- RM and PM receiving and documentation of the same.

- Proper arrangement of the Received COA of RM and PM.

- Sampling of Received RM and PM, sending the samples to ADL for analysis.

- Preparation of indent for trial activity and ensure the availability in defined time.

- Taking of daily trial batches, discussion of issue with immediate supervisor.

- Entry of trial batch data in lab notebook and preparation of BMR for stability batches.

- Maintaining the files of individual products like RM and PM COA, Trial COA and Stability Reports after updating in Excel Sheet.

- Ensure GMP practice in Laboratory routinely.

- Documentation of stability batches.

- Calibration of instruments in the laboratory.

- Literature search and review for the newly identified products for EU/UK/Raw market.

- SOP preparation and submission to DQA.

- Ensure utility in good condition in laboratory during all development batches.

- Adhere Good Manufacturing Practice and Positive Laboratory Practice throughout lifecycle of the product.

- Technically sound in development of Injectable/ Oral solid products and semisolid and liquid dosage forms.

- If additional knowledge of regulatory documents preparation is essential

📌 Formulation And Development - Research Associate (Ambernath)
🏢 Ashish Life Science
📍 Ambernath