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Production Lead Technician

Job in Cypress, Orange County, California, 90630, USA
Listing for: DiaSorin
Full Time position
Listed on 2026-06-13
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

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 Summary

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.

Key Responsibilities and Duties
  • 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 enhance product or business.
  • Review and revise existing documents. Able to recognize deficiencies and create new documents as required.
  • Inventory control – identify critical raw materials and establish and/or monitor a system to maintain control.
  • Able to support the design and execution of validation protocols and experiments to enhance product, resolve product issue, and manufacturing process. Contribute to lean manufacturing and continuous improvement projects as needed.
  • Close work orders and review manufacturing specification for accuracy and completeness.
  • Train new employees, monitor and provide feedback to employee and management…
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