Director, Industrial Engineering

Sonova Singapore Private Limited; Singapore; Hybrid; SGD 180,000 - 320,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Sonova Singapore Private Limited is seeking an Industrial Engineering Director to lead manufacturing process design, ERP data integrity, and continuous improvement for precision medical device production. This role interfaces with engineering, quality, operations and regulatory functions to drive compliant, scalable manufacturing.

You will own ERP BOMs and routings, drive cycle time reductions, lead ECM/ECO processes, and advance Lean Six Sigma initiatives across high-mix, low-volume assembly.

Qualifications

• Bachelor's or Master's degree in Industrial, Mechanical, or Manufacturing Engineering (or related)
• Hands-on ERP experience (BOM structuring, routing setup, cycle time data management)
• Experience with ISO 13485 and design controls under 21 CFR 820.30 / EU MDR

Responsibilities

• Own BOM maintenance in ERP and manage version control across active products
• Set up and maintain Manufacturing Process routings and cycle times in ERP
• Lead cycle time studies, line balancing, and productivity initiatives across assembly and sub-assembly operations
• Guide Engineering Change Management (ECM/ECO) processes with cross-functional review and documentation
• Ensure compliance with ISO 13485 and regulatory requirements (FDA 21 CFR 820, EU MDR)
• Lead or support Process FMEA, Process Validation, and product investigations tied to manufacturing processes

Skills

ERP data ownership

BOM maintenance

Routing setup

Cycle time data management

Lean Six Sigma

Cross-functional collaboration

Regulatory awareness

Education

Bachelor's or Master's in Industrial/Manufacturing Engineering

Tools

SAP

Oracle ERP

Job description

As the Industrial Engineering Director, you will lead manufacturing process design, ERP data integrity, and continuous improvement for hearing aid (or related medical device) manufacturing operations. This role bridges engineering, quality, operations, and regulatory functions to ensure efficient, compliant, and scalable manufacturing of miniaturized precision medical devices.

In this role, you will be in charge of:

• ERP & Manufacturing Data Ownership

  • Own Bill of Material (BOM) maintenance in ERP, ensuring accuracy and version control across all active products
  • Set up and maintain Manufacturing Process routings and corresponding cycle times in ERP
  • Ensure ERP data integrity supports accurate costing, capacity planning, and production scheduling

• Process Optimization & Productivity

  • Own cycle time studies, line balancing, and cycle time reduction activities across assembly and sub-assembly operations
  • Lead productivity, yield improvement, and scrap reduction initiatives across manufacturing lines
  • Drive continuous improvement using Lean/Six Sigma methodologies for high-mix, low-volume precision assembly

• Engineering Change & Qualification Management

  • Lead the Engineering Change Management (ECM/ECO) process, ensuring cross-functional review, impact assessment, and proper documentation
  • Execute engineering qualification of alternate source components and manufacturing processes, ensuring form, fit, and function equivalence
  • Partner with R&D and Value Engineering (VE) teams on design-for-manufacturability/assembly (DFM/A) reviews

• Quality & Regulatory Compliance

  • Ensure manufacturing processes comply with ISO 13485 (QMS) and applicable regional medical device regulations (FDA 21 CFR 820, EU MDR)
  • Lead or support Process FMEA, Process Validation (IQ/OQ/PQ), and Product Quality Investigations tied to manufacturing processes
  • Maintain documentation and traceability to support audits and regulatory inspections

• Leadership & Cross-Functional Collaboration

  • Manage a team of industrial/process/manufacturing engineers
  • Partner with Operations, Supply Chain, R&D, and Quality on manufacturing roadmaps and NPI readiness

Your background:

• Bachelor's or Master's degree in Industrial, Mechanical, or Manufacturing Engineering (or related)
• 8–10+ years in manufacturing/industrial engineering. Experience in medical device or precision electronics manufacturing will be an advantage
• Hands-on ERP experience (BOM structuring, routing setup, cycle time data management) — SAP, Oracle, or similar
• Deep knowledge of ISO 13485 and design controls under 21 CFR 820.30 / EU MDR
• Experience leading Engineering Change Management processes in a regulated environment
• Proven track record in cycle time reduction, line balancing, and yield/scrap improvement
• Experience with component/process qualification (alternate sourcing, second-source validation)
• Six Sigma or equivalent Lean certification will be preferred

How we work:

At Sonova, we prioritize the well‑being of our employees and foster an inclusive environment that promotes engagement and collaboration. Our team‑customized hybrid work model empowers teams to balance individual needs with business goals, offering flexibility and individualized time management. We recognize the importance of life outside of work and strive to create a supportive and motivating workplace where innovation thrives.