QA Engineer II: Incoming Quality & QMS Lead

Sanmina Corporation

Singapore

On-site

SGD 90,000 - 130,000

Full time

12 hours ago
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Job summary

Sanmina Corporation in Singapore seeks an Engineer II (QA) to lead incoming quality control initiatives, manage inspection plans and FAI documentation, and uphold stringent QMS and regulatory compliance. You will guide IQE/IQA teams, coordinate audits, and drive continuous improvement in product quality and process efficiency.

The role requires a degree or diploma in electronics/mechanical/manufacturing engineering, experience in electronics manufacturing, and familiarity with ISO and FDA/PMDA

Qualifications

  • Minimum Degree or Diploma in Electronics / Mechanical / Manufacturing Engineering or equivalent.
  • Experience in the electronics manufacturing environment as QA Engineer or related fields.
  • Knowledge of ISO 9001, ISO 14001, ISO 13485 and FDA/PMDA requirements preferred.

Responsibilities

  • Lead and maintain plant procedures for Incoming Quality and related forms and ensure QMS compliance.
  • Oversee creation and management of incoming parts inspection plans per customer specs and NPI.
  • Oversee FAI requirements and documentation for new/revised parts; ensure timely qualifications and records.

Skills

Quality Assurance
QA Engineer
Project Management
Lean Six Sigma
Audit / Compliance
Analytical Thinking

Education

Bachelor's or Diploma in Electronics / Mechanical / Manufacturing Engineering

Tools

Agile PQM
Agile PLM
Receiving Maestro
Inspection Maestro
MRB
Oracle
Looker Studio

Job description

Sanmina Corporation in Singapore seeks an Engineer II (QA) to lead incoming quality control initiatives, manage inspection plans and FAI documentation, and uphold stringent QMS and regulatory compliance. You will guide IQE/IQA teams, coordinate audits, and drive continuous improvement in product quality and process efficiency.

The role requires a degree or diploma in electronics/mechanical/manufacturing engineering, experience in electronics manufacturing, and familiarity with ISO and FDA/PMDA

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