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.
Numbers & Facts
Location
Northridge, CA
Skills
Assembly Lineunmatched
Biomedicineunmatched
Code of Federal Regulationsunmatched
Corrective Actionunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Electrochemistryunmatched
External Auditunmatched
FDA (Food and Drug Administration)unmatched
GMP (Good Manufacturing Practices)unmatched
ISO (International Organization for Standardization)unmatched
Internal Auditunmatched
Maintain Complianceunmatched
Manufacturingunmatched
Manufacturing Engineeringunmatched
Manufacturing Operationsunmatched
Manufacturing Requirementsunmatched
Manufacturing/Industrial Processesunmatched
Medical Diagnosisunmatched
Medical Equipmentunmatched
Minitabunmatched
Process Capabilityunmatched
Process Engineeringunmatched
Process Improvementunmatched
Process Validationunmatched
Regulationsunmatched
Risk Analysisunmatched
Root Cause Analysisunmatched
Semiconductorsunmatched
Six Sigma Black Beltunmatched
Six Sigma Green Beltunmatched
Statistical Modelingunmatched
United States Department of Energy (DOE)unmatched
Validation Documentationunmatched
Validation Planunmatched
Wafer Manufacturingunmatched
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