Key Responsibilities:
Follow cGMP, GDP, EHS, hygiene, and safety procedures in the production area.
Perform in-process, finished product, and validation sample collection as per SOPs.
Ensure proper sample identification, labeling, sealing, and transfer to QC.
Support scrap segregation, disposal, and documentation activities.
Assist in Process Qualification (PQ), Process Validation (PV), Cleaning Validation (CV), and Equipment Qualification (IQ/OQ).
Maintain production records and ensure data integrity.
Follow 5S practices and maintain housekeeping in the production area.
Use MS Office (Word, Excel, PowerPoint) for documentation and reporting.
Preferred Candidate:
2+ years of experience in Pharmaceutical Production/QC.
Basic knowledge of cGMP, GDP, SOPs, and validation activities.
Positive communication and documentation skills.
📌 Qc Laboratory Analyst Ahmedabad (India)
🏢 Ashkom
📍 India
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