Role & responsibilities

- To perform all test for in process product & finish product as per the specification and schedule.
- To investigate failure of FP / Out of specifications (OOS) and take the corrective and preventive actions (CAPA).
- To perform and ensure the calibration of instruments as per the schedule.
- To perform and ensure preparation of reagent / volumetric solution as per schedule.
- To perform and ensure observation of FP retained samples.
- To ensure that all documents related to the testing data and related papers are maintained properly.
- To implement Corrective and Preventive Action (CAPA).
- To carry out the sampling of all the materials according to Standard Operating Procedure (SOP).
- To carry out the testing of Raw Material and Packing Material according to approved procedure.
- To release Raw Material and Packing Material.
- To carry out the calibration of instruments as per the schedule.




- To prepare the working standards as per the guidelines and various pharmacopoeias.
- To ensure the status tag on the released material and transfer such material in the released area.
- To follow the Good Laboratory practices and Valuable Manufacturing practices (GMP).
- To prepare requirement list of chemical & reagent for procurement.
- To perform the analysis of stability sample as per current specification.
- To compile the data required for internal quality audit in the plant, as and when required.

Preferred candidate profile

- Managerial skill
- Problem solving & Decision Making skill
- Guiding skill
- Team development skill
- System thinking
- Delegation

Interested candidates can share their CV at [HIDDEN TEXT]

Fresher can also can apply and their CV on the mentioned email ID

📌 Process Incharge -QC ( RM / PM & IPPT / FP ) (Ahmedabad)
🏢 Otsuka Pharmaceutical India
📍 Ahmedabad