Production Engineer (Medical Robotics)

UROMEDTECH PTE. LTD.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

UROMEDTECH PTE. LTD.

in Singapore seeks a Production Engineer to lead the assembly and delivery of our precision robotic prostate biopsy systems, bridging R&D and manufacturing to ensure every unit meets exact specifications. You will manage the production workflow, troubleshoot electromechanical issues, drive DFM initiatives, and contribute toward a path to Production Manager in a fast paced startup environment.

Qualifications

• Diploma or higher in Mechanical or Mechatronics Engineering.
• 1–3 years in medical device manufacturing or high‑precision robotics.
• Ability to read drawings, circuit diagrams, and technical specifications.
• Proven ability to assemble machinery/robotic sub‑assemblies with high repeatability.
• Proficiency with ERP software and CAD (SolidWorks) for DFM inputs is an advantage.
• Basic understanding of medical device deployment and robotic calibration.
• Quality‑First attitude and ability to work in a fast‑paced startup environment.

Responsibilities

• Lead Assembly: Hands‑on assembly of robotic positioning systems, integrated ultrasound hardware, and MRI‑fusion workstations.
• Work Instructions: Execute and refine WI and SOPs to ensure consistent builds.
• Troubleshooting: Resolve hardware/software issues during the build phase in collaboration with R&D.
• Manufacturing Feedback Loop: Translate assembly challenges into Engineering Change Requests (ECR) to improve manufacturability and serviceability.
• Tooling & Jigs: Provide inputs for jigs or calibration tools to improve efficiency and accuracy.
• V&V Support: Assist R&D in Verification and Validation activities for hardware upgrades.
• Production Planning: Liaise with vendors and suppliers, coordinate production schedules to meet forecasts.
• BOM & ERP Management: Maintain BOM and manage inventory records using the ERP system.
• Site Management: Maintain a 5S‑compliant, audit‑ready production environment (ISO 13485/FDA QSR).

Skills

Read drawings

Circuit diagrams

Technical specs

Robot assemblies

DFM mindset

Education

Diploma in Mechanical or Mechatronics Engineering

Tools

SolidWorks

ERP software

Job description

As the Production Engineer, you will be the technical lead for the assembly and delivery of our precision robotic prostate biopsy systems. As part of the link between R&D, the manufacturing line, you will play a pivotal role in ensuring that every unit is built to exact specifications.

You will also be expected to manage the production workflow, help troubleshoot electromechanical issues, and drive \"Design for Manufacturing\" (DFM) initiatives to prepare our platform for the next horizon of ablation therapy.

We are looking for a high-potential engineer with a trajectory toward Production Manager.

Key Responsibilities

Technical Manufacturing & Assembly

• Lead Assembly: Hands‑on assembly of robotic positioning systems, integrated ultrasound hardware, and MRI‑fusion workstations.
• Work Instructions: Execute and refine Work Instructions (WI) and Standard Operating Procedures (SOPs) to ensure consistent builds.
• Troubleshooting: Act as the first line of defense, and in collaboration with R&D, to resolve hardware/software issues during the build phase.

Design Transfer & Continuous Improvement (DFM/DFS)

• Manufacturing Feedback Loop: Translate assembly challenges into Engineering Change Requests (ECR) to improve manufacturability and serviceability.
• Tooling & Jigs: Utilize and provide inputs/feedback for jigs or calibration tools to improve efficiency, increase accuracy, and reduce \"Procedure Time\" variability.
• V&V Support: Assist R&D in Verification and Validation (V&V) activities for hardware upgrades and new robotic features.

Operations & Supply Chain Management

• Production Planning: Liaise with vendors and suppliers, and coordinate production schedules based on the commercial forecast to ensure timely delivery to clinical sites.
• BOM & ERP Management: Maintain the Bill of Materials (BOM) and manage inbound/outbound inventory records using the ERP system.

Quality & Regulatory Compliance (Liaison with QC)

• DHR Ownership: Responsible for the accurate completion of the Device History Record (DHR) for each unit produced.
• NCR Participation: Identify and document Non‑Conformances (NCR). Work closely with the QC Engineer to investigate root causes and implement corrective actions.
• Site Management: Maintain a 5S‑compliant, organized, and audit‑ready production environment (ISO 13485/FDA QSR).

Requirements & Qualifications

• Diploma and above in Mechanical, Mechatronics Engineering.
• 1-3 years in medical device manufacturing or high‑precision robotics.
• Ability to read drawings, circuit diagrams, and technical specifications.
• Proven ability to assemble machinery/robotic sub‑assemblies, including gearboxes, actuators, and sensor arrays, with high repeatability.
• Proficiency with ERP software and CAD (SolidWorks) for DFM inputs is an advantage.
• Basic understanding of medical device deployment and robotic calibration.
• A \"Quality-First\" attitude with the agility to work in a fast‑paced startup environment.