Process/R&D Engineer with 5 years of experience in medical device and semiconductor manufacturing, specialising in process development, equipment engineering, NPI, validation, and quality improvement. Experienced in IQ/OQ/PQ, process optimisation, DOE, RCA, CAPA, FMEA, SPC, technical documentation, and regulated manufacturing environments including ISO 13485. Skilled in supporting manufacturing teams with practical engineering solutions that improve yield, compliance, quality, and operational efficiency.
We will review the reports from both freelancer and employer to give the best decision. It will take 3-5 business days for reviewing after receiving two reports.