Incoming Quality Inspector II - Clean Room QC

BIOTRONIK

Singapore

On-site

SGD 36,000 - 58,000

Full time

14 days+
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Benefits offered by this job

Being entrepreneurial in spirit
Global teams and projects
Professional development

Job summary

BIOTRONIK is a leading medical devices company in cardiology, with operations in Singapore. The Quality Control Inspector II, Incoming Quality will oversee and perform incoming quality inspections in a clean room environment, aligned to BIOTRONIK specifications under cGMP and the Quality System.

You will analyze data, generate records, and support approvals and training as required. Role requires 2 years in a regulated manufacturing quality tech, familiarity with CMM/vision systems, and SAP/MES

Qualifications

  • Quality inspections techniques and experience with measuring instruments.
  • Familiarity with inspection tools like CMM, smart scope or vision systems preferred.
  • Understanding of technical drawings and GD&T fundamentals.

Responsibilities

  • Oversee incoming inspection operations in line with cGMP and QM requirements.
  • Perform mechanical/visual/functional inspections per procedures and specs.
  • Dispost non-conformities timely and block products for investigation.
  • Generate inspection records for materials lots and NCRs as needed.
  • Support First article/First Piece approvals and plan daily inspections.
  • Maintain inspection records and archive documents as required.
  • Assist in training and certification of inspection specs.

Skills

Quality inspections
Measuring instruments
Technical drawings
SAP experience
MES experience
Communication

Education

GCE O Level / ITE / NITEC

Tools

SAP
MES

Job description

BIOTRONIK is a leading medical devices company in cardiology, with operations in Singapore. The Quality Control Inspector II, Incoming Quality will oversee and perform incoming quality inspections in a clean room environment, aligned to BIOTRONIK specifications under cGMP and the Quality System.

You will analyze data, generate records, and support approvals and training as required. Role requires 2 years in a regulated manufacturing quality tech, familiarity with CMM/vision systems, and SAP/MES

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