Perform regular internal quality audits to assess the compliance of manufacturing processes with established quality standards and requirement.
Generate or compile reports of audit findings, highlighting areas for improvement and follow up on corrective actions.
Perform process verification to ensure that manufacturing process are executed correctly and meet the defined standard and specification.
Support on the administration of calibration control of test and measurement equipment.
Support the regularly update and maintenance of documentation including ISO documents, Control Plan and Inspection Checklist and process verification records.
Perform data analysis and investigation based on customer feedback, identifying trends and areas for improvement.
Provide support and preparation for external audit such as customer audit, ISO audit, by ensuring relevant documentation, records are readily available and up to date.
Requirements:
Diploma in Engineering, Science, or relevant field.
Prior experience in a QA role, especially in supporting the Audit / Internal process improvement for manufacturing.
Familiarity with QA tools and methodology such as 8D (Eight Disciplines) Methodology, Mistake Proofing (POKA YOKE), Root Cause Analysis, and FMEA (Failure Mode and Effects Analysis).
Sound knowledge in statistical tools and software, such as Minitab, Tableau, or SPC.
Proficient in MS Office applications
Effective communication and interpersonal skills, with the ability to collaborate with cross-functional teams
Attention to detail and a commitment to maintaining high standards of quality.
Able to work in a cleanroom environment and open for 12-hours permanent day shift.
GMP Technologies (S) Pte Ltd | EA Licence 11C3793 | EA Personnel: Novita Widjaja | Registration No: R22105960
