
Fujifilm
Santa Ana, California • Today
Full-time
USD 106,185.25 - 115,000.00 per year
19 results (1 new)

Fujifilm
Santa Ana, California • Today
Full-time
USD 106,185.25 - 115,000.00 per year

Katalyst Healthcares and Lifesciences
Remote or Boston, Massachusetts • Today
Full-time

M/A-COM Technology Solutions Inc
Newport Beach, California • Today
Full-time
USD 84,000.00 - 166,000.00 per year

Rivian
Irvine, California • Today
Full-time
USD 85,400.00 - 94,900.00 per year

Katalyst Healthcares and Lifesciences
Remote or San Francisco, California • Today
Full-time

Katalyst Healthcares and Lifesciences
Remote or Springfield, Massachusetts • Today
Full-time

Katalyst Healthcares and Lifesciences
Remote or Minneapolis, Minnesota • Today
Full-time

Katalyst Healthcares and Lifesciences
Remote or Salt Lake City, Utah • Today
Full-time

Katalyst Healthcares and Lifesciences
Remote or Rock Hill, South Carolina • Today
Full-time

Katalyst Healthcares and Lifesciences
Remote or Evansville, Indiana • Today
Full-time

Katalyst Healthcares and Lifesciences
Remote or Massachusetts • Today
Full-time

Katalyst Healthcares and Lifesciences
Remote or Bothell, Washington • Today
Full-time

Katalyst Healthcares and Lifesciences
Remote or Raleigh, North Carolina • Today
Full-time

🔗 Matching skills to job...
Irvine, California
•
29d ago
Job DescriptionMust Have Technical/Functional Skills 5+ years of hands-on testing experience in medical device or regulated industry Strong experience in: Executing IQ/OQ/PQ protocols, Protocol reading and step-by-step execution, Test data recording and documentation Familiarity with: Lab instruments (multimeters, oscilloscopes, sensors, etc.), Equipment validation processes Understanding of GxP and validation practices Experience with Veritas Console or similar medical equipment Exposure to equ
Easy Apply
Full-time
100,000 - 110,000
Los Angeles, California
•
Today
Position: Equipment EngineerLocation Northridge, CA-On SiteDuration: Long Term Contract Key ResponsibilitiesDevelop 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
Easy Apply
Third Party, Contract
$60+
Remote or New Jersey
•
Today
Job Description: We are seeking a Computer System Validation (CSV) Engineer with experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical or biotechnology environment. The ideal candidate will have expertise in GAMP 5, 21 CFR Part 11, validation lifecycle documentation, and QC laboratory or manufacturing systems validation, while collaborating with cross-functional teams to ensure regulatory compliance. Roles & Responsibilities: Develop, execute, and maintain Computer
Full-time
No location provided
•
Today
Direct hire /Full time On-site Boulder, CO Salary expectation: You povide Summary We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The successful candidate will lead and execute CQV deliverables associated with GMP-regulated process equipment, utilities, automation systems, cleanrooms, and manufacturing operations. This role requires hands-on technical expertis
Easy Apply
Full-time
$DOE