KEY DUTIES AND RESPONSIBILITES:
- Perform various activities and tasks required in 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 of granulation/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.
REQUIREMENTS:
- 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 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.
