QFS Supervisor _ Cashew Bien Hoa II

Mô tả Công việc
1. QMS: follow guideline of QFS manager to prepare SOP, collaboration with sites to develop, implement and maintain QMS system follow global STD, GFSI standard, customer expectation to all sites and following up on executions.
2. Collect data from the sites, (e.g. KPI tracking report, customer complaint, CAPA, testing, cost, Certification status report, FSVP status report, FDA registration status report, ...) do analysis, reporting monthly, quarterly, yearly or depend on top management request.
3. FDA Alert monthly report /RASFF monthly report
4. Regulatory update including export market and local regulation monthly update, other reports once required (global FSQ reports, MOR report...)
5. Set up FSQ meeting with all sites in Regional; Critical complaint meetings with site management team to solve the issue (escalated cases); Cascading meetings with all sites to deploy FSQ plans; Other meetings as needed (sharing & learning calls, training sessions, ...) recording MoM, following up on aligned action plan.
6. Supporting audits (certification audits, customer audits) when required providing required documents to support the audit, participating audits to help team answering tough questions from auditors, joining closing meeting to influence the auditor decisions.
7. Standardization/ Optimization: new SOPs, Testing methods, frequency, work with service to help sites can find to solution for improve.
8. Regulatory review in conjunction with NPD team in new product projects
Surveys (FSQ culture, polls, other projects...).