Associate Production Engineer (Medical Robotics)

Uromedtech Pte Ltd

Queenstown

On-site

NZD 65,000 - 100,000

Full time

14 days+
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Job summary

Uromedtech Pte Ltd is seeking an Associate Production Engineer to serve as the technical lead for assembling and delivering precision robotic prostate biopsy systems. You will bridge R&D, manufacturing, and clinical teams to ensure every unit matches exact specifications.

You will manage production workflow, troubleshoot electromechanical issues, and drive DFM initiatives to prepare the platform for future ablation therapy, with seniority determined by MedTech experience and leadership potential.

Qualifications

  • Education: Diploma and above in Mechanical, Mechatronics, or Biomedical Engineering.
  • Experience: 1–3 years in medical device manufacturing or high-precision robotics.
  • Technical Skills: Read drawings and schematics; assemble machinery/robotic sub-assemblies; ERP and CAD inputs (SolidWorks) are a plus.
  • Mindset: Quality-First attitude in a fast-paced startup environment.

Responsibilities

  • Lead Assembly: hands-on assembly of robotic positioning systems and associated hardware.
  • Create and refine Work Instructions (WI) and SOPs for consistent builds.
  • Troubleshoot hardware/software issues during builds with R&D support.
  • DFM/DFS: translate assembly challenges into ECRs to improve manufacturability and serviceability.
  • Tooling and jigs: provide inputs for calibration tools to improve efficiency and accuracy.
  • V&V Support: assist with verification and validation activities for hardware upgrades.
  • Production Planning and BOM: liaise with vendors and coordinate schedules for timely delivery to clinical sites.
  • Manage ERP records and ERP integration with BOM and inbound/outbound inventory.
  • Oversee packaging and logistics for compliant medical device shipment.
  • DHR/NCR: own Device History Record completion; investigate NCRs and drive corrective actions.
  • Maintain ISO 13485/FDA QSR-compliant, 5S production environment.

Skills

Reading drawings
Schematic understanding
Quality mindset

Education

Diploma or higher in Mechanical Engineering
Diploma or higher in Mechatronics Engineering
Diploma or higher in Biomedical Engineering

Tools

ERP software
CAD SolidWorks

Job description

As the Associate 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, and the clinic, 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. Candidate seniority (Associate vs. Full) will be determined by the depth of prior MedTech experience and leadership potential.

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.
  • Shipping & Logistics: Oversee the secure packaging and preparation of medical devices for shipment, ensuring all logistical compliance is met.
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
Education:

Diploma and above in Mechanical, Mechatronics, or Biomedical Engineering.

Experience:

1–3 years in medical device manufacturing or high-precision robotics.

Technical Skills:
  • 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.
Mindset:

A "Quality-First" attitude with the agility to work in a fast-paced startup environment.

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