Assembler I
- 📅
- 180003KD Numéro de demande de personnel
- 📅
- Mar 01, 2018 Date de publication
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
Qualifications:
·
Secondary education and/or manufacturing
experience
