Veronica Strong Email & Phone Number

Irvine, Ca, Us

Irvine, Ca, Us

Paris, Île-De-France, Fr

Irvine, California, Us

Laguna Hills, California/San Diego, Us

Laguna Hills, California/San Diego, Us

Minneapolis, Mn, Us

• Lead Corrective and Preventive Action (CAPA) projects to implement process improvements in the quality system and on the manufacturing line. Use root cause tools to perform investigation of quality issues. Determine appropriate action plan to address root causes and support implementation of actions. • Support daily manufacturing activities, including disposition of nonconforming product, equipment issues, and operator training.• Support New Product Introduction (NPI) projects for glucose sensor products. Lead quality efforts for transfer from design to manufacturing, including support for process validations, generation of risk assessment documentation, and generation of master validation plans and reports.

Minneapolis, Mn, Us

• Performed periodic tracking and trending of failure data for field returns of GI diagnostic catheters.• Performed root cause analysis and developed corrective actions addressing electronic failures in field returns using an A3 format. Led cross-functional team in flex circuit design troubleshooting, improvements, and characterization with FEA analysis.• Performed DOEs and process characterization for soldering processes.• Implemented manufacturing improvements to the returned product servicing area, including process standardization, WI development, and operator training.

St. Paul, Minnesota, Us

• Production support: Supported daily production issues in an ISO 7 class clean room such as equipment or tooling failures and component issues. Dispositioned non-conforming products, generated yield reports, and implemented process improvement projects. Maintained work instructions and trained operators on new or modified processes and inspections.• Validation: Managed revalidation efforts for the Cardiac Re-synchronization Therapy (CRT) leads product line. Performed process validation activities including range finding, IQ/OQ/PQ, test and inspection method validations, and writing improved manufacturing instructions and PFMEAs. • Quality issues: Identified and documented Non-conforming Material Reports (NCMRs). Performed engineering testing as needed to evaluate non-conforming product. Participated in root cause analysis and implemented correction activities to prevent future occurrences.• Leadership: Managed two direct-report co-op students; mentored co-ops on various tooling design, process validation, and equipment qualification projects. Led metrics reporting and trending for manufacturing data.

Attleboro, Ma, Us

• Equipment qualification: Performed debug and qualification of high volume, automated production equipment that manufacture automotive sensor products. Qualified vision inspection, assembly, calibration, electrical testing, and laser coding equipment for capacity expansions in Changzhou, China facility. Documented results (Gage R&R, Cpk) and trained global process teams.• New product development: Designed process flows for new safety critical sensors, performed process and design optimization testing, evaluated new equipment designs, supported prototype builds, and wrote PFMEAs. Interfaced with cross-functional team of design, quality, and mechanization engineers from conceptual design to production launch.

Bs, Mechanical And Aerospace Engineering

Education record