Scientist, Product Transfer II

About Diasorin

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."

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!

This position is responsible for Product Transfer activities including creation of formulation documentation, implementation of quality control procedures, validation reagent formulation including quality control and support of products post launch within the LIAISON Reagents department.

• Work in conjunction with Product Development in creation of all documentation for LIAISON® Reagent Manufacturing and Quality Control for new products. Create part numbers for new products in the design cycle.
• Create routings for new part numbers created in design cycle.
• Aid in creation of part numbers and routings for newer team members.
• Manufacture new Internal Controls for product in the design cycle.
• Serve on Core Teams for assigned development projects.
• Perform material processing and reagent formulation for bulk intermediates and components.
• Determine reprocessing need for calibrator, controls and conjugates, with assistance.
• Maintain clean work space in QC and Reagent Prep labs, consistent with Good Laboratory Practices (GMP).
• Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance.
• Utilize basic SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting and flow through facility.
• Participate in inventory accountability - PSA count, cycle counts, accurate kitting, etc.
• Perform in‑process testing and final QC 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, with assistance.
• Perform second‑checking to ensure accurate records.
• Follow regulatory requirements – follow document instructions and maintain reasonable documentation error rates.
• Ensure proper documentation by correcting errors noted in procedures and forms.
• Ensure 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.
• E…