Cleanroom Operator

The Cleanroom Operator is responsible for performing valve assembly and related manufacturing activities in a controlled cleanroom environment. The role ensures products are assembled according to work instructions, engineering specifications, quality requirements, and cleanroom protocols while meeting production targets and maintaining a high standard of cleanliness and product integrity.

Key Responsibilities

• Perform valve assembly operations according to approved Work Instructions, drawings, specifications, and production requirements.
• Assemble, inspect, clean, and handle valve components using approved tools, equipment, and processes.
• Follow established cleanroom procedures, gowning requirements, contamination-control practices, and environmental requirements.
• Perform pre-assembly preparation, component verification, cleaning, assembly, and post-assembly activities as assigned.
• Verify part numbers, quantities, specifications, and material identification before starting assembly.
• Use hand tools, torque tools, fixtures, gauges, and other approved equipment correctly and safely.
• Perform in-process inspections and basic measurements to ensure components and assemblies meet quality requirements.
• Identify and report defects, abnormal conditions, damaged components, or process deviations to the Supervisor or Quality team.
• Complete production records, inspection records, checklists, and other required documentation accurately and in a timely manner.
• Maintain product traceability throughout the assembly process.
• Achieve assigned daily production targets while maintaining required quality standards.
• Follow ESD, FOD, contamination-control, and other applicable cleanroom requirements.
• Maintain cleanliness and organization of the workstation in accordance with 5S and cleanroom standards.
• Handle components and finished assemblies carefully to prevent contamination, damage, or product mix-up.
• Perform routine checks of tools, fixtures, and equipment and report any abnormalities or malfunctions.
• Support continuous improvement activities to improve safety, quality, productivity, and process efficiency.
• Comply with all company policies, safety procedures, PPE requirements, and cleanroom regulations.
• Perform other duties as assigned by the Supervisor or Management.

Job Requirements

• Minimum SPM / equivalent qualification.
• Previous experience in cleanroom manufacturing, precision assembly, semiconductor, medical device, valve assembly, or similar manufacturing environment is an advantage.
• Experience in mechanical assembly or using hand tools is an advantage.
• Able to read and follow Work Instructions, visual aids, and basic technical documentation.
• Able to perform repetitive assembly work with a high level of accuracy and attention to detail.
• Able to work in a controlled cleanroom environment and comply with gowning and contamination-control requirements.
• Able to work shifts, overtime, weekends, or public holidays when required by business needs.
• Good hand-eye coordination and manual dexterity.
• Good attendance, discipline, teamwork, and willingness to learn.
• Safety-conscious and committed to maintaining product quality.