Pharma Production Technician – Cleanroom Packing & cGMP

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD.; Singapore; On-site; SGD 36,000 - 60,000; Full time

Job summary

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD. is seeking personnel for final packaging of tablets and capsules in a cleanroom environment in Tuas.

You will operate and maintain packing lines, ensure strict cGMP conformity, and document all batch processes. 2–5 years in pharmaceutical manufacturing is preferred, with strong teamwork and safety awareness. Responsibilities include in-process monitoring, qualification participation, and coordination with Engineering for line breakdowns, while

Qualifications

• Minimum GCE 'O' level or NITEC or Higher NITEC or Diploma in Biotechnology / Biomedical / Mechanical / Mechatronics Engineering or relevant disciplines.
• 2-5 years of manufacturing experience in Pharmaceutical or related industries.

Responsibilities

• Perform operations in tablet and capsule final packing equipment.
• Operate and clean packing equipment and maintain cleanliness of the equipment.
• Document operations in accordance with cGMP requirements.
• Follow SOPs and batch documents for equipment operation.
• Monitor in-process parameters and checks during batches.
• Complete records and documentation for packing and related equipment.
• Coordinate with Engineering for breakdown rectification of packing lines.
• Participate in equipment and process qualification.
• Investigate process deviations and compliance-related matters.
• Ensure compliance with GxP, safety and quality policies.

Education

GCE O' Level / NITEC / Higher NITEC / Diploma in Biotechnology / Biomedical / Mechanical / Mechatronics Engineering or relevant disciplines

Job description

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD. is seeking personnel for final packaging of tablets and capsules in a cleanroom environment in Tuas.

You will operate and maintain packing lines, ensure strict cGMP conformity, and document all batch processes. 2–5 years in pharmaceutical manufacturing is preferred, with strong teamwork and safety awareness. Responsibilities include in-process monitoring, qualification participation, and coordination with Engineering for line breakdowns, while