Job Description
Summary:
Key Responsibilities:
Experience:
- Supports cGMP manufacturing suites by ensuring proper stocking, cleaning, material preparation, and equipment maintenance while following GMP and aseptic practices.
Key Responsibilities:
- Perform daily 6S, stocking, and cleaning of suites and parts
- Prepare, assemble, and autoclave materials for production
- Handle material movement across production areas
- Perform routine equipment maintenance and cleaning
- Complete weekly/monthly cleaning (e.g., inoculum rooms)
- Maintain GMP/GDP-compliant documentation
- Follow aseptic techniques and contamination control practices
- Support training, meetings, and assigned tasks
Experience:
- 0–2 years in pharma/biotech/manufacturing (freshers with relevant exposure can apply)