Quality Control Inspector
Job in
Jeddah, Saudi Arabia
Listed on 2026-06-04
Listing for:
Tamer Mölnlycke Care
Full Time
position Listed on 2026-06-04
Job specializations:
-
Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager -
Manufacturing / Production
QA Specialist / Manager
Job Description & How to Apply Below
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.
Responsibilities1. 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 streamline nonconformities.
- Perform in-process checks during production as per approved procedures
- Verify assembly and packaging compliance against specifications and work instructions
- Identify deviations and expedite escalation through the defined nonconformance process.
- Perform final inspection post-production 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.
- Conduct random product audits on trays and finished goods as per plan
- Document findings and forward identified nonconformities.
- Record inspection results in ERP to support traceability and batch history
- Maintain inspection records in compliance with Good Documentation Practice (GDP).
- Monitor production compliance with approved procedures and work instructions
- Escalate GMP deviations immediately to Quality Operations Manager or assigned supervisor.
- Diploma or bachelor’s degree in engineering, Life Sciences, or related field
- 0–1 years experience in manufacturing inspection or quality-related roles (medical device preferred)
- Exposure to in-process and final inspection activities is preferred
- ERP inspection entries (basic)
- MS Office (basic)
- eQMS familiarity (preferred)
- English (fluent)
- Arabic (preferred)
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