Lead, Production Technician

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 have 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!

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's, SOP's, 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 of subassemblies, components, and/or kits per documented methods. Training requirements are listed in department specific TRQ (Training Requirements).
• In‑process testing of product with ability to interpret results and perform any required adjustments to product.
• Execute validation protocols and/or experiments.
• Ability to perform investigation to identify potential root cause of an issue. Ability to 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.
• Lab maintenance per documented cleaning requirements.
• Inventory maintenance, replenish raw materials and supplies as required.
• Proper storage of raw materials, subassemblies, components, and kits.
• Equipment operation and maintenance per documented procedures, calibrate as required.
• Maintain product identification and traceability per Standard Operating Procedures (SOP).
• Record required data on documents in accordance with GDP (Good Documentation Procedures) and SOP.
• Identify non‑conformances and initiate required documentation. Documentation may include NCMR (Non‑Conforming Material Report), deviation report, CAPA, investigation report, and/or risk assessments.
• Support leadership with reviewing and revising manufacturing specifications, department specific procedures, and/or create new documents as required. Implement change via DCR (Document Change Request).
• Recommend to Supervisor/Manager product or process improvements which will…