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.

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.