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Quality Control Inspector

Tamer Mölnlycke Care
Jeddah, KSA
Fulltime
Entry
2 months ago
Quality ControlQuality Assurance TestingTest StrategyDefect ManagementAgile MethodologiesSQL
Free

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Quality ControlQuality Assurance TestingTest Strategy
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Main Job Purpose

The Quality Control Inspector is responsible for performing inspection and verification activities during incoming material receipt, in-process control, assembly, packaging, and final inspection stages to ensure compliance with approved specifications, procedures, and Good Manufacturing Practice (GMP) requirements.

The role supports product conformity and batch disposition activities through accurate inspection execution, documentation, and timely escalation of nonconformities.

1. Incoming Inspection

  • Inspect incoming raw materials and components according to approved specifications and sampling plans
  • Verify documentation and identification status before acceptance
  • Accept or reject materials within defined inspection authority and escalate nonconformities.

2. In-Process Inspection (IPC)

  • Perform in-process checks during production as per approved procedures
  • Verify assembly and packaging compliance against specifications and work instructions
  • Identify deviations and escalate immediately through the defined nonconformance process.

3. Final Product Inspection

  • Perform final inspection postproduction and post sterilization (as applicable)
  • Verify labeling, packaging integrity, and required documentation completeness
  • Support batch disposition activities by ensuring inspection evidence is complete and traceable.

4. Product Audit Activities

  • Conduct random product audits on trays and finished goods as per plan
  • Document findings and escalate identified nonconformities.

5. Documentation & ERP

  • Record inspection results in ERP to support traceability and batch history
  • Maintain inspection records in compliance with Good Documentation Practice (GDP).

6- Gmp Compliance Monitoring

  • Monitor production compliance with approved procedures and work instructions
  • Escalate GMP deviations immediately to Quality Operations Manager or assigned supervisor.

Education

  • Diploma or bachelor’s degree in engineering, Life Sciences, or related field

Experience

  • 0–1 years experience in manufacturing inspection or quality-related roles (medical device preferred)
  • Exposure to in-process and final inspection activities is preferred

Computer Skills

  • ERP inspection entries (basic)

• MS Office (basic)

  • eQMS familiarity (preferred)

Languages

  • English (fluent)
  • Arabic (preferred)

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