The QA Specialist will be a part of the QA team and will be responsible for:
- Outline quality assurance policies and procedures
- Interpret and comply with quality assurance standards
- Oversee the implementation and ensure the efficiency of inspection and quality systems
- Plan, perform, and oversee inspection and testing of products to ensure the quality deliverable
- Document quality assurance activities, such as internal audits,,ECO,CAPA.
- Training: development and maintenance of quality training program.
- Labelling
Requirements:
- Minimum 3 years of QA experience in the medical device industry %28design control experience is an advantage%29
- At list BSc/BA in Bio-Medical/Mechanical/Biotechnology Engineering or Exact Sciences
- Strong written and verbal communication skills in English
- Excellent interpersonal skills, multitasking, and team player