- Cooperation in preparing and regular update of PDCA.
- Monitoring and measurement the quality objectives and KPIs.
- Gathering input data for management review, plan for related meetings and prepare the meeting note.
- Designing and documentation of business processes.
- Assuring process effectiveness throughout the organization by means of compliance with the international standards for management systems (e.g. ISO 9001, 13485, 10002).
- Handling all the related issues about non-conformities of departments.
- Preparing internal audit plan.
- Preparing checklist for internal audits.
- Implementation internal audits base on internal procedures and issuing related non-conformities.
- Follow up corrective actions and tracking effectiveness of them.
- Preparing internal audit report.
Requirements
- Degree in clinical laboratory science, clinical biochemistry, immunology or medicine and other related fields.
- At least 3 years useful work experience
- High level of competence with MS Office (Word, Excel, PowerPoint(.
- Knowledge of Quality Management Systems.
- Ability to gather and interpret information
- Ability to work under pressure and to deadlines.
- Ability to work both independently and as part of a team
- Ability to work with minimal supervision and ability to manage priorities and multi-tasking
- Excellent communication and presentation skills.
- Good team-working skills.
- Familiarity with Business Process Re-engineering is a must.
- Familiarity with time and motion study is a plus.
- Familiarity with medical devices standards is a plus
- Attributes: Result oriented, Systems thinking, fast responsive, Self-motivated.
- Work place: Karaj