The Trial Master File (TMF) Study Owner (SO) Lead provides managerial oversight of document management deliverables of assigned TMF Study Owners (SOs) and/or document processing staff (e.g., TMF Study Owner Associates, TMF Document Specialists). The TMF SO Lead: Is
The Project Manager will be mainly responsible to drive all the program launches on time and budget, ensure to achieve all customer and company requirements for (new or changed products) programs including quality, cost, delivery, product performance
General Description The Supplier Development Engineer will lead and implement quality initiatives. Manage and document the activities between company and suppliers on all product quality issues. This position is a key partner to ensure accountability and quality
Job Summary Job Description JOB RESPONSIBILITIES (1) Collect and review Device Master Record (DMR) documents for Medline products subject to the regulatory requirements and project development plan; (2) Establish inspection criteria of new finished products, update and
System Development Lead acts as the overall technical owner for product systems, accountable for consistency and technical route selection; oversees cross-disciplinary design and integrates departmental solutions into actionable deliverables to meet product goals for performance, cost,
Job SummaryQA Specialist is responsible for quality assurance on the procedures of DMR and inspection criteria development and maintenance. Work closely with divisional QA and Asia stakeholders to ensure requirements are met under ISO13458 and CFR820.
Location(s) Wuhan, Hubei Company Molex Career Field Administrative Support Job Number 190719 What You Will Do 1. Responsible for collect and offer I/E documents to customs as request. 负责收集进出口文件，并按照要求提供给海关。 2. Responsible for daily team work and communication