JOB PURPOSE
- Ensure the continuity and compliance of defective product approval and registration practices according to PR-CS-002 Defective Procedure and Straumann AG QMS-CORP-000288 Compliant Management procedures.
MAIN DUTIES AND RESPONSIBILITIES
- Conduct work in accordance with the system established and implemented according to CE, ISO 9001, and ISO 13485 standards in line with quality policies and objectives.
- Ensure the continuity and compliance of defective product approval and registration practices according to PR-CS-002 Defective Procedure and Straumann AG QMS-CORP-000288 Compliant Management procedures.
- Evaluate free products sent, those to be received, and rejected defective products (price difference invoice issued) together with CRM, LS-20 Defective Product Tracking List (including count results in a 3-month period) and report to senior management monthly.
- Conduct defective product counts every 3 months using the blind counting method in accordance with PR-LO-003 Stock Counting Procedure and report to Finance & Operations Director and Quality Manager.
- Ensure control and registration processes in the unit are carried out by different personnel.
- Fulfill requirements and ensure the security of form and product storage and preservation in the defective department.
- Ensure coordination between Quality, Customer Services, and Stock units.
- Report developing nonconformities to the quality unit.
- Communicate with personnel and customers as needed.
- Provide customer and personnel training as needed.
- Inform related departments, personnel, and customers about possible changes in the process.
- Train and organize unit personnel.
- Conduct necessary correspondence with Straumann AG, organize and hold meetings.
- Report daily transactions to the Quality Manager.
- Act as a proxy for the complaint specialist when needed.
SKILLS, EXPERIENCE & KNOWLEDGE REQUIREMENTS
Education Level:
- University degree, preferably in Biomedical Engineering
Experience:
COMPETENCY REQUIREMENTS
CORE COMPETENCIES:
- Ability to manage a team, adapt to flexible working hours, make decisions, have proper diction, strong verbal and written communication skills, fit for teamwork, and able to take responsibility
TECHNICAL COMPETENCIES:
- Proficiency in SAP
- Proficiency in Microsoft Office Programs, knowledge of medical devices
- English proficiency
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.
Employment Type: Full Time
Alternative Locations: Turkey : Ankara
TravelPercentage: 0 - 20%
Requisition ID: 14086
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