QA industrial compliance specialist

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
Through the Quality Assurance function: to ensure that the industrial activities are fit for purpose, consistent and meet all internal and external requirements.

to ensure the adequacy and updating of Quality System with respect to the regulatory and quality requirements

to ensure labeling, IFU and any related documentation (e.g. changes, SOPs, specifications, attachments, etc.) are in compliance with the regulatory requirements

Key Duties And Responsibilities

to verify the application of the Quality Management System

to draft and review of standard operative procedures

to elevate to the line manager risks associated to his/her activities that could impact the QMS

to verify that procedures are properly established and applied to prevent non-conformity

to collaborate with the technical teams in the definition of the correct risk assessment on the product/processes

to support industrial departments in the process of requesting and applying the relevant Change

to evaluate the impact of the proposed Changes on its own field of competence

to manage the documentation to release the manufactured lots

to perform internal and external audits (in presence of appropriate certification)

to collaborate during audits conducted by external bodies to manage properly the team

to collaborate during internal audits

to support the correct process of review and release of labeling documents

to support the correct process of review and release of quality system documentation

to define actions for continuous improvement

Education, Experience, And Qualifications

Degree in scientific disciplines such as (but not limited to) Chemistry, Pharmacy, Biology,

or other professional qualification with previous experience in similar jobs.

At least 2 year of Medical Device-IVD or chemical-pharmaceutical industry experience in similar position

Knowledge of quality and compliance management as well as GMP requirements and, as plus, requirements applicable to In Vitro Diagnostic Medical Devices.

Knowledge of the main current requirements applicable to IVD field. Use of Office pack. Risk management and related tools.

Strong verbal and written communication skills

Solid problem solving and analytical skills

Strong communication and interpersonal skills with ability to work well in a high pressure environment

Strong competency in Customer Focus and Driving for Results

Native Italian and fluent English

What We Offer

Permanent employment contract

Classification under the Chemical-Pharmaceutical CCNL (Italian national collective bargaining agreement)

Gross annual base salary from € 35.117,32

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