Saim Technologies

11 jobs near Columbus, OH

Position: Equipment engineer Location: Northridge, CA Type: long term contract Position summary: Key Responsibilities * Develop and execute Installation, Operational, and Performance Qualification ...

EquipmentEngineer

Los Angeles, CA ยท On-site

$93K - $119K/yr

Position : Equipment Engineer Location Northridge, CA-On Site Duration: Long Term Contract Key Responsibilities * Develop and execute Installation, Operational, and Performance Qualification (IQ/OQ ...

Job Title: Supplier Quality Engineer Location: Irvine, CA or Salt Lake City, UT (Onsite) Position Summary: Supplier Quality Engineer is responsible for ensuring suppliers deliver quality materials ...

Equipment engineer

Saim Technologies

Los Angeles, CA โ€ข On-site

Other

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Position: Equipment engineer

Location: Northridge, CA

Type: long term contract

Position summary:

Key Responsibilities

  • Develop and execute Installation, Operational, and Performance Qualification (IQ/OQ/PQ) protocols specifically for blood glucose monitoring sensor manufacturing equipment.
  • Define and document critical process parameters (CPPs) and equipment capabilities to ensure stable sensor performance within specification limits.
  • Establish preventive maintenance plans, calibration schedules, and critical spare parts lists.
  • Author validation plans, validation protocols, test reports, including deviations and corrective actions and Standard Operating Procedures (SOPs).
  • Utilize tools such as Minitab to analyze large datasets from sensor builds, performing Design of Experiments (DOE) and process capability studies.
  • Perform equipment risk assessments, including pFMEA and hazard analysis.
  • Define User Requirements Specifications (URS) for new equipment and lead equipment installation and commissioning efforts.
  • Train technicians and operators on validated equipment procedures.
  • Ensure compliance with FDA 21 CFR Part 820, ISO 13485, and GMP regulations.
  • Partner with R&D, Quality Assurance, and external vendors to scale up pilot lines to highvolume production.
  • Work with Manufacturing Engineers to improve equipment reliability and throughput.
  • Support internal and external audits by providing equipment validation evidence.

Required Qualifications

  • Bachelor s degree in mechanical, Electrical, Industrial, Biomedical Engineering, or a related field.
  • 3+ years of equipment validation experience within medical device manufacturing.
  • Strong understanding of GMP, GAMP 5, and FDA equipment validation requirements.
  • Familiarity with automated equipment, robotics, PLCs, and machine vision systems.

Preferred Qualifications

  • Prior experience validating equipment for biosensor or electrochemical sensor manufacturing, or experience in the semiconductor industry for wafer production.
  • Experience with highspeed automation and semiautomated production lines.
  • Certification in equipment validation or GAMP 5 training.