Dale Scott Tollefson Email & Phone Number

Rice Creek Campus

- Define, develop, evaluate and verify PCD designs and proposed changes.- Participate on corrective action teams to resolve product issues.- Interface w/ multiple functional disciplines for design input, requirements & solutions to problems.- Act as a liaison with external suppliers to ensure continuity of product supply.

8200 Coral Sea Street Ne - Mounds View Campus, Mn 55112

7000 Central Avenue Ne - Minneapolis, Mn 55432 Rice Creek Campus

- Create and complete change notices for sub-tier suppliers.- Collaborate with Product Issue Escalation for non-conformances released to the field.- Perform new product qualifications. - Act as a liaison with external suppliers to ensure continuity of product supply.

Minnetonka, Mn

- Initiate CRs & drive through to completion (using Windchill) for my seven CATD product value streams: (Engage, Ultimum, Fast-Cath, Maximum, Swartz Introducers, BRK Needles, and Introducer Accessories.) - Review & approved over 400 CR requests initiated by other groups, from my seven value stream products.- Collaborate with/ assist product team members: (Marketing, Mfg, Clinical, Suppliers, CAD, Reg. Affairs, etc.) - Other duties include, document & drawing redlining (using Acrobat), data mining, tolerance stack-ups etc.

Mounds View, Mn

- Generate ECR/ECO continuation solutions for an AFS/EPS RoHS compliance effort to the entire line of catheters and accessories (using Enovia) – also had some Agile training.- Created over 81 new RoHS compliant part numbers with BOMs for review and approval- Orchestrated the lead-free solder Corrosion Testing effort with Materials Eng, lab techs and mfg eng.

Little Canada, Mn

Completed DHF Remediation project: ACross Transseptal Access System - Completed DHF EnSite Array Catheter: authoring Assessments & locating docs - Functioned as an Internal Auditor for assessments, plans, reports and indexes- Completed Windchill owner/approver training – using as a tool for doc. research

Generated creative continuation solutions for legacy Lead components for CRDM’s Therapy Delivery Systems Division – Global Product Team. - Generated over 150 CFI ranking reports for legacy Leads & components- Completed spec gap analysis on 94 legacy lead components that needed to meet FDA requirements of consistency between drawing notes, IP procedures and workmanship standards before promoting to review and approval using: Enovia V6, SiteBuilder, BQMS, MRCS, EQDMS and QADocs- Involved in the approval of over 130 ECR/ECOs with TD Released Products- Participated in lead design issue problem solving discussions w/ team & suppliers- Supervised the on-boarding and mentoring of two new contractor engineers - Reviewed drawings, create electronic redlines and interface with CAD Engineers to drive home all updates & changes using Adobe Acrobat on Pro-E Wildfire dwgs- Provided Lab measurements and digital photos of components w/ the microscope- Created technical illustrations for clarity in internal plans, reports & other FDA related documents

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B.S.I.D., Product Development, 3.2

Activities and Societies: National Honor Society/ Industrial Designers Society of AmericaGraduated with honors, Cum Lauda

Non-Declared, Biblical & General Studies, 3.2

Activities and Societies: Band (trumpet)

Diploma, Pre-Engineering

Activities and Societies: National Honor Society, Bible Study, Band, Audio VisualPre-Engineering (all Maths, Sciences and Industrial Ed.

Elementary School Completion, General Studies