Production Technical Operator II GMP Cleanroom

Alcon

Singapore

On-site

SGD 36,000 - 54,000

Full time

3 days ago
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Job summary

Alcon is seeking a Technician II, Production Technical Operations in Singapore to operate automated manufacturing and packaging equipment in a cleanroom environment. You will ensure contact lenses are produced to the highest quality standards, complying with cGMP, GDP, and regulatory requirements, while supporting continuous improvement initiatives.

The role requires a NITEC in engineering disciplines and at least 2 years of manufacturing experience, preferably in GMP-regulated settings.

Qualifications

  • Strong teamwork and communication skills.
  • Willingness to work on rotating shifts, weekends and public holidays.
  • Familiarity with GMP/GDP practices and cleanroom environments.

Responsibilities

  • Operate automated manufacturing and packaging equipment in a controlled cleanroom.
  • Ensure products meet quality standards and regulatory requirements (GMP, HSE, Data Integrity).
  • Collaborate with cross-functional teams to meet production targets and uptime goals.
  • Conduct In-Process Checks and visual inspections to ensure product quality.
  • Coordinate sterilization scheduling to maintain product integrity.
  • Perform simple machine setups and equipment maintenance as needed.
  • Uphold 5S housekeeping and participate in Kaizen/continuous improvement initiatives.

Skills

Teamwork
Communication
Problem-solving
Willingness to rotate shifts

Education

NITEC in Mechanical Engineering/Mechatronics/Electrical/Automation

Job description

Alcon is seeking a Technician II, Production Technical Operations in Singapore to operate automated manufacturing and packaging equipment in a cleanroom environment. You will ensure contact lenses are produced to the highest quality standards, complying with cGMP, GDP, and regulatory requirements, while supporting continuous improvement initiatives.

The role requires a NITEC in engineering disciplines and at least 2 years of manufacturing experience, preferably in GMP-regulated settings.

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