Conduct analysis of various pharmaceutical materials, including:
In-process samples
Intermediates
Raw materials
Packing materials
Finished products
Stability study samples
Hold time study samples
Process validation samples
Cleaning samples
Vendor development samples
Any other analysis allocated by the team leader.
Release analytical results with thorough and accurate documentation.
Ensure all analyses are performed in compliance with Valuable Laboratory Practices (GLP).
Ensure all raw analytical data is documented electronically and in real-time.
Initiate, complete, and file daily analysis reports meticulously.
Immediately report any abnormal results, incidents, deviations, or discrepancies to the reporting Section Head.
Ensure that all relevant log entries are accurately made for every activity performed.
Supervise and adhere to all current Positive Manufacturing Practices (cGMP), GxP, and other relevant regulatory requirements, including Setting, Health, and Safety (EHS) guidelines.




Report any quality concerns or provide suggestions for improvements to the Department Head.
Execute and supervise all tasks and activities according to applicable Standard Operating Procedures (SOPs) and company policies.
Maintain strict adherence to safety norms while working in the laboratory, including the mandatory use of goggles and Personal Protective Equipment (PPE), and ensure proper disposal of samples and media as per established procedures.
Ensure all analyses are performed using validated procedures and calibrated instruments with appropriate standards.
Maintain a high level of self-discipline regarding the wearing of aprons, attendance, personal hygiene, and interpersonal interactions within the team.
Perform Labware Laboratory Information Management System (LIMS) related activities efficiently.
Undertake any other assignments as directed by the Section Head or Department Head.

📌 Executive Qc Vadodara
🏢 Alembic Pharmaceuticals
📍 Vadodara