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KEY DUTIES AND RESPONSIBILITES:
.Perform various activities and tasks required in the tablet and capsule final packing equipment.
.Operate all relevant equipment, clean, assemble and maintain the cleanliness of the equipment.
.Perform and maintain the documentation of operations in accordance with cGMP requirement.
.Operate the equipment appropriately in accordance with Standard Operating Procedure / batch document.
.Perform online monitoring of in process parameters / checks throughout the batch.
.Complete all relevant records and other documentation required for packing and related equipment in the work area.
.Perform all activities in accordance with cGMP.
.Maintain the cleanliness of work area to ensure cGMP compliance.
.Perform all other relevant duties required to meet the schedule.
.Check relevant material and product details against batch document.
.Co-ordination with Engineering for break down rectification of both primary and secondary packing lines
.Involve in equipment / process qualification.
.Participate in investigation of process deviation, cGMP and all other compliance related matters, where applicable.
.Ensure compliance with GxP / Safety / Quality policies.
REQUIREMENT
.Good understanding of safe working practices and cGMP.
.Experience in bottle or blister oral solid dosage packing is preferred.
.A good team player with a positive learning attitude.
.Willing to work in Tuas area, in cleanroom environment with full gowning.
EDUCATION & EXPERIENCE
.Minimum GCE O level or NITEC or Higher NITEC or Diploma in Biotechnology / Biomedical / Mechanical / Mechatronics Engineering or relevant disciplines
.With 2-5 years of manufacturing experience in Pharmaceutical or related industries.
.Entry level NITEC / Higher NITEC / Diploma candidates are welcome to apply
Date Posted: 25/09/2025
Job ID: 127039191