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Manufacturing Operations
180003KD Requisition #

Main Purpose:


  • Ensure manufacturing operations, under the supervision of team leader/ manufacturing supervisor in order to assemble medical devices according to good manufacturing practice, manufacturing flow, standard operating procedures and safety procedures.


Key Accountabilities: 


·        Produces medical devices according to the validated procedure.

·        Demonstrates the understanding and significance of line clearance, work station preparation and other Good Manufacturing Practices (GMP) procedures/ and Quality System Requirements.

·        Maintains a thorough understanding of the acceptance criteria for the specific operation(s) being performed.

·        Accurately documents information on history records, inspection data sheets, scrap reports, and other documentation related to specific processes being performed.

·        Supports and provides manufacturing training to new assembler.

·        Complies with all Controlled Environment Area (CEA) protocol, including personal hygiene, gowning procedures, and safety procedures.

·        Demonstrates the ability to work as a team member in a manner that is conducive to a positive work environment.

·        Actively participates in daily tier 1 meeting, giving feedback and contribute continuous improvement ideas.

·        Follow team leader’s/ manufacturing supervisor’s instructions and highlight for any abnormality.

Experience and Knowledge:


·        Able to read and write English

·        Proficient in using computer

·        Sensitive to quality and applicable procedures respect

·        Being able to work with a microscope

·        Being able to explain clearly and accurately manufacturing issue

·        Used to work in technical environment with manufacturing equipment is a plus

·        Used to work in a cleanroom environment is a plus




·        Secondary education and/or manufacturing experience

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