Process Scientist II

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 is responsible for material processing, reagent formulation, technical manufacturing, in-process and final quality control of reagents, components and in-vitro diagnostic products.

Job Responsibilities and Duties

• Perform material processing and reagent formulation for bulk intermediates and components.
• Determine reprocessing needs for calibrator, controls, and conjugates.
• Perform Good laboratory practices - maintain clean work space in QC and Reagent Prep labs. Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance.
• Utilize SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting, and flow through facility. Additionally, create and run reports and train others on the use of SAP.
• Participate in inventory accountability - PSA count, cycle counts, accurate kiting, etc.
• Perform in-process testing and final Quality Control for LIAISON products per established procedures using the LIAISON analyzer family.
• Analyze testing results of technical manufacturing, quality control, or product performance to determine acceptability of product relative to established requirements.
• Assign calibrator values to optimize kit performance.
• Assign kit control ranges per established procedures.
• Monitor internal control supplies and manufacture new controls as needed.
• Assign internal controls using bias methods to ensure consistent kit performance.
• Perform second-checking to ensure accurate records.
• Perform trending of internal controls and other critical to quality specifications for assigned products to ensure proper performance of kit and controls.
• Follow regulatory requirements - follow document instructions and maintain reasonable documentation error rates.
• Ensure proper documentation by:
• Correcting errors noted in procedures and forms
• Ensuring proper documentation by creating new documents and making significant revisions to current documentation for process changes, clarity or consistency.
• Perform tasks assigned in NCR / Deviations and Validations.
• Perform tasks assigned in CAPA.
• Write NCR / Deviations.
• Write and execute Validation Plans and Reports.
• Perform Risk Assessments.
• Ensure safety of self and others by complying with all company safety policies, including use of PPE.
• Participate in team meetings and attend group training sessions.
• Monitor training required in SmartTrain and ensure timely completion of all company training requirements.
• Help with basic new employee training such as instrument use, basic software training, etc..
• Help with intermediate level employee training such as more complex QC processes and assignment of controls, calibrators, etc.
• Contribute to business continuity or continuous improvement projects by:
• Suggesting improvements and completing assigned tasks.
• Executing investigations where needed, defining project/scope and writing quality plans and/or validation plans.
• Complete assigned tasks related to investigations for root cause determination and troubleshoot product or process issues.
• Execute investigations for root cause determination and troubleshoot product or process issues.

Education, Experience and Qualifications

• Bachelor's Degree or Master's degree in Chemistry, Biology, Medical Technology or related science field or a 2 year degree (i.e. MLT) with equivalent experience Required
• 3+ Years of related laboratory experience and/or demonstrated competence within the in-vitro diagnostic industry Required
• Basic understanding of immunology and immunoassay techniques
• Ability to work in a regulated environment
• Working knowledge of:
• General lab equipment (e.g. pH meter, balances, mixers, etc.)
• MS Excel, familiar with Google Suite
• Ability to work with minimal supervision
• Knowledge of statistical analysis and reporting methods
• Ability to train team members on basic group procedures and tasks
• Advanced skills in mathematical and calculations, writing and documentation skills, analytical skills, and ability to grasp complex concepts and solutions.
• Correctable Vision (inspection work) and Ability to Distinguish Color (Label Inspection) required.

What we offer

The hiring range for this position is $70,000 – $85,400 annually. The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance.

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.