Ivana Stankovská

• Global PCBA & EMS Management: Oversee quality performance, continuous improvement, and escalations for international Tier-1 and Tier-2 suppliers of PCBA and electronic modules.
• VDA 6.3 Process Audits: Lead and execute on-site VDA 6.3 process audits focusing on modules P5, P6, and P7 as Lead Auditor, verifying supplier manufacturing capabilities, SMT lines, and corrective action closure.
• Electronics & IPC Standards: Enforce strict compliance with IPC-A-610 standards, reflow profiling, selective soldering, SPI/AOI/AXI inspection controls, and ESD protection (IEC 61340-5-1).
• APQP & PPAP Execution: Lead PPAP documentation reviews and approvals (PSW, Control Plans, PFMEA, Run@Rate, MSA, Cp/Cpk validation) for new product introductions and engineering change orders.
• Problem Solving & Escalations: Drive supplier root-cause investigations using 8D methodology, 5-Why, and Ishikawa diagrams to eliminate recurring line issues and manage containment actions.
• Supplier Development & Commercials: Manage Top Worst Supplier recovery programs, monitor supplier KPIs (PPM, on-time closure of 8Ds), and handle supplier chargebacks for non-conforming costs.

Served as the primary plant escalation interface for incoming component non-conformities and line stops.

Monitored plant supplier PPM, reviewed incoming 8D reports, and managed MRB/scrap disposition

Conducted supplier chargebacks for costs associated with non-conforming material.

Conducted incoming, in-process, and final quality inspections on production lines, ensuring compliance with control plans and technical drawings to maintain product standards.

Prepared daily quality reports, monitored scrap rates, and maintained Pareto defect tracking charts.

Conducted planned measurements and testing using laboratory equipment to verify product compliance.

Coordinated inspections and physical testing of incoming materials per approved sampling plans (AQL) to ensure compliance in regulated medical manufacturing.

Handled raw material and supplier non-conformities, recorded deviations in the TrackWise system, and initiated supplier claims.

Supported supplier 8D root-cause investigations and tracked corrective action status.

Communicated non-conformities directly with international raw material suppliers and internal production teams.