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.
