Engineer II, QC - Chemical Analyzers/ Analytical Instruments
Core
Strengthen quality frameworks and enable data-based decision-making in an analytical instrumentation manufacturing environment.
Role type
Quality Control Engineer II
Builds
Advanced spectroscopy instrumentation for research, materials science, energy, and industrial applications
Domain
Manufacturing / Quality Control / Analytical Instruments
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
root cause analysis, corrective action planning, data analysis, quality documentation, process validation, equipment qualification, supplier quality management, regulatory compliance (ISO/GMP), Lean methodologies, SPC, FMEA, mistake-proofing
Preferred skills
spectroscopy, Six Sigma, information management systems, regulatory standards (FDA/USP/EP)
Technologies
Microsoft Office
Responsibilities
Support manufacturing and R&D teams in resolving quality and process-related issues; Participate on NPI teams to ensure quality requirements are incorporated into product and process designs; Drive root cause investigations and corrective actions related to component, assembly, and process failures; Analyze manufacturing and quality data to identify trends, sources of variation, and opportunities for improvement; Develop and maintain quality documentation, procedures, inspection methods, and control plans; Promote the utilization of Lean methodologies and quality tools such as Kaizen, 5S, SPC, CAPA, FMEA, and mistake-proofing techniques; Support process validation, equipment qualification, and implementation of engineering changes; Partner with Manufacturing Engineering to improve process capability, reduce scrap and rework, and improve overall product reliability; Engage in supplier quality activities including corrective actions, nonconformance investigations, and first article inspections; Ensure compliance with applicable quality standards and regulatory requirements including ISO and GMP practices; Support audits, nonconformance investigations, and continuous improvement initiatives
Seniority
Mid-level IC