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 This position will be responsible for participating in the company's day to day Reasearch & Development activities which include design, execution and interpretation of scientific experiments and design and development of assays based on Luminex's technology platform and chemistries. Handles scientific experiments independently with minimal supervision. Key Duties and Responsibilities
Day-to-day "hands on" work in the laboratory including, planning and designing of experiments, generating, recording, and analyzing experimental data and maintaining laboratory notebooks. This involves working in Biosafety Level II laboratory with biological samples and nucleic acid extractions.
Routinely, assemble and present data to departmental, project, and cross-site teams
Significantly contribute to writing protocols and reports relating to feasibility, verification and validation of molecular tests under quality system requirements
Interface across the organization and work closely with other functional groups, such as, Quality Affairs, Regulatory Affairs, Clinical Affairs, Design Transfer, Manufacturing, and Quality Control regarding priorities and timetables for deliverables
Provide training and technical support to junior members of the team
Assist in intellectual property development
Conform to applicable Design Control regulations and standards
Troubleshoot technical difficulties, as required
Comply with the company quality policies and operating procedures
Participate in the maintenance of general laboratory organization
Performs other duties as assigned related to duties as assigned
Education, Experience, and Qualifications
Associate's Degree Community College 2-year diploma (technical) in biochemistry, biology, molecular biology, or a related scientific field combined with at least 5 years' laboratory work experience in molecular biology or the biotechnology industry required or
Bachelor's Degree Bachelor degree in biological/chemical or related scientific disciplines with 2 years relevant experience/training preferred or
Master's Degree Master's degree in biological/chemical or related scientific disciplines with no relevant experience/training preferred or
2+ Years Expertise in a variety of molecular and biochemical laboratory procedures required
2+ Years Knowledge of routine laboratory methods such as PCR, data analyses, specimen handling and processing, and experimental documentation required
2+ Years Working knowledge or experience with ISO 13485:2016 standards and FDA regulations preferred
2+ Years Prior medical device industry experience preferred
Excellent oral and written communication skills. (High proficiency)
Proficient in Microsoft Word, Excel, and PowerPoint programs. (High proficiency)
Highly organized with proven time management and prioritization skills (High proficiency)
Ability to work independently and with minimal supervision (High proficiency)
Ability to handle the pressure of meeting tight deadlines (High proficiency)
Excellent interpersonal skills with proven ability to work both in a team-oriented environment and independently (High proficiency)
Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (Medium proficiency)
Mathematics and statistics aptitude. (Medium proficiency)
Data analysis and technical writing aptitude. (Medium proficiency)
What we offer
Receive a competitive salary and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world.
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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 hr@diasorin.com.
Recruitment Fraud Notice
Diasorin never requests payment, financial information, or personal banking details from candidates at any stage of the recruitment process. Official communications from Diasorin recruiters will only come from a verified @diasorin.com email address. If you have questions about the legitimacy of a recruitment communication, please contact hr@diasorin.com for verification.
Unauthorized third-party recruiting agencies may not submit candidates for this position without prior written authorization from the Diasorin Human Resources Department.
DiaSorin
Mar 26, 2026