Manufacturing Engineer II

Published on:
Oct 16, 2026

Country:
United States

Location:

Cypress, California

Job Category:
Operations

Employment type:

Regular Full Time

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.

Evaluate and optimize Manufacturing processes to improve product consistency, quality and to increase productivity. Write and perform validations and validation reports for production equipment as necessary. Support all applicable regulations including but not limited to FDA, ISO requirements.

• Work with Production and Technical Support personnel to identify, isolate and correct technical challenges for improving product reproducibility.
• Improve Production processes to reduce production costs and decrease scrap.
• Research and purchase new manufacturing technology including automated equipment to improve production using project management tools.
• Implement the transition of new manufacturing technology to ensure production continues successfully. This includes leading the validation and PCR effort as well as any training necessary.
• Coordinate and supervise required validations of processes and equipment.
• Improve and implement new processes.
• Participate on cross-functional core teams for new products to represent Operations and Manufacturing Engineering.
• Participate to support both internal and external audits.
• Maintain and increase work flow.
• Interact with all required departments to assist with project completion.
• Perform assigned tasks in accordance with applicable Environmental Health and Safety (EHS) regulations and Company EHS policies.
• May delegate and coordinate workload for technician group as needed. Responsible for enforcing all EHS policies in their span of control.
• Perform other duties as assigned.

• Bachelor's Degree in an engineering discipline such as Mechanical, Electrical or Industrial Engineering, Required
• 2+ Years with BS - related experience in IVD, medical, pharmaceutical, or other related industry, Required Or
• 1+ Years with MS- related experience in IVD, medical, pharmaceutical, or other related industry, Required
• ASQ Certified Quality Engineer, Preferred.
• Preferred understanding of statistical quality control, statistical process control, Corrective Action Process, and their application manufacturing as a problem identification and resolution tool
• Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
• Ability to write reports, business…