KEY DUTIES AND RESPONSIBILITES:
· Perform various activities and tasks requiredin the granulation and blending production areas.
· 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 granulation/blending, maintenance and cleaning of 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 ofgranulation/blending equipment.
· Involve in equipment / process qualification.
· Participate in investigation of process deviation, cGMP and all other compliance related matters, where applicable.
· Ensure compliance to GxP / Safety / Quality policies.
REQUIREMENT
· Good understanding of safe working practices and cGMP.
· Experience in granulation and blending process of oral solid dosage manufacturing is preferred.
· A good team player with positive learning attitude.
· Willing to work 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.
