Process Scientist II

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Process Scientist II

Published on:
Jan 28, 2026

Country:
United States

Job Category:
Operations

Employment type:

Regular Full Time

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the 'Diagnostics Specialist.'

Why Join Diasorin? Impactful Work:
When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach &

Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture:
We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team:
If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare.

Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!

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 Responsibilites

• 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.
• 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.
• 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.
• 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 Smart Train 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…