Senior Engineer, Moulding

Medifox DAN GmbH; Singapore; On-site; SGD 110,000 - 170,000; Full time

Job summary

Medifox DAN GmbH seeks an experienced Mounding Engineer to drive advanced LSR moulding processes in a high-volume, medical-related manufacturing setting in Singapore. You will own process development, equipment validation, and cost- reduction initiatives while collaborating with production, quality and planning teams.

The role requires 5–10+ years in injection moulding, leadership capability, and strong analytical problem-solving skills to optimize OEE, scrap reduction and cycle times in a

Qualifications

• Bachelor's degree in Mechanical, Manufacturing, Polymer or Chemical Engineering.
• 5–10+ years of injection moulding experience.
• Strong hands-on experience in LSR moulding and multi-cavity mould processing.
• Experience in medical, automotive, or consumer product manufacturing.

Responsibilities

• Implement, maintain & improve LSR moulding processes, equipment, facilities and documentation.
• Lead and manage multiple projects; collaborate with cross-functional teams.
• Mentor or train junior engineers and technicians.
• Develop robust moulding processes and support trials/qualification.
• Reduce cycle time, scrap and manufacturing cost; improve OEE.

Skills

LSR moulding

Injection moulding

Process optimization

OEE improvement

Cross-functional collaboration

Education

Bachelor's Degree in Mechanical Engineering

Bachelor's Degree in Manufacturing Engineering

Bachelor's Degree in Polymer Engineering

Bachelor's Degree in Chemical Engineering

Tools

Mold Qualification

GD&T ASME Y14.5

Job description

The primary role of Mounding Engineering function is to apply advance skills and knowledge of mounding engineering in process, equipment, facilities and documents, in order to meet the current and future production volume, quality, OH&S and cost requirements. Key deliverables include conducting process validation, scrap reduction and cost saving initiatives.

Let’s talk about Responsibilities

• To implement, maintain & improve Liquid Silicone Rubber (LSR) Moulding Manufacturing processes, equipment, facilities and documentation to meet moulding production volumes and at all times follow OH&S guidelines.
• Possess Global mindset and ability to work with other geographical sites
• Lead & manage multiple Projects, Influence and Collaborate with other teams
• Lead, mentor or train junior engineers and technicians
• Develop robust moulding processes.
• Support mould trials and qualification.
• Reduce cycle time, Reduce Moulding Scrap and Manufacturing cost.
• Improve Overall Equipment Effectiveness (OEE).
• Investigate moulding defects and customer complaints.
• Work closely with Production, Planning, Quality, SQE, PD, PLE, GSA and Marketing teams
• Able to work independently without guidance in fast-paced and high-pressure environment
• Decision making based on data-driven and risk analysis
• Strong analytical and troubleshooting skills

• Leadership and mentoring capability
• Effective communication with cross-functional teams
• Continuous improvement mindset (Lean Manufacturing)

Let’s talk about Qualifications and Experience

Education:

• Bachelor's Degree in:
  • Mechanical Engineering
  • Manufacturing Engineering
  • Polymer Engineering
  • Chemical Engineering

Experience:

• 5 to 10+ years of injection moulding experience.
• Strong hands-on experience in:
  • LSR moulding
  • Multi-cavity mould processing
  • Medical, automotive, or consumer product manufacturing
  • High-volume automated manufacturing environments

Technical Skills:

• LSR material handling
• LSR moulding machine and dosing unit operation
• LSR Process optimization, Defects troubleshooting and Scrap reduction
• Mold Qualification and Accepance
• Tool Design Review
• Problem-Solving skills (such as DMAIC, Cause & Effect, 5 Whys)
• Automation and Robotic integration
• Able to read and interpret Mechanical Drawing
• Able to read and interpret GD&T ASME Y14.5-2018

Quality and Regulatory Knowledge:

• Statistical Process Control (Cpk, SPC)
• Hypothesis Test and Design of Experience
• PFMEA and Control Plans
• DQ/IQ/OQ/PQ process validation
• ISO 13485 (medical devices)
• Safety standards (ISO, OSHA)
• GMP requirements (for medical manufacturing)