Technician - Production (Compression) at PHARMAGEND GLOBAL MEDICAL SERVICES PTE LTD
Singapore, , Singapore -
Full Time


Start Date

Immediate

Expiry Date

31 Oct, 25

Salary

4000.0

Posted On

03 Aug, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Mechanical or Industrial Engineering

Description

REQUIREMENT

  • Good understanding of safe working practices and cGMP.
  • Experience in tablet compression machine or related tableting press.
  • 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.
Responsibilities
  • Perform various activities and tasks required in the Compression machines.
  • 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, 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 Compression 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.
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