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Senior Quality Engineer

TriMas Corporation

Clinton Township, MIFull-timePosted 6mo agoSeen in employer's feed 6 days ago

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At a glance

Compensation
No compensation found
Location
Clinton Township, MI
Schedule
Full-time
Work Authorization
Not specified

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Job overview

TriMas Corporation is hiring a Senior Quality Engineer. Omega Plastics, Inc. is seeking a Senior Quality Engineer to spearhead non-conformance, CAPA, and customer complaint activities. This role involves developing and reviewing validation protocols, supporting Quality Management System development, and leading software validation projects. The engineer will also review and approve documentation and support New Product Introduction processes.

Key focus areas include Spearhead Non-Conformances, CAPA, SCAR, and customer complaints activities, Develop, and review IQ/OQ/PQ Validation Protocols, Summary Reports, Validation Master Plans, and Support Quality Management System development by creating Procedures and Work Instructions.

Important skills include Non-Conformances, CAPA, SCAR, Customer Complaints Activities, Root Cause Investigations, and Material Disposition.

Skills & qualifications

RequiredNice to have

Skills

Non-ConformancesCAPASCARCustomer Complaints ActivitiesRoot Cause InvestigationsMaterial DispositionRisk AnalysisCorrective Action Preventative Action Plan ImplementationIQ/OQ/PQ Validation ProtocolsSummary ReportsValidation Master PlansISO 1348521 CFR 820 RegulationsQuality Management System DevelopmentProcedures and Work Instructions CreationSoftware Validation ProjectsDocumentation CreationTest PlansUser Requirement Specification (URS)Test Method Validation (TMV)Risk Management DocumentationProcess Flow Diagram (PFD)pFMEAControl Plan (CP)ISO14971Quality PlansInspection ReportsChange ControlsNew Product Introduction (NPI)Process Development ProcessesInternal AuditCollaborate With Teams

Full job description

Omega Plastics, Inc. has an opening for a Senior Quality Engineer at 24401 Capital Blvd., Clinton Twp., MI 48036. 40 hrs/wk. 9am - 5pm. M-F.

Responsibilities:

Spearhead Non-Conformances, CAPA, SCAR, and customer complaints activities which include root cause investigations, material disposition, risk analysis, and implementation of Corrective Action Preventative Action Plan.

Develop, and review IQ/OQ/PQ Validation Protocols, Summary Reports, Validation Master Plans for products, and manufacturing processes per ISO 13485, and 21 CFR 820 regulations.

Support Quality Management System development by creating Procedures and Work Instructions in support of ISO13485 and 21CFR820 compliance.

Lead Software validation projects to include documentation creation – Test Plans, User Requirement Specification (URS), protocols, Test Method Validation (TMV), and Summary Reports; generate Risk Management Documentation – Process Flow Diagram (PFD), pFMEA, and Control Plan (CP) per ISO14971 for process, product, and secondary operations.

Review and approve documentation such as Quality Plans, Inspection Reports, Change Controls, and Non-conformances to release for validation and commercial activities.

Support New Product Introduction (NPI) and Process Development processes which include feasibility, kickoff, and gate reviews.

Conduct Internal audit, collaborate with teams to resolve findings, generate needed records and reports.

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