Quality Assurance Specialist

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7goaej

We are a global developer and manufacturer of interventional medical devices in the fields of endovascular and interventional cardiology. We manufacture our products entirely in-house, from raw materials to finished goods, and distribute them worldwide through our direct sales force and network of distributors.

We are looking for a tempo pieno QA Specialist for our Italian headquarters to join an already structured team.

Role Purpose:

Reporting directly to the QA Manager , you will play a key role in maintaining and improving the Quality Management System, ensuring compliance with ISO 13485 and EU MDR 2017⁄745 . You will collaborate closely with cross-functional teams to support quality processes and regulatory requirements.

Key Responsibilities

- Support the preparation, revision, implementation, and release of Quality Management System procedures.
- Participate in internal and external auditing activities.
- Manage Product Change Control and CAPA (Corrective and Preventive Actions) processes.
- Prepare validation protocols and reports for cleanroom qualification and validation activities.
- Support the QA Manager with Quality System activities, including the preparation of Management Reviews .
- Perform trend analyses in collaboration with the Clinical team to support complaint management.
- Prepare and maintain usability documentation.




- Contribute to the integration and continuous improvement of Quality System documentation to ensure compliance with EU MDR 2017⁄745 .

Qualifications

- Bachelor’s degree or equivalent background in a relevant scientific or technical field.
- At least 3 years of experience in a Quality Assurance role within a structured organization, preferably in the medical device or another regulated industry.
- Good knowledge of ISO 13485 and EU MDR 2017⁄745 .
- Understanding of Quality Management Systems and auditing processes.
- Experience participating in internal and/or external audits.
- Fluent English (written and spoken).
- Auditor certification is considered a strong advantage.

Soft Skills

- Strong organizational skills
- Accuracy and attention to detail
- Flexibility and adaptability
- Problem-solving mindset
- Results-oriented approach
- Excellent communication and teamwork skills

What We Offer

- Location: CID S.p.A., Via Crescentino SNC, 13040 Saluggia (VC), Italy
- Compensation: Level between D1 and C2 of the “Industria-Chimica” CCNL - with a RAL ranging between 34.000€ & 36.000€

Equal Opportunity Employer

This position is open to candidates of all genders, in accordance with Italian Laws 903⁄77 and 125⁄91 , and to candidates of all ages and nationalities, pursuant to Legislative Decrees 215⁄03 and 216⁄03 .

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7goaej