Manufacturing Operator I

Job Description 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 Requirements 02 years in pharma/biotech/manufacturing (freshers with relevant exposure can apply). Bachelor's in Life Sciences / Biotechnology / related field. Mandatory Requirements Basic cGMP knowledge. Aseptic technique awareness. SOP & documentation (GDP) understanding. Attention to detail and teamwork.