- Batch filling related activity for all products of PFS/Vial/Cartridge and PFS-Cartridge nested filling machine.
- Execution of finished product filling activity as per SOP.
- Issuance of RM/CM/PM. Supervision, preparation and filtration of disinfectant solution.
- Check and prepare documentation related to manufacturing, autoclave and filling activity.
- Fill / verify / check and sign as a production chemist in GMP document
- Responsible for proper maintenance and sanitation in FP and its associated area.
- Operation and cleaning of LAF, Energetic passbox, Glove integrity tester.
- Activities other than mentioned above after completion of Training.
- To follow Good Documentation Practices and Data Integrity’ requirements during any GxP Operation and recording at site.
- To take responsibility that application of Data Integrity requirements and potential consequences for not following it are understood and followed.
- To review in the perspective of compliance to Data Integrity requirements while reviewing any GxP data (Records, Reports) specific to .
- To ensure that, In case of any event of potential data breach, it shall be handled through SOP on ‘Handling of Potential Data Integrity Observation.