Quality Assurance Supervisor

Farir Asa Teb Pardis

Posted 10 months ago

Job Description

  • Prepare and complete quality documentation, meet professional QA objectives provide reports on a regular basis, and have experience in self-inspections internal and external audits.
  • Develop, periodically review, revise, and implement SOPs and other documents needed in different processes.
  • Assist in the investigation process and define optimized process work.
  • Follow priorities in order to implement corrective and preventive actions.
  • Quality risk management.
  • Apply CAPAs or change management.
  • Participate in corporate meetings to support strategies, for meeting changing regulatory requirements and driving projects across the operations to implement required changes efficiently and effectively.
  • Apply and ensure implementation of standardized operating procedures.
  • Approve documents according to templates and required GMPs, ISO IMS (ISO 9001:2015, ISO 13485:2016), etc.
  • Assess audit findings.
  • Provide inspectors with clear and comprehensive files (external audits).
  • Respond with proficiency to questions from inspectors (external and internal audits).
  • Periodic GMP and ISO13485:2016 training for relevant staff.
  • Analyze, monitor, and ensure that the organization's processes comply with international standards.

Requirements

  • 5 years of experience in a similar position.
  • Experience in the pharmaceutical or medical equipment industry.
  • Working knowledge of relevant GMP, ISO 13485:2016 guidelines and regulations.
  • Familiar with risk management methods.
  • Bachelor's or Master's degree in Industrial Engineering or Industrial Management.

Employment Type

  • Full Time

Details

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