Senior Mfg Engineer: Injection Molding & Medical Devices

TALENTVUE PTE. LTD.

Singapore

On-site

SGD 80,000 - 120,000

Full time

7 days ago
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Job summary

TALENTVUE PTE. LTD. in Singapore seeks a Manufacturing Engineer to optimize high‑volume biomedical device manufacturing processes. You will develop tooling, support NPI, and drive process validations to ensure quality and efficiency.

Applicants should have a Bachelor’s degree in engineering and 5–8 years of manufacturing engineering experience, ideally in medical devices such as catheters, with strong knowledge of DOE, FMEA, IQ/OQ/PQ, and GMP/ISO 13485 requirements.

Qualifications

  • Bachelor's degree in engineering or related technical field.
  • 5–8 years of manufacturing engineering experience in a high-volume production environment.
  • Medical device manufacturing experience, preferably catheter production, is an advantage.
  • Strong knowledge of process validation, DOE, statistical analysis, FMEA, IQ/OQ/PQ, and GMP/ISO 13485 requirements.

Responsibilities

  • Develop, optimize, and troubleshoot manufacturing processes, tooling, and fixtures.
  • Support new product introduction (NPI), process transfers, and process validations (IQ/OQ/PQ).
  • Drive continuous improvement initiatives to improve yield, throughput, and operational efficiency.
  • Conduct root cause analysis and implement corrective actions for manufacturing issues.
  • Support equipment qualification, maintenance coordination, and process capability studies.
  • Ensure compliance with GMP, ISO 13485, FDA regulations, and quality system requirements.
  • Prepare and maintain manufacturing documentation, validation protocols, and technical reports.

Skills

Manufacturing engineering
DOE
Statistical analysis
FMEA
IQ/OQ/PQ
GMP/ISO 13485
Process validation

Education

Bachelor's Degree in Engineering

Job description

TALENTVUE PTE. LTD. in Singapore seeks a Manufacturing Engineer to optimize high‑volume biomedical device manufacturing processes. You will develop tooling, support NPI, and drive process validations to ensure quality and efficiency.

Applicants should have a Bachelor’s degree in engineering and 5–8 years of manufacturing engineering experience, ideally in medical devices such as catheters, with strong knowledge of DOE, FMEA, IQ/OQ/PQ, and GMP/ISO 13485 requirements.

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