06 Aug
|
Ashkom
|
Ahmedabad
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.
- Valuable communication and documentation skills.
📌 QC Laboratory Analyst (Ahmedabad)
🏢 Ashkom
📍 Ahmedabad