Quality Management Specialist

3 days ago


Konak, Turkey Maxwill International Full time

We are seeking a seasoned Quality Management Specialist to join our team at Maxwill International.

The ideal candidate will possess extensive experience in quality management systems and have a proven track record of ensuring compliance with regulatory requirements.

Below are the key responsibilities of this role:

  1. To establish, implement, and maintain a quality management system that aligns with the company's objectives.
  2. To conduct regular audits to ensure the operability of the quality management system across all departments.
  3. To develop and implement quality procedures and instructions, ensuring they are approved and effectively used by all staff members.
  4. To verify that measurement and inspection equipment is calibrated regularly to ensure product quality meets specified standards.
  5. To analyze quality control data on a periodic basis, identifying trends and areas for improvement.
  6. To manage the distribution and update of quality documents, preventing the reuse of obsolete materials.
  7. To initiate corrective actions when necessary, collaborating with other departments to address quality issues.
  8. To maintain records of calibration for quality control devices, adhering to established schedules.
  9. To participate in supplier evaluations and foster relationships with external organizations related to quality assurance.
  10. To lead internal audit teams, prepare annual audit plans, and ensure continuous communication of results.
  11. To promote occupational health and safety awareness among employees, ensuring adherence to relevant regulations.
  12. To take swift action to resolve non-compliance issues with medical devices and products supplied to the market.

The successful candidate will possess:

  • A bachelor's degree in a relevant field.
  • A minimum of 12 years of experience in quality management, with team leadership skills.
  • Advanced English language proficiency (written and spoken).
  • Familiarity with Microsoft Office and Logos software.
  • Knowledge of MDR, MDD processes, and FDA regulations.
  • Mastery of ISO 13485 certification processes.
  • Strong analytical thinking, problem-solving, and time management skills.

This position offers a challenging opportunity for a motivated professional to make a significant impact at Maxwill International.



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