THÔNG BÁO TUYỂN DỤNG – CÔNG TY DIVERSATEK

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RECRUITMENT

Introduction

Diversatek Vietnam is a member of the Diversatek Healthcare Group of medical technology companies. Diversatek opened its Vietnam manufacturing operation in Binh Duong, December 2010, representing a US high technology investment and continues to expand.

Recruitment

01 QUALITY SUPERVISOR

Requirement

  • University Degree in Engineering or equivalent experience
  • Have 2-3 years experience in quality and ISO system
  • Have experience in management
  • Proficient in English speaking and writing skill, Microsoft Office programs (Words, Excel) and CAD SOFTWARE (Autodesk Inventor, AutoCAD)
  • Well-organized, good people management skill and good problem-solving skill
  • Good communication skill
  • Self-starter/ Initiates personal tasks
  • Work 5.5 days/week and flexible time
  • Work at VSIP1, Thuan An City, Binh Duong Province

 

Job Description

  • Manages all inspection activities for Diversatek VN
  • Manages label printing systems.
  • Manages and executes Corrective Action & Preventive Action (CAPA) program.
  • Leads CAPA team and administers all CAPA investigations, activities, systems, and reports
  • Reviews and reports on effectiveness of all CAPA activities
  • Prepares Quality reports for Management Review meetings
  • Reviews and approves all Diversatek VN product, process and QMS changes (Engineering Change Orders – ECOs)
  • Manages and directs all Inspector activities and performs personnel reviews
  • Manages and directs all Quality activities and performs personnel reviews
  • Manages internal audit program of Diversatek VN quality system
  • Performs as part of company representative team for Food and Drug Administration (FDA), customer, or other regulatory agency audits
  • Directs supplier approval program. Reviews and approves new suppliers and assigns supplier level 4&5.
  • Manages controlled room monitoring and product bioburden monitoring.
  • Directs, monitor and execute training program.
  • Reviews all process and product validation protocols and reports.
  • Ensures Quality personnel follow all required ISO and FDA regulations as communicated through the Quality Management System.
  • Reviews and approves incoming receivers.
  • Performs training on all ECOs and all QMS changes.
  • Provides quality support for new projects including: sourcing materials and equipment, reviewing supplier qualifications against requirement, etc.,
  • Manages internal Non-Conformance Report (NCR) program
  • Reviews and approves all NCRs.
  • Manages and executes Complaint program.
  • Manages document control system including procedures, drawings, work instructions, part numbers assignments and labeling (physical and electronic).
  • Support purchasing in quality returns and corrective actions
  • Manages Approved Supplier List (ASL)
  • Manages and coordinates document control issues with external subcontractors
  • Manages calibration program.
  • Reviews and signs Certificates of Compliance (COC) for outgoing shipment as designated.
  • Direct, assign, instruct and check work of Quality Inspectors.

 

Salary & Policy

  • Competitive market salary
  • Professional and good working environment
  • Chance to develop career path

Please contact Ms. Nhan – Nhan.nguyen@diversatek.com/ngnhan2003@gmail.com