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Process Validation Engineer with medical domain

Diverse Lynx, LLC

Northridge, CA

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JOB DETAILS
SKILLS
Assembly Line, Biomedicine, Code of Federal Regulations, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Electrochemistry, External Audit, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), ISO (International Organization for Standardization), Internal Audit, Maintain Compliance, Manufacturing, Manufacturing Engineering, Manufacturing Operations, Manufacturing Requirements, Manufacturing/Industrial Processes, Medical Diagnosis, Medical Equipment, Minitab, Process Capability, Process Engineering, Process Improvement, Process Validation, Regulations, Risk Analysis, Root Cause Analysis, Semiconductors, Six Sigma Black Belt, Six Sigma Green Belt, Statistical Modeling, United States Department of Energy (DOE), Validation Documentation, Validation Plan, Wafer Manufacturing
LOCATION
Northridge, CA
POSTED
7 days ago

JD:

  • Develop and execute IQ/OQ/PQ protocols for critical manufacturing processes.
  • Conduct process characterization using DOE, SPC, and statistical modeling.
  • Perform process capability studies (Cp/Cpk) and implement corrective actions for low‐capability processes.
  • Define and maintain the Process Validation Master Plan (PVMP).
  • Prepare validation protocols, reports, risk assessments, PFMEAs, and process maps.
  • Support pilot‐to‐production scale‐up for new blood glucose sensor manufacturing lines.
  • Optimize process parameters for yield, throughput, and quality.
  • Lead root‐cause analysis and CAPA activities related to process deviations or excursions.
  • Ensure compliance with FDA 21 CFR Part 820, ISO 13485, and GMP regulations.
  • Support internal, external, and regulatory audits by providing process validation documentation.
  • Work with Manufacturing Engineering and Operations to implement validated processes on the production floor.
  • Train technicians and operators on validated processes and control plans.

Required

  • Bachelor's degree in Biomedical, Chemical, Mechanical, Industrial, or related Engineering field.
  • 3+ years of experience in process validation within a medical device, diagnostics, or biosensor environment.
  • Strong knowledge of DOE, SPC, statistical tools (JMP/Minitab), and validation methodologies.
  • Understanding of regulated medical device manufacturing and QMS requirements.

Preferred

  • Experience with blood glucose sensor processes or electrochemical sensor manufacturing.
  • Six Sigma Green Belt or Black Belt certification.
  • Experience with automated or semi‐automated process lines.

Experience in the semiconductor industry for wafer production

Diverse Lynx LLC is an Equal Employment Opportunity employer. All qualified applicants will receive due consideration for employment without any discrimination. All applicants will be evaluated solely on the basis of their ability, competence and their proven capability to perform the functions outlined in the corresponding role. We promote and support a diverse workforce across all levels in the company.

About the Company

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Diverse Lynx, LLC