REACH​/CLP Product Compliance Senior Specialist

Location: Saluggia

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

The EHS Product Compliance Senior Specialist is responsible for ensuring chemical regulatory compliance of Diasorin diagnostic kits, with particular reference to Safety Data Sheets (SDS), safety labels, and related documentation.

The role ensures that applicable regulatory requirements (including REACH, CLP, and GHS) are properly interpreted and implemented, guaranteeing product compliance throughout the entire lifecycle and across different target markets.

The position operates in an international context, contributing to the definition and implementation of global standards for SDS and labeling, and supporting Immuno platform sites in ensuring their consistent adoption.

The role collaborates with key company functions (R&D, Quality Assurance, Regulatory Affairs, Manufacturing) to ensure a coordinated and consistent approach to chemical safety management and product compliance.

Key Duties And Responsibilities

Draft, review, and update Safety Data Sheets (SDS/MSDS) for Diasorin diagnostic kits and reagents, ensuring full compliance with REACH, CLP, and GHS regulations, as well as applicable national and international requirements.

Ensure regulatory consistency and global harmonization of SDS and product documentation across target markets (EU and non‑EU), contributing to the definition of common standards and templates, and supporting Immuno division sites in their correct and consistent implementation.

Prepare, maintain, and update regulatory documentation supporting diagnostic kits (e.g., SDS, IFU, labels, declarations of conformity), ensuring full compliance of safety labeling (IVDR, CLP/GHS) and consistency among SDS, IFU, and labeling across different markets.

Manage and maintain dossiers of chemical substances used in products, including registration, notification, and communication activities with ECHA and other Competent Authorities, where required.

Act as the company’s technical-regulatory reference for chemical safety and product compliance topics.

Proactively monitor regulatory developments (e.g., REACH, CLP, SVHC, PFAS, POPs, RoHS), assess their impact on products, and promptly implement necessary updates to technical and regulatory documentation using a risk-based approach.

Contribute to the definition, implementation, and continuous improvement of company processes related to the management of SDS and product regulatory documentation.

Contribute to monitoring compliance and harmonization performance (e.g., SDS updates, labeling alignment, audit outcomes), supporting continuous process improvement.

Collaborate with R&D, Quality Assurance, Regulatory Affairs, Manufacturing, and Marketing to collect, verify, and manage technical and safety information throughout the entire product lifecycle.

Provide specialist support during internal audits, certification audits, and Authority inspections, ensuring the availability and traceability of required…