Assists In-process Quality Engineer to monitor the compliance and effectiveness of the established system and request corrective action for detected infraction.
Monitor that the equipment, tooling, process, operator is qualified and fit to use in the line.
Assists Engineer in ensuring CA/PA implementation and validate the effectiveness.
Monitor and ensure the implementation of the established system and assess the effective。
Implementation of SPC and other quality tools as necessary.
To perform and lead IPQA to do regular process/standard operation audit and take improvement with the team.
To update and perfect IPQA audit checklist based on the requirement.
To do internal audit and assist Engineer to do customer audit. Perform medical equipment assembly’s process buy-off, escalate to Engineer when abnormality detected.
Job Requirement:
Candidate must possess at least diploma or above in electronics / mechanical / manufacturing engineering or equivalent.
At least 1 years working experience in the manufacturing field
Knowledge in ISO 9001 and 13485 will be add advantage.