Quality System Specialist

Diasorin; Saluggia; On-site; EUR 34,000 - 38,000; Full time

Benefits offered by this job

Free canteen

Well-being program: Feel Good - Diasor

Supplementary pension fund

Job summary

Diasorin is seeking a Diagnostics Specialist to advance quality management systems in line with medical device and IVD regulatory requirements. You will drive documentation, trainings, and audits to ensure compliance across subsidiaries and customers.

The role requires a degree in scientific/technical disciplines, 1+ year in pharma/medical devices, and fluent English, with strong communication and problem-solving skills. Permanent contract in Italy with competitive base salary and benefits.

Qualifications

• Degree in scientific or technical disciplines.
• At least one year experience in similar roles in chemical/pharma or medical device industries.
• Familiarity with Office programs (Excel, PowerPoint, Word).
• Strong verbal and written communication skills.
• Fluent English language.

Responsibilities

• Develop and maintain a Quality management system in line with regulatory requirements (ISO 9001, ISO 13485, cGMP, IVDR).
• Update and control documentation per QMS.
• Promote QMS awareness across all levels of the company.

Skills

Quality focus

English fluent

Analytical skills

Communication skills

Teamwork

Education

Degree in scientific/technical disciplines

Tools

Microsoft Office (Excel/PowerPoint/Word)

Job description

Obsessed by Science. Entrepreneurial by Nature. United by Purpose.

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.

As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry’s broadest specialty diagnostic portfolios.

When you join Diasorin, you are not just filling a role. You are helping build what comes next.

Why Join Diasorin

• Build What Matters Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.
• Innovate with Agility at a Global Scale Work in an entrepreneurial environment that enables speed, collaboration, and global impact.
• Grow in a People-Centered Culture Thrive in a culture that values accountability, inclusion, and continuous development.

Job Scope

• Develop and maintain a Quality management system in line with the regulatory and mandatory requirements applicable to Medical Device and IVD (including ISO 9001, ISO 13485, cGMP, IVDR ecc) through existing and new documentation
• Ensure that all relevant documents are updated, revised and modified in accordance with quality management system requirements
• Spreads awareness of quality management system to all levels of the company
• Spread, through appropriate trainings, a culture of continuous improvement and good manufacturing practice across the company
• Cooperate with other functions to ensure that new projects and processes are in compliance with all internal and external requirements.
• Determine, through planned internal audits, whether the Quality management system is conform to the applicable requirements and effectively implemented and maintained
• Support Subsidiaries, Distributors and customers providing required product documentation

Key Duties And Responsibilities

• Ensure that all relevant documents are updated, revised and modified in accordance with quality management system requirements
• Ensure that changes inside DSI are evaluated and managed in accordance with quality management system requirements
• Support Product Development dept providing documentation for new products
• Support the Regulatory dept providing documentation in compliance with the needs of external certification bodies
• In company quality projects ensure that all activities are performed in compliance with quality a system requirements
• Ensure that training activities are managed and recorded according to the quality requirement in order to give evidence that personnel is adequately trained for a specific job.
• Perform training personnel about the requirements of QMS and cGMP.
• Manage internal audit ensuring that they are performed at regular intervals and that all nonconformities raised during audits are effectively corrected
• Give support to second and third party audits
• Provide product documentation (i.e certificates od Analysis, certificate of cornformance, ISO certificate ecc…) upon customer requests or for commercial purposes

Education, Experience, And Qualifications

• Degree in scientific or technical disciplines.
• At least one year experience in similar or equivalent positions in chemical/pharmaceutical or medical device industries, or experience in the production/quality control of medical devices.
• Familiarity with Office programs such as Excel, PowerPoint, and Word
• Strong verbal and written communication skills
• Solid problem solving and analytical skillsSolid interpersonal skills, including ability to negotiate and influence without authority
• Strong communication and interpersonal skills with ability to work well in a high pressure environment
• Strong competency in Customer Focus and Driving for Results
• Fluent knowledge of the English language

What We Offer

• Permanent employment contract
• Classification under the Chemical-Pharmaceutical CCNL (Italian national collective bargaining agreement)
• Gross annual base salary from € 33.598,46
• Variable compensation linked to the achievement of objectives
• Actual pay is set on objective criteria: seniority, distinctive skills, scope of responsibility.

At Diasorin, we are committed to supporting the well-being of our employees every day - which is why we complement compensation with a comprehensive set of benefits:

• Free canteen
• Feel Good - Diasorin for You: a dedicated well-being program offering initiatives, services, and opportunities designed to support you every day
• A benefits package guaranteed by the Chemical-Pharmaceutical CCNL, including a supplementary pension fund and supplementary healthcare coverage
• Company welfare plan offering flexible benefits you can tailor to your needs

Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide.

Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law.

This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction.

Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process. If assistance is required, please contact [e-mail].