What are the responsibilities and job description for the Manufacturing Operator I position at Katalyst CRO?
Job Description
Supports cGMP manufacturing suites by ensuring proper stocking, cleaning, material preparation, and equipment maintenance while following GMP and aseptic practices.
Responsibilities
Supports cGMP manufacturing suites by ensuring proper stocking, cleaning, material preparation, and equipment maintenance while following GMP and aseptic practices.
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.
- 02 years in pharma/biotech/manufacturing (freshers with relevant exposure can apply).
- Bachelors in Life Sciences / Biotechnology / related field.
- Basic cGMP knowledge.
- Aseptic technique awareness.
- SOP & documentation (GDP) understanding.
- Attention to detail and teamwork.