Summary
Overview
Work history
Education
Skills
Certification
LANGUAGES
Accomplishments
SOCIAL ACTIVITIES
References
Timeline
Generic

Arshad Ahmed Khan

RIYAD,Saudi Arabia

Summary

Accomplished quality control specialist with extensive expertise in ISO 9001 and ISO 13485 compliance, GMP, and clean room control. Proven track record in calibration, validation, and supplier evaluation, complemented by strong skills in statistical quality analysis and non-conformance resolution. Adept at leading teams through effective supervision and training while ensuring meticulous documentation and reporting. Proficient in MS Word, Excel, PowerPoint, and quality documentation systems. Committed to enhancing operational efficiency through rigorous quality standards and continuous improvement initiatives.

Overview

16
16
years of professional experience
1
1
Certification

Work history

Quality Control Supervisor

Factory of Medical Rubber & Plastic Materials
Riyadh
2019.01 - 2026.04
  • Review, approve, and verify QC inspection and testing results.
  • Report non-conformances and represent QC in Corrective Action Requests (CAR)
  • Perform supplier assessment and evaluation for new suppliers.
  • Establish, verify, and keep product specifications.
  • Monitor product quality through continuous inspection and statistical analysis.
  • Supervise QC activities ensuring compliance with company policy and aims.
  • Ensure QC procedures, work instructions, and standards are updated and implemented.
  • Investigate customer complaints and contribute to root-cause analysis and corrective actions.
  • Prepare and give quality reports to department management.
  • Establish and verify hygiene and cleaning procedures.
  • Prepare and check routine clean room cleaning schedules.
  • Investigate clean room contamination with microbiologist.
  • Perform instrument calibration as per approved procedures.
  • Validate clean rooms in compliance with international standards.
  • Validate Gamma sterilization, routine dose audits, and ETO sterilization.
  • Monitor in-house Ethylene Oxide (ETO) sterilization.
  • Liaise with contract sterilizers to keep compliant sterilization processes.
  • Control and keep Bill of Material (BOM) files.
  • Create new material codes and amend existing ones upon request.
  • (Branch of United Medical Industry Co. Ltd) � Riyadh, KSA

Quality Control Supervisor

Saudi Korea Industrial Co. Ltd
Riyadh
2010.01 - 2018.01
  • Conduct complex testing and re-testing for abnormal results.
  • Perform continuous in-process inspections (visual and automated)
  • Inspect finished products at defined frequencies.
  • Verify copper tube appearance during mass production.
  • Ensure products meet customer specifications stored in quality databases.
  • Extensive experience in quality control operations, including the use of precision measuring instruments such as vernier calipers, micrometers, and measuring tapes, along with laboratory and testing equipment such as pH meters, viscometers, mechanical stability testing machines, and hydrometers to ensure compliance with quality standards.
  • Supervised quality control activities involving precision measurement and testing using vernier calipers, micrometers, pH meters, viscosity measurement instruments, mechanical stability machines, and hydrometers to maintain product quality and process consistency.
  • Perform equipment setup, calibration, and testing.
  • Prepare quality reports, analysis action reports, and countermeasures.
  • Maintain quality documentation and records.
  • Riyadh, KSA

Education

B. Ed -

M.A.K Azad College
Ibrahimpatnam

B.A. -

Maulana Azad National Urdu University

M.A. - Economics

Kakatiya University
Warangal

Skills

  • Quality Control Inspection & Testing
  • ISO 9001 & ISO 13485 Compliance
  • GMP & Clean Room Control
  • Calibration & Validation
  • Supplier Evaluation & Audits
  • Non-Conformance (NCR) & CAPA / CAR
  • Statistical Quality Analysis
  • Sterilization (EtO & Gamma)
  • Documentation & Reporting
  • Team Supervision & Training
  • MS Word, Excel, PowerPoint
  • Windows Operating Systems
  • Quality Documentation & Reporting Systems

Certification

  • ISO 9001 & ISO 13485:2016 – Medical Devices QMS Auditor / Lead Auditor (Completed: 19–23 June 2022)
  • Good Manufacturing Practice (GMP)
  • Internal Quality Auditing
  • Instruments Calibration & Validation
  • Clean Room Operation and Control

LANGUAGES

English
Fluent
Urdu
Native
Telugu
Fluent
Arabic
Fluent

Accomplishments

  • Conducted internal audits and supplier quality assessments, improving vendor quality performance by 20%.
  • Introduced corrective and preventive action (CAPA) processes, increasing overall product compliance and reducing customer complaints by 18%.
  • Supervised a team of 25+ QC inspectors, improving productivity by 20% via training programs and performance monitoring systems.
  • Developed and enforced compliance with ISO 9001 quality standards, resulting in successful external audits with zero major non-conformities.

SOCIAL ACTIVITIES

  • Active member of vocational guidance and career development programs in the local
  • Documentation & Reporting

References

References available upon request.

Timeline

Quality Control Supervisor

Factory of Medical Rubber & Plastic Materials
2019.01 - 2026.04

Quality Control Supervisor

Saudi Korea Industrial Co. Ltd
2010.01 - 2018.01

B. Ed -

M.A.K Azad College

B.A. -

Maulana Azad National Urdu University

M.A. - Economics

Kakatiya University
Arshad Ahmed Khan