Monitor the implementation of Design Controls in the development projects.
Help in generating and maintaining DHF records.
Help in managing the products Technical Documentation.
Approve suppliers and maintain the records of supplier certification.
Perform impact assessment on ECOs.
Handling the non-conformance process.
Handling the CAPA system.
Perform incoming inspections for new assets.
Manage the DMR.
Help in assuring the QMS compliance with all applicable standards and regulations.
Responsibility for Internal Audits planning. Monitor Internal audits execution.
Handling customer complaints.
Help in generating and maintaining DHF records.
Help in managing the products Technical Documentation.
Approve suppliers and maintain the records of supplier certification.
Perform impact assessment on ECOs.
Handling the non-conformance process.
Handling the CAPA system.
Perform incoming inspections for new assets.
Manage the DMR.
Help in assuring the QMS compliance with all applicable standards and regulations.
Responsibility for Internal Audits planning. Monitor Internal audits execution.
Handling customer complaints.
Requirements:
Experience in quality management systems for medical devices.
Ability to work in a collaborative environment.
A passion for leveraging technology to improve patient outcomes.
Certification as a Quality engineer or an academic degree in science or engineering
English – Fluent.
Experience in quality management systems for medical devices.
Ability to work in a collaborative environment.
A passion for leveraging technology to improve patient outcomes.
Certification as a Quality engineer or an academic degree in science or engineering
English – Fluent.
This position is open to all candidates.
