Assay Transfer Team Technician Italy

DiaSorin; Piemonte; In loco; EUR 30.000 - 37.000; Tempo pieno

Vantaggi offerti da questo lavoro

Free canteen

Well-being program

Supplementary pension fund

Supplementary healthcare

Descrizione del lavoro

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. The Diagnostics Specialist role supports industrialization, validation, and technology transfer to ensure high-quality product delivery across sites.

You will collaborate in defining processes, perform QC testing, and contribute to continuous improvement initiatives in a fast-paced manufacturing environment, within a culture of ethics and accountability.

Competenze

• Higher diploma or university degree in technical-scientific field.
• Experience in biomedical/medical device sector preferred.
• Strong written and verbal communication and interpersonal skills.

Mansioni

• Perform manufacturing and QC immuno liaison tasks in GMP-compliant environment.
• Prepare validation batches and pilots per Quality Procedures.
• Assist in drafting industrialization documents and technology transfer activities.
• Support validation and data analysis for new products/processes.

Conoscenze

Good English knowledge

Written and verbal communication

Interpersonal and organizational

Formazione

Higher diploma or university degree in technical-scientific field

Strumenti

Microsoft Office

Descrizione del lavoro

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Published on: Sep 11, 2026

Job Category: Operations

Employment type: Regular Full Time

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

Perform laboratory activities inherent to the areas of Manufacturing and/or QC Immuno Liaison (pilot lot/batch preparation, immunometric testing, and performance evaluation), in compliance with Quality Procedures and applying GMP, interacting with other laboratories/units in an environment where equipment and spaces can be shared.

Collaborate in defining industrialization processes and give a support in guaranteeing the industrialization deliverables, mainly for:

• new products and/or processes;
• design change of current products;
• change of products/processes, raw materials already industrialized into Operations’ area without impact on immunometric performance perceived by the user or declared;
• technology transfer process from another Site to DSI or from DSI to another DiaSorin Production Site;
• innovation and new continuous improvement ideas;
• validation activities of equipments/processes.

Key Duties and Responsibilities

Ensure compliance with the Code of Ethics, the Quality Management System, the Company Policies and the Corporate Procedures.

Related to Industrialization of new products/processes and design change of current product:

• Performs preparation of validation batches and/or pilots, in compliance with Quality Procedures and applying GMP
• Performs immunometric QC testing, data tabulation, evaluation of results in order to assess immunometric performance, in compliance with Quality Procedures and applying GMP
• Supports in drafting industrialization documents

Related to Transfer of Technology projects:

• Collaborates and supports the project team regarding the activities and deliverables of transfer, according to the Inter-Site procedures, including the support for production and QC flow training, and any validation activities (in the case of Sending Units). Gives support for the implementation of product/process and performs the validation activities from production to release, in case DSI is the Receiving Site.

Related to validation activities (equipment, activities for BRM, product/process changes that have no impact on the performance perceived by the user or declared):

• Supports in data collection and validation planning;
• May deal with change management;
• Handles the preparation of any validation/pilot batches and/or their QC approval;
• Supports in change implementation and ensuring deliverables

Related to Innovation projects and new continuous improvement ideas:

• Supports the team in data collection and analysis;
• Supports the team in the submission and approval of a new idea;
• Supports the team in the implementation of approved new ideas.

Education, Experience, and Qualifications

• Higher diploma or university degree in technical-scientific field
• Experience in the role, gained in companies/laboratories in the biomedical sector, preferably in the Medical Device sector, or in hospital laboratories, is appreciated
• Chemical, biology, biotechnology and immunometric assay knowledge
• Microsoft Office package knowledge
• Basic statistics principles knowledge
• Good written and verbal communication skills
• Good interpersonal and organizational skills
• Good English knowledge

What we offer

• 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] .