**Duties & Responsibilities**:
1.
Perform testing for stability, semi finish good and finish good as per applied procedure
2.
Coordinate with QC FG Team Leader and QC Admin on the availability of reagent, HPLC column, reference standards, media, glassware and other materials required to support testing analysis
3.
Perform activity related with projects, such as analytical method validation, analytical method transfer, analytical testing of bulk holding time, process validation, cleaning validation, comparative dissolution, etc.
4.
Report any out of specification (OOS) found to QC Manager or QC FG Team Leader and immediately raise as well in Phenix (ILI)
5.
Report any deviation found to QC Manager or QC FG Team Leader
6.
Ensure all testing activity is documented properly in ATR and / or logbook, and comply with Good Documentation Practice
7.
Ensure all equipments are calibrated and / or qualified
8.
As per qualification, analyst may support for sampling of raw materials and primary packing materials
9.
Actively involve in continuous improvement program in his / her area
10.
Implement HSE practice in the work place as per applied HSE policy
**Knowledge, Skills & Competencies / Language**:
Technical Skill & Competencies/Language
- Basic competency in English
- Practical experience in physical and chemical analysis, experience in modern equipment and methods.
Behavioral Competencies
Core Competencies:
- Strive for result (exceed standard performance)
- Act for change (participating in change)
- Corporate transversally (leverage team work)
- Commit to customer (take responsibility to fulfill customer needs)
General Competencies:
- Continuous Learning (Practical & Actual Learning).
- Analytical Thinking (Break Down Issues).
- Committed To Org.
Ethic (Act With Integrity)
- Communication (Clear Message).
- Adm, Record, Data Handling, Planning & Organizing (Reporting & Administration Understanding).
**Qualifications**:
- Diploma in chemistry, chemical analyst, biology or pharmaceutical vocational school
- Min 1 year experience as a laboratory analyst in pharmaceutical company
- Experience in running laboratory modern equipment and testing method
- Technical Equipment Know How
**Requirements **of the job**:
- Having broad knowledge of GMP, GLP, local pharmaceutical regulations, analytical methodology and product transfer
- Having broad knowledge on pharmaceutical manufacturing process
- Basic communication skills in English
- Aptitude for transversal collaboration and teamwork
- Good knowledge on xls., word and ppt.
- Detail, process oriented and performance focus
Li-Sea
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.