Quality Management System Support - Bussolengo, Italia - Orthofix

Orthofix

Azienda verificata

Bussolengo, Italia

3 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

We offer an interesting opportunity to join our Quality Management System team, based in Bussolengo (VR) a Quality Management System Support, reporting to the Quality Management System Supervisor.

You will be part of Quality Team and it contributes to maintain live and in compliance the Quality Management System implemented in European Subsidiaries.

You will ensure that the OF Quality System conforms with all reference standards and regulatory requirements (ISO 13485, 21 CFR 820 ) and that supplied products are fit for their purpose and meet customer expectations.

QMSS co-ordinates the activities required to fulfill this aim.

Moreover, the QMSS monitors and reports on how the quality management system is performing and publishes data and reports regarding company performance against set indicators.

QMSS liaises with managers and staff internally to ensure the proper functioning of the Quality system.

Where appropriate, the QMSS reports on amendments and implements any changes required, and provides training, tools, and techniques to ensure that quality standards are maintained and can be achieved by all competent staff.

As maintaining quality demands continuously adapting to meet customer expectations, QMSS must place quality assurance at the heart of his/her responsibilities within the Company.

What will your contribution be?

Support QMS manager to ensure the maintenance of Quality Management System in compliance with applicable standards.
Ensure the maintenance of Quality Management System in European Subsidiaries.
Support QMS manager to ensure that all the Company processes are designed and executed according to policies, predetermined internal procedures and international applicable standards such as MDD, MDR, FDA or those of other Bodies; implement Best Practices and plan for continuous Quality System improvements projects with specific deployed tasks.
Maintain the adequacy of QMS Procedures and Operative Procedures, and that these are observed by all employees in the designated Group Companies.
Support QMS manager to define and document Quality specifications.
Interfunctional support to implement and formalize the design change and all other Quality modifications introduced in the Organization.
Coordinate the management of product modifications in cooperation with Organization.
Ensure quality trainings on new hires and for trainable documents.
Support QMS manager to coordinate and promote, define, achieve, and maintain the Quality Objectives in collaboration with the Management and with all departments.
Define and maintain the designated Group Companies' QMS and relevant documentation (including QM, SOPs, DHF, Traceability records, etc;)
Support QMS manager to address third party audits.
Support QMS manager to collect, evaluate and analyze Quality records, report periodically to management on quality issues, trends and losses.
Evaluate the Quality results achieved and notify to QMS manager any incompatibility with company objectives;
Promote internal training on quality matters in cooperation with all other functions;
Promotion and participation in continuous (breakthrough) processes
Support QMS manager to develop and implement Quality Policies and procedures with regards to the definition of the International applicable standards

What are we looking for?

Degree or master's degree
2 years in similar positions, in multinational companies preferably operating in the Medical Device field.
Fluency in English
Good knowledge of Microsoft Office

What soft skills will you improve?
- critical thinking.