Manufacturing Operator

Summary

• 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)

Education

• 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