sampling and analysis processes
Receiving of Analysis Demands delivered from the production areas for all manufactured batches of semi-finished products, and recording them in Q.C samples receipt record, and delivers them to Q.C samplers to start sampling and analysis processes
Checking of the Received printed packaging materials under the supervision of the Material and packaging material section head.
Responsible of preparation and adequate arrangement of all Q.C filling system and ensure correct and easy retrieval of any requested record and / or document.
JOB REQUIREMENTS:
6 months - 2 years experience in related positions, preferably in multinational company.
command of English Language
Good computer skills / MS
Familiar with new instrumental analysis techniques
HSE appropriate knowledge
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.
