Process Engineer

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 6000 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 Medicals website or on the role:The 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 Model: RemoteTravel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica Tijuana BC and Vega Baja PR youll 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 4000 hour or 2-year process engineering from a school in advanced molding or RJG Master Molder 2 (or equivalent).Certification in Basic Mold Flow (or equivalent) is a in Master Molding 3 is a of Experience:10 years of experience in processing and in a molding environment process development qualification validation of molds Knowledge :Extensive knowledge and able to train in: processing and process development techniques in scientific molding principles (MM2 skill level)PlasticsInjection 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 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 Requirements:Authorized to work in the proficiencyAbility to travel up to 75% to Viant sites (U.S. Costa Rica Tijuana and Vega Baja PR)