QC Inspector cum Equipment Technician

Merlin MD Pte Ltd

Singapore

On-site

SGD 30,000 - 52,000

Full time

14 days+

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Job summary

Merlin MD Pte Ltd in Singapore is seeking a Quality Control Inspector to perform inspections on incoming, in-process, and finished products. The role emphasizes strict adherence to SOPs, cleanroom protocols, and accurate documentation to ensure traceability across the manufacturing process.

The candidate should have 1+ year of QC experience in medical devices or life sciences, strong attention to detail, and the ability to work independently with minimal supervision.

Qualifications

  • GCE 'N' Level or SPM or higher is required.
  • 1+ year experience in QC inspection in medical devices, pharma, or life sciences.
  • Able to read and follow SOPs and inspection documents.

Responsibilities

  • Perform QC inspections of incoming, in-process, and finished products per procedures.
  • Verify packaging and labeling meet specifications.
  • Prepare inspection records that are accurate and traceable.

Skills

SOP knowledge
Cleanroom procedures
Documentation
Verbal & written communication
Independent work
Basic computer skills
Inspection techniques

Education

GCE 'N' Level / SPM or higher
Diploma preferred

Tools

Measuring instruments
Quality test equipment
Sampling techniques/plans

Job description

Primary Job Responsibilities:
  • Perform quality inspections of incoming, in-process, and finished products according to quality procedures and instructions.
  • Verify that the inspected parts/materials, including packaging and labelling, meet specifications.
  • Prepare quality records after inspection completion. Ensure that the records are accurate and traceable.
  • Perform a variety of inspection methods and techniques such as visual inspection, dimensional measurements, and functional testing to determine the quality of products and component parts.
  • Able to identify recurring quality issues and support the implementation of improvement measures.
  • Maintain and clean QC equipment and instruments (i.e., microscope, gauges).
  • Complies with all Controlled Environment Room (CER) protocol, including personal hygiene, gowning, and safety procedures.
  • Participate in non-conformance materials and MRB activities related to QC inspection aspects.
Secondary Job Responsibilities:
  • Assist QC Executive on maintaining documentation.
  • Completes preventive maintenance requirements.
  • Observes equipment in operation to troubleshoot problems and ensure the proper functioning of the machines.
  • Removes defective components and replaces them with new ones.
  • Maintains inventory of spare parts for equipment.
  • Ensures all mechanical/electrical equipment supporting the facility is maintained and functioning properly.
  • Schedules any servicing that is required by 3rdparty to maintain facility requirements.
  • Ensures all documentation and service reports are completed and given to document control.
  • Any other tasks or projects that are being assigned by the immediate supervisor, as and when required.
Minimum Education Required:
  • GCE "N" level or Higher
  • SPM Level or Higher
  • Diploma Preferred
Additional Skills Required:
  • Working knowledge of current industry practices, SOP and cleanroom procedures.
  • Basic Computer Skills.
  • Able to communicate, both verbal and written, effectively and clearly.
  • Able to read and follow SOP or any required documents needed to carry out inspection.
  • Able to work independently with minimal supervision.
  • Able to work with assigned equipment and to describe mechanical problems as they arise.
Minimum Experience:
  • A minimum of one year's experience as a quality control inspector or equivalent in the medical device, pharmaceutical, or life sciences industries.
  • Working knowledge of quality control standard test/inspection tools, equipment, and sampling techniques/plans.
Supervisory Responsibilities:

N/A

Working Conditions:
  • Controlled area (Cleanroom) / Office environment
  • An applicant should not have any medical conditions that prevent accessing the controlled production area.
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