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Position Summary:
This role is responsible for supporting product lifecycle activities, including new product introduction, product transfer, and ongoing manufacturing operations. This role ensures product quality, yield, and compliance through engineering evaluation, troubleshooting, and continuous improvement initiatives. This role will collaborate cross-functionally to drive process enhancements, cost optimization, and operational excellence, enabling smooth transition from design to production and sustaining high-performance standards throughout the product lifecycle.
Position Responsibilities:
Common Responsibilities:
Support and drive product transfer into manufacturing.
Perform data trending and analysis.
Apply FMEA, DOE, and statistical analysis to optimize product quality and reduce costs.
Drive process improvements, cost reduction, and product sustaining activities.
Manage Engineering Change Request and Notifications (CRs and CNs), including updates to work instructions and test requirements.
Support documentation: engineering drawings, BOMs, test reports, assembly procedures, and validation plans.
Participate in continuous improvement initiatives and operational excellence programs.
Frequent cross-functional collaboration and occasional travel to other sites.
Discipline-Specific Responsibilities:
Mechanical Engineering
Design & Development
Independently implement component/assembly changes (material, finish, tolerances).
Perform tolerance stack-ups define CTQs for parts.
Draft/execute DOEs for yield/quality issues.
Manufacturing Support & NPI
Own segment of transfer activities: golden unit builds, test setup calibration, GR&R plans.
Qualify alternate suppliers/materials execute PPAP/FAI with quality/manufacturing.
Quality, Reliability & Data
Lead failure analysis on recurring defects implement interim containment.
Apply SPC monitor Cp/Cpk propose corrective/preventive actions.
Perform basic DOE and SPC analysis for yield improvement.
Apply root cause analysis with quantitative evidence.
Provides charts/tables in reports rather than anecdotal statements.
Challenges unsupported opinions with data queries.
Communicates findings with clear visuals (Pareto, trend charts).
Project & Process
Plan small workstreams align deliverables with core team schedules.
Author ECRs manage scrap analysis and material disposition.
Documentation & Compliance
Generate detailed drawings, BOM updates, test reports, assembly procedures, validation protocols.
Maintain PLM integrity traceability to requirements/design inputs.
Collaboration
Engage suppliers/CMs for DFM feedback support builds at CM sites.
Position Requirements:
Typically requires a Bachelor's degree and a minimum of 2 years of related experience.
Proficiency in CAD systems (SolidWorks/Creo) with understanding of GD&T and DFMA principles.
Working knowledge of FMEA, DOE, SPC and manufacturing processes.
Experience using PLM systems (e.g., Teamcenter) and exposure to ERP environments (e.g., SAP/Oracle).
Advanced competency in Excel and familiarity with statistical tools (e.g., Minitab/JMP).
Preferably experienced in life sciences, biotech, or medical device environments.
Strong analytical thinking and clear, concise technical documentation.
Demonstrated ability to collaborate effectively with suppliers and cross-functional engineering teams.
Demonstrated ability to analyze data and propose fact-based, root-cause-driven improvements.
Proven ability to manage tasks to completion within defined timelines while maintaining high documentation accuracy.
Demonstrated ability to build strong working relationships with manufacturing and service teams and respond effectively to technical escalations.
Job ID: 152506989