Manufacturing and Supply
Wo Wunder
der Wissenschaft
für Patient*innen
Realität werden

Main responsibilities:

• The main purpose of this job is to perform chemical analysis for validation samples for products according to the approved method of analysis, and prepare relevant documentation as required.
• Perform analytical method validation/verification studies ,Protocols & final reports.
• Perform recovery studies & prepare cleaning validation & verification runs.

Responsibilities and Tasks:

1- Performs all physicochemical testing of samples collected during the process validation and record the results in the validation report & Certificates of analysis required and ensures that all obtained results are within the specified approved limit, using valid method of analysis.

2- Performs the analytical transfer analysis according to respective protocol.

3- Perform coaching and training for junior analyst for the Analytical method validation and explain the methodology and ensure that all the junior analyst (s) understand the method validation concept and can perform full study independently .

3- Immediate reporting of out of specification test results or batch deviation reports whenever needed to the Q.C manager.

4- Perform analytical full method validation studies , Protocols & final reports.

5- Updating of SOPs & control test methods and maintaining of relevant master files.

6- Performs Standardization for Raw Materials

7- Perform Stability testing & routine analysis tasks as assigned

8- Perform recovery studies & prepare cleaning validation & verification runs.

9- Fulfill other task(s) as assigned

10-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.

      ● Perform 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.

- Required Years of Experience:

3 to 6 years

Pursue Progress. Discovery Extraordinary.

Werde Teil von Sanofi und starte mit uns in eine neue Ära der Wissenschaft – wo dein persönliches Wachstum genauso wegweisend ist wie unsere Arbeit. Wir investieren in dich, damit du weiterkommst, schneller denkst und Dinge möglich machst, die vorher undenkbar waren. Du wirst Grenzen verschieben, Gewohntes hinterfragen und smarte Lösungen entwickeln, die direkt bei den Menschen ankommen, für die wir da sind. Bereit, die Wunder der Wissenschaft zu jagen und Leben zu verbessern? Dann lass uns gemeinsam Großes bewegen – und das Außergewöhnliche entdecken.

Bei Sanofi stehen allen die gleichen Chancen offen – unabhängig von Herkunft, Hautfarbe, Religion, Geschlecht, Nationalität, sexueller Orientierung, Alter, Staatsangehörigkeit, Familienstand, Behinderung, Geschlechtsidentität, Veteranenstatus oder anderen gesetzlich geschützten Merkmalen.