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Job Description
- Responsible for documents control distribution and withdraw the obsolete and invalid versions of standard operating procedures.
- Verify that the documentation system is in place and well maintained.
- Prepare the approved document list and prepare the document status on regular basis.
- File & archive the documents such as deviation reports, internal and external audit reports, complaints & recall reports.
- Responsible for security & accessibility of all documents available in QA [hard and soft copies].
- Share and conduct quality internal audits against ISO Certifications.
- Evaluate audit findings and implement appropriate corrective actions.
- Interpret and implement quality assurance standards to different departments.
- Sett/Draft quality assurance policies and procedures.
- Collect, compile and Analyze statistical quality data to identify areas for improvement in the quality system.
- Monitor risk management activities.
- Assure ongoing compliance with quality and industry regulatory requirements.
- Participate in the change management process to assure the products or services continue to meet customer requirements.
- Responsible for external audit coordination & support renewal of ISO certification.
Job Requirements
- Bachelor's degree preferably in Science or any related filed.
- 3-5 years’ experience in QA field.
- Medical devices experience is a must.
- Problem Solving/Analysis Skills.
- Decision Making Skills.
- Details -oriented.
- Communication Proficiency.
- Collaboration Skills.
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