A
Ashish Life Science
Formulation And Development - Research Associate
1 month ago
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Important information
Contract type:
Permanent
Location:
Ambernath, Maharashtra, India
Work mode:
Onsite
Published on:
16 September 2026
What they need
- 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 Good 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
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