Manufacturing Engineer II: Process Innovator & Automation

DiaSorin S.p.A.

Cypress (CA)

On-site

USD 97,000 - 132,000

Full time

14 days+

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Benefits offered by this job

Health benefits
Retirement plan
Time off programs
Wellbeing support

Job summary

DiaSorin S.p.A. in Cypress, California seeks a Manufacturing Engineer II to evaluate and optimize manufacturing processes, write validations, and support FDA/ISO requirements. You will work with Production and Technical Support to improve reproducibility, reduce costs, and implement new technology across the plant.

The role involves leading validation/PCR efforts, coordinating process validations, and participating in audits while ensuring EHS compliance and continuous workflow improvements.

Qualifications

  • Bachelor's Degree in Mechanical, Electrical or Industrial Engineering.
  • 2+ years BS-related experience in IVD, medical, pharmaceutical, or related industry.
  • 1+ years MS-related experience in IVD, medical, pharmaceutical, or related industry.
  • ASQ Certified Quality Engineer preferred.
  • Ability to read, analyze and interpret technical instructions and regulations.
  • Ability to write reports and present information to groups of managers and customers.

Responsibilities

  • Identify and fix technical challenges to improve product reproducibility.
  • Improve production processes to reduce costs and scrap.
  • Research and purchase new manufacturing technology including automated equipment.
  • Lead validation and PCR efforts for new manufacturing technology and provide training.
  • Coordinate and supervise validations of processes and equipment.
  • Participate on cross-functional core teams for new products to represent Operations.
  • Support internal and external audits.
  • Maintain and increase workflow while adhering to EHS policies.

Education

Bachelor's Degree in Mechanical, Electrical or Industrial Engineering
2+ Years BS-related experience in IVD/medical/pharmaceutical
1+ Years MS-related experience in IVD/medical/pharmaceutical
ASQ Certified Quality Engineer

Job description

DiaSorin S.p.A. in Cypress, California seeks a Manufacturing Engineer II to evaluate and optimize manufacturing processes, write validations, and support FDA/ISO requirements. You will work with Production and Technical Support to improve reproducibility, reduce costs, and implement new technology across the plant.

The role involves leading validation/PCR efforts, coordinating process validations, and participating in audits while ensuring EHS compliance and continuous workflow improvements.

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