Job description
About the role
Responsible for the process qualification, yield and manufacturing improvement.
What you’ll be doing
- Responsible to develop, configure, and optimize manufacturing processes.
- Responsible to develop best practices, routines, and innovative solutions to improve production rates and quality of output.
- Responsible to develop and maintain process documentation and operating instructions for the processes.
- Responsible for risk management evaluation e.g., FMEA
- Responsible for the qualifications for equipment and process (DQ/SAT/IQ/OQ/PQ).
- Ensure all the written procedures and working instructions for assembly and packaging are straightly observed, and all documents must be up to date.
- Ensure workplace are clean and safe to work all the time.
- Perform any other relevant responsibility that may be assigned occasionally as required by management or immediate superior.
What we’re looking for
Qualifications
- Degree in Science or Engineering, in any discipline.
Experience
- Minimum 2 – 5 years in process engineering, any medical manufacturing environment.
- Familiar with GMP and ISO 13485.