Production Lead Technician

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.

• 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.

Responsible for manufacturing and assembly of clinical and commercial products. Operates and troubleshoots production equipment. Manufactures product per documented manufacturing instructions. Maintains records to comply with GMP, SOP, quality system requirements, and other regulatory requirements. Performs in‑process testing to assure batches meet specifications. Works on complex assignments in a dynamic and fast paced environment where independent action and initiative are required to resolve problems.

Leads and develops manufacturing technicians. Supports all applicable regulations including but not limited to FDA, ISO, IVDD, and CMD/CAS requirements.

• Manufacture subassemblies, components, and/or kits per documented methods. Training requirements are listed in department specific TRQ.
• Perform in‑process testing of product, interpret results, and perform any required adjustments.
• Execute validation protocols and/or experiments.
• Investigate root causes of issues, identify and implement CAPA (Corrective Action and Preventative Action).
• Understand, comply, support, and enforce FDA and ISO regulatory requirements.
• Understand, comply, support, and enforce all policies and procedures.
• Perform lab maintenance per documented cleaning requirements.
• Maintain inventory, replenish raw materials and supplies as required.
• Store raw materials, subassemblies, components, and kits properly.
• Operate and maintain equipment per documented procedures, calibrate as required.
• Maintain product identification and traceability per SOP.
• Record required data on documents in accordance with GDP and SOP.
• Identify non‑conformances and initiate required documentation (NCMR, deviation report, CAPA, investigation report, risk assessments).
• Support leadership in reviewing and revising manufacturing specifications, department specific procedures, and creating new documents as required. Implement change via DCR.
• Recommend product or process improvements to enhance product or business.
• Review and revise existing documents; recognize deficiencies and create new documents as needed.
• Control inventory – identify critical raw materials and establish/monitor a system to maintain control.
• Support design and execution of validation protocols and experiments to enhance product, resolve issues, and improve manufacturing process. Contribute to lean manufacturing and continuous improvement projects as needed.
• Close work orders and review manufacturing specifications for accuracy and completeness.
• Train new employees, monitor and provide feedback to employees and management as required.
• Create and execute production schedule per plan; monitor progress of outstanding work orders and expedite as needed to meet scheduled due dates.
• Assist with special projects.
• Assist in other production areas/departments as needed.
• Write reports – investigations, risk assessments, validations, quality…