Process Engineer

Viant Medical
  • San Antonio, TX
    8 days ago

    Job Description

    About the company:Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With nearly 6,000 employees across 24 locations worldwide, it delivers high-quality, life-enhancing products with the scale and expertise to bring devices to market efficiently. Learn more at Viant Medical's website or on LinkedIn.About the role:The Corporate Process Engineer is responsible for leading advanced process development across the full lifecycle of molding and manufacturing programs, applying expert scientific molding and cavity pressure control principles to deliver robust, optimized processes. This role provides hands-on technical leadership for tooling design, process validation (IQ, OQ, PQ), and DOE execution, while supporting NPI, sustaining engineering, and business development initiatives. The Principal Process Engineer serves as a key technical interface between Viant, customers, tool shops, and internal teams to ensure regulatory compliance and best-in-class production outcomes.

    Work Model: RemoteTravel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana, BC, and Vega Baja, PR sites.

    What you'll do:

    Lead the process development cycleEvaluate processes for robustness, accuracy, and optimizationInitiate improvement projectsQuality/Metrology support: Assist site QE on KPI/KPO impacting part quality and process controlPartner with GTS/Site Tooling Engineer on design requirementsPartner with Tool Engineer on design and development requirementsSupport business development by selling tooling solutions and resolving processing issuesSupport corrective actions, re-validations, and tool/process optimizationOversee process development through I.Q. and O.Q. runs; report requiredComplete other related projects and tasks assignedDemonstrate expert knowledge and performanceApply scientific molding (Decoupled 2 and Decoupled 3)Expert in cavity pressure monitoring and control (RJG)Join technical reviews with customers and mold shopsSupport DFM and tool design reviews with Tool EngineersSupport molding cell development and executionSupport EOAT design and fabricationManage mold shop deliverables and expectations (SIM reports)Confirm receiving-site requirements (press/shot size/tonnage/special sequence) and machine capability studiesDevelop processes, review Moldflow data for start-up and debugTravel to customer sites, tool shops, and Viant facilities as needed; trip report requiredPrepare, track, and communicate Process DOEs, report results and recommendationsManage multiple concurrent projects (minimum 20 active)

    Requirements:Education:

    Bachelor of Science Degree in Engineering or related plastics discipline or 4-year engineering degree or equivalent completion of a 4,000 hour or 2-year process engineering apprenticeship.Certification from a school in advanced molding or RJG Master Molder 2 (or equivalent).Certification in Basic Mold Flow (or equivalent) is a plus.Certification in Master Molding 3 is a plus.Fully Bilingual (English & Spanish)

    Years of Experience:

    10+ years of experience in processing and in a molding environment, process development, qualification, validation of molds, etc.

    Job Knowledge :

    Extensive knowledge and able to train in: processing and process development techniques in scientific molding principles (MM2 skill level)Plastics-Injection Molding; LSR (preferred)Excel, PowerPoint, Word, and general computer skills; SolidWorks (drawing); 3D printing/3D software (preferred)Some knowledge in FDA, QSR, and ISO 13485 medical device regulations and standards.Understanding of statistics, Cp & Cpk studies for process. I.Q., O.Q. and P.Q. requirementsStrong understanding of DOE methods and implementationExpert knowledge of cavity pressure technologies and advanced control principlesFamiliarity with the various engineering grade thermoplastic resins and Mold Flow analysis."

    Additional Requirements:

    Authorized to work in the U.S.Ability to travel up to 75% to Viant sites (U.S., Costa Rica, Tijuana, and Vega Baja, PR)

    Numbers & Facts

    LocationSan Antonio, TX

    Skills

    • 3D Graphics Softwareunmatched
    • 3D Printingunmatched
    • Analysis Skillsunmatched
    • Automationunmatched
    • Business Developmentunmatched
    • Computer Skillsunmatched
    • Corrective Actionunmatched
    • English Languageunmatched
    • Extrusionunmatched
    • FDA (Food and Drug Administration)unmatched
    • ISO (International Organization for Standardization)unmatched
    • LinkedInunmatched
    • Machine Toolunmatched
    • Maintain Complianceunmatched
    • Manufacturingunmatched
    • Manufacturing Assemblyunmatched
    • Medical Equipmentunmatched
    • Metrologyunmatched
    • Microsoft Excelunmatched
    • Microsoft PowerPointunmatched
    • Microsoft Wordunmatched
    • Mold Designunmatched
    • Molding Processesunmatched
    • Multilingualunmatched
    • Multitaskingunmatched
    • Performance Metricsunmatched
    • Plastic Injection Moldingunmatched
    • Process Developmentunmatched
    • Process Engineeringunmatched
    • Process Improvementunmatched
    • Process Validationunmatched
    • Product/Service Launchunmatched
    • Public/Media/Press/Analyst Relationsunmatched
    • Quality System Requirements (QSR)unmatched
    • Regulationsunmatched
    • Scientific Principlesunmatched
    • SolidWorksunmatched
    • Solution Salesunmatched
    • Spanish Languageunmatched
    • Startupunmatched
    • Statisticsunmatched
    • Technical Leadershipunmatched
    • Training/Teachingunmatched
    • United States Department of Energy (DOE)unmatched
    • Willing to Travelunmatched

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