Design-Win Distribution
Complex technical sales and manufacturing engagements across the global electronics supply chain.
Inside this journey
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Customer Discovery
Capture the project timeline, BOM deadline, allocation risks, target performance/power/size/cost constraints, and key stakeholders across engineering and procurement.
Discovery Questions
Tell Me About the Project That Just Kicked Off
- What is the project name or internal code so we can reference it consistently?
- What type of product are you building?
- Where are you in the development cycle right now?
- When is your BOM freeze or component selection deadline?
- How urgent does solving the component question feel to your team right now?
- Who on your team will be the primary owner for design decisions (name, role, and best contact)?
Is This Project Quietly Rushing Toward a Brick Wall?
- If your current prototype part becomes unavailable, what is the real downside beyond lead‑time—schedule slips, lost customers, or redesign cost?
- How would you rate the availability risk for your prototyped part right now?
- Have you identified second‑source candidates or cross‑vendor alternatives yet? If yes, which ones and why were they not chosen initially?
- How long have allocation or supplier availability issues been impacting your projects?
- How does the allocation risk make you feel about hitting the launch date?
- If allocation forces a redesign, what is the latest milestone you can tolerate that change without missing your delivery date?
Where the Performance Trade‑offs Actually Live
- Which of these trade‑offs are you secretly willing to sacrifice—power, performance, size, or cost—to keep the schedule?
- What is your target power budget for typical operation (mA or watts and conditions)?
- What minimum processing capability or benchmark must the MCU or module meet (e.g., MIPS, MHz, core architecture, DSP features)?
- Are there strict package or mechanical constraints that rule out common parts (max package size, pin count, lead frame vs. QFN vs. BGA)?
- What is the target BOM cost for the controller, PMIC, or module (per unit) that keeps your economics intact?
- Are there specific certifications or regulatory needs that influence part selection (e.g., functional safety, medical, automotive AEC‑Q, wireless approvals)?
Who's Responsible When Things Break at 9 PM?
- Who on your team will be on‑call for late‑night prototype debugging and who escalates supplier issues?
- Which roles must be involved from our side to make this collaboration successful (firmware, hardware, procurement, QA)?
- Who in procurement will own sample requests, cost negotiations, and lead‑time confirmations?
- When do you usually bring procurement into the conversation for a new design?
- What communication cadence and channels work best for your stakeholders during design‑in (e.g., weekly calls, shared board, Slack, milestone emails)?
What Have You Tried, and What Still Feels Broken?
- Which evaluation kits, reference designs, or vendor app notes have you already tested for this use case?
- When you used those evals, what were the top three technical issues that stopped progress?
- How long have those issues been blocking your team from moving forward?
- When you reached out to vendor support for those problems, how would you rate responsiveness and effectiveness?
- What would you most want a field application engineer to solve for you in week one of engagement?
- Would you prefer we first adapt an existing reference design to your board, or ship a new reference board for direct testing?
Imagine a Version of This Device That Actually Ships
- When you say 'production ready,' what invisible engineering or supplier checks do you assume are already done?
- Which acceptance tests must pass before procurement will place volume orders?
- What initial yield or failure rate would you accept during ramp to production?
- Do you require design registration or a manufacturer qualification step before committing to supplier pricing or allocation?
- What lead time and allocation guarantees would make you comfortable to lock into a supplier for production?
How Do Decisions Actually Get Made Here?
- If stakeholders argued over component choice, who has final approval and why?
- What decision criteria do you weigh when selecting a part—list the top criteria and approximate importance (e.g., cost 40%, power 30%)?
- Does your organization use formal vendor scoring, lifecycle cost models, or risk matrices in supplier selection?
- Are there contractual terms that would prevent you from choosing certain distributors or lines (exclusivity, price‑lock, long minimums)?
- What is the simplest internal win that would get this design past procurement and into a purchase order?
If We Partnered Right Now, How Would You Measure Our Help?
- If we could prove meaningful value in one week, what concrete result would you want to see?
- Which sample deliveries would accelerate your decision most: eval kit, production‑like sample, reference board, or working firmware?
- What timeframe do you need samples and initial test results to stay on schedule?
- How will you measure whether an FAE engagement was successful (select the top outcomes)?
- What would make you confident enough to register the design now rather than delaying registration until after production ramp?
- Would you like us to propose a next‑step plan with owners, dates, and required sample/eval deliveries?
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Solution Experience
Run FAE-led technical sessions using the customer’s prototype and scenarios to validate candidate parts, reference designs, and evaluation kit fit against required outcomes.
Technical Sessions
- Solution Experience Pre-Work & Alignment
- Prototype Intake & Baseline Validation
- Candidate Parts Validation Workshop (Hands‑on)
- Schematic Review & Reference Design Adaptation
- Validation Sign‑Off & Next Steps (Mutual Commit Prep)
Issues & Enhancements
- Customer engineering to review and mark any mechanical/firmware constraints within 3 business days.
- Produce side-by-side, measurable evidence showing which candidate(s) meet acceptance criteria.
- Identify necessary reference design changes and confirm eval kit fit or showstoppers.
- Elicit a clear validation signal (go/hold/fallback) from the customer for each candidate.
- FAE to export and share standardized test result packets (measurements, logs, photos) for each candidate.
- Customer to vote and record go/hold/fallback decision per candidate with rationale.
- FAE to list required reference design edits and an estimated FAE support hour budget.
- If no candidate passes, FAE to propose next experiments or alternate parts to evaluate.
- Review Chosen Candidate(s) & Rationale
- Finalize schematic change set and reference design adaptation list required for integration.
- Agree FAE deliverables, timelines, and estimated support hours for adaptation work.
- Document allocation risks and an agreed mitigation path (fallback parts, sample orders).
- FAE to deliver annotated schematic diff and reference design files within agreed SLA.
- Introductions & Objectives
- FAE to open sample requests for chosen primary and fallback parts and confirm lead times and costs.
- Record escalation contacts and a timeline for allocation risk mitigation steps.
- Summary of Evidence vs Acceptance Criteria
- Achieve formal validation sign-off or documented rejection for candidate parts based on evidence.
- Create a prioritized list of unresolved issues with owners and SLA timelines.
- Agree next milestones and ready the engagement for Mutual Commit and Deployment stages.
- FAE to produce and deliver the final evidence pack (test reports, annotated schematics, decision log).
- Customer to confirm sign-off on chosen part or record formal rejection and alternative path.
- FAE/Distributor to provide purchasing summary (costs, lead times, sample availability) for procurement handoff.
- Schedule first deployment checkpoint meeting and assign milestone owners in the shared plan.
- Crystal-clear one-sentence current state documented and agreed by all stakeholders.
- Concrete consequence statements (time/cost/risk) tied to the current state.
- Measurable future-state and acceptance criteria defined and accepted.
- All pre-work, artifacts, and logistics confirmed so the hands-on session can proceed without delays.
- Customer to upload prototype BOM, latest firmware, test vectors, and photos to shared workspace before workshop.
- Customer to deliver 1-2 representative prototype units and order of test scenarios to run.
- FAE to provision candidate parts, evaluation kits, measurement scripts, and baseline test plan.
- Schedule workshop time blocks and confirm primary/backup participants from customer and FAE teams.
- Physical & BOM Inspection
- Establish an auditable baseline dataset (power, performance, thermal) for the prototype.
- List and prioritize observed failure modes and their operational impact.
- Confirm reproducible test methods that will be used during candidate validation.
- FAE to produce and share baseline test report with raw logs and annotated photos.
- Customer to confirm any intermittent behaviors and supply additional test vectors if available.
- FAE to finalize the candidate test matrix (parts A/B/C, eval kits, and reference design variants).
- Brief Recap: Current State, Consequence, Future State
- Schematic Walkthrough & Power Sequencing
- Confirm Test Matrix & Roles
- One‑sentence Current State
- Unresolved Issues & Risk Register
- Smoke & Functional Sanity Tests
- Purchasing Inputs: Lead-times & Sample Costs
- Consequence Quantification
- Live Test: Candidate Part A vs Baseline
- Baseline Performance & Power Measurements
- Reference Design Adaptation List
- Live Test: Candidate Part B vs Baseline
- Agree Next Milestones, Owners & Dates
- Record Failure Modes & Allocation Risks
- Define Future-State Outcomes & Acceptance Criteria
- FAE Support Scope & Deliverables
- Logistics, Required Artifacts & Pre‑work
- Reference Design / Eval Kit Fit Assessment
- Confirm Measurement Methods & Acceptance Criteria
- Allocation & Risk Mitigation Plan
- Escalation & Communication Plan
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Solution Scope
Define the design‑in scope: sample and eval kit deliveries, reference design adaptations, FAE support hours, acceptance tests, and design‑registration terms.
Scope Configuration
- Provision evaluation kit with preloaded firmware
- Deliver reference design schematic and PCB layout
- Perform schematic review and provide redlines
- On-site or remote prototype debugging session
- Power-sequencing debug with lab measurements
- Supply production-intent samples with traceable lots
- Component cross-reference and alternate BOM
- Port and integrate MCU BSP and drivers
- Deliver thermal and power profiling data
- Assemble small-run prototypes from reference PCB
- Provide evaluation firmware examples and application notes
- Run compliance pre-test setup and deliver test data
Scope Questions
Provision evaluation kit with preloaded firmware
- Do you want evaluation kits delivered with preloaded firmware or delivered blank?
- Which firmware components should be preloaded (select all that apply)?
- How many evaluation kits do you need initially?
- What is the required delivery timeline for the evaluation kits relative to your BOM deadline?
- Are there firmware licensing, NDA, or export-control constraints we should apply before loading firmware?
- Please describe any special configuration, test scripts, or acceptance checks you want preinstalled on the kits.
Deliver reference design schematic and PCB layout
- Do you require a full reference schematic and PCB layout or only schematic/package-level guidance?
- What target board constraints matter most (board size, stackup, layer count)?
- Which CAD format(s) must deliverables be provided in?
- Do you need component footprints and 3D models included?
- What timeline and review cadence do you expect for reference design delivery?
- Please note any manufacturing constraints or preferred design rules (DFM, impedance targets, keepouts).
Perform schematic review and provide redlines
- Will you provide a complete schematic or partial sheets for review?
- What level of fix recommendations do you expect (informational notes, required redlines, suggested rework)?
- What is your acceptable turnaround time for a full schematic review?
- Do you need annotated PDFs, native CAD redlines, or both as deliverables?
- Are there specific failure modes or high-risk blocks we should prioritize (power, reset, IO levels)?
- Who on your team will own the review comments and track closure (name/role)?
On-site or remote prototype debugging session
- Do you prefer an on-site visit or a remote debugging session?
- What is the primary objective of the debugging session?
- How long should the debugging engagement be (hours/days)?
- What remote access capabilities will you provide (video, remote desktop, JTAG/serial/logs)?
- Are there security, access, or NDA requirements for the debugging session?
- Please list expected hardware and test tools to be available during the session (scope the environment).
Power-sequencing debug with lab measurements
- Which rails or subsystems require power-sequence debugging?
- Do you need time-domain measurements, scope captures, and annotated plots delivered?
- What measurement accuracy or instrumentation constraints are required (e.g., oscilloscope bandwidth, current probe)?
- Is the debugging focused on nominal operation, cold-start, brownout, or hot-swap conditions?
- Do you require test scripts or automation to reproduce the issue and for future regression?
- Please specify acceptance criteria or pass/fail thresholds for power behavior (voltage rise times, inrush current limits, sequencing windows).
Supply production-intent samples with traceable lots
- Do you require production-intent (authentic) samples or engineering/dev samples?
- How many production-intent samples and which lot traceability details do you require?
- Do you require specific date codes, country of origin, or manufacturing site traceability?
- Are there storage or handling constraints (humidity control, temperature, packaging)?
- What lead-time and delivery terms are acceptable for production-intent samples?
- Do you need certificates of conformance, material declarations, or traceability paperwork included?
Component cross-reference and alternate BOM
- Are you open to multi-vendor alternates or constrained to preferred vendors only?
- What attributes must alternates match (package, pinout, electrical spec, cost)?
- Do you need lifecycle/obsolescence risk ratings for alternates?
- How many alternate BOM options do you want evaluated per critical component?
- Do alternates require validation testing or only a technical fit assessment?
- Please list any banned or ROHS/exempt materials, or vendor approvals required.
Port and integrate MCU BSP and drivers
- Which MCU family and toolchain must BSP and drivers target?
- Do you require RTOS integration or bare-metal examples?
- What deliverables are required (source code, compile instructions, binary images, CI integration)?
- Are there license or IP constraints for including BSP/drivers in your product?
- What timeline and handoff format do you expect for BSP integration?
- Please describe required testing or acceptance criteria for the BSP integration (peripherals validated, power modes, stress tests).
Deliver thermal and power profiling data
- Which operating modes and workloads should be profiled (idle, peak, typical use cases)?
- Do you require thermal imaging, temperature vs time plots, and/or steady-state thermal maps?
- What power rails and measurement accuracy are needed (mW resolution, supply ripple specs)?
- What environmental conditions should testing cover (ambient temperature range, airflow, enclosure)?
- What format do you want the profiling deliverables in (raw data, MATLAB/CSV, annotated report)?
- Please specify any pass/fail thresholds for thermal or power metrics.
Assemble small-run prototypes from reference PCB
- How many prototype units do you need assembled?
- Do you require purchasing/part sourcing or will you supply the BOM and parts?
- What assembly standards and inspection levels are required (IPC class, AOI, X-ray)?
- Do prototypes require functional test fixtures or burn-in procedures?
- What lead-time and delivery packaging do you expect for assembled prototypes?
- Please note special handling, conformal coating, or rework instructions needed.
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Mutual Commit
Agree commercial and operational terms including sample costs, lead‑time commitments, design registration implications, and escalation paths for allocation risk.
Agreement Modules
- Statement of Work (SOW)
- Sample & Evaluation Kit Order Agreement
- Lead-Time & Allocation Commitment
- Design Registration & Pricing Hold
- Commercial Terms & Payment Schedule
- Escalation & Allocation Risk Plan
- Acceptance Criteria & Test Sign-off
- FAE Support & Service Addendum
- Change Order & Scope Amendment Procedure
- Confidentiality & IP Use Agreement
- Shipping, Returns & Warranty Terms
- Termination, Renewal & Transfer Terms
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Deployment
Schedule and execute evaluation deliveries, schematic reviews, lab debugging sessions, and milestone check-ins with clear owners and timelines.
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Success
Confirm design‑in outcomes, capture lessons learned, and transition to purchasing with documented part choices, production readiness notes, and open issues.
Success Reviews
- Design‑In Outcomes Confirmation
- Lessons Learned & Design Retrospective
- Production Readiness & Purchasing Handoff
- Open Issues Triage & Risk Mitigation Workshop
Issues & Enhancements
- If allocation risk remains high, trigger the agreed escalation workflow to secure supply.
- Schedule updates to the reference design repository and evaluation kit BOMs based on agreed changes.
- Plan a short FAE training session covering the identified failure modes and remediation steps.
- Add a 'design‑in checklist' item to future kickoff templates to capture allocation risk earlier.
- Approved BOM & Alternates
- Deliver a clear handoff packet (BOM, test evidence, design registration forms) that procurement can action immediately.
- Align on lead times, initial PO schedule, and contingency ordering to mitigate allocation risk.
- Define ownership and SLAs for supply escalations during the production ramp.
- Publish the handoff packet to procurement and confirm receipt and next steps.
- Submit design registration paperwork to the manufacturer(s) and track approval status.
- Create an initial PO timeline and place any recommended safety stock or NRE orders.
- Record escalation contacts and circulate the escalation flowchart to stakeholders.
- Open Issues Backlog Review
- Reduce the open issues list to a prioritized set with owners, mitigation plans, and deadlines for closure.
- Agree contingency parts and place any urgent eval kit orders to validate mitigations.
- Define verification checkpoints that, when passed, will enable procurement to proceed with confidence.
- Update the issue tracker with priorities, owners, mitigation steps, and deadlines from the workshop.
- Order identified contingency evaluation kits and schedule the required lab sessions.
- Schedule the verification checkpoints and invite necessary stakeholders for pass/fail validation.
- One‑sentence Current State
- Achieve explicit engineering sign‑off that selected parts meet acceptance criteria or list binary remaining gaps.
- Produce a definitive list of approved production parts plus alternates and any remaining open issues with owners and deadlines.
- Agree the exact artifacts to hand to purchasing (BOM, test reports, design registration, lead‑time notes).
- Finalize and publish the production BOM with part numbers, alternates, packaging, and orderable quantities.
- Upload acceptance test evidence and sign‑off form to the project folder and notify procurement.
- Assign owners and deadlines for each open technical or sourcing issue not closed in the meeting.
- Create a short exceptions log capturing known limitations or marginal cases to accompany the handoff.
- Pre‑read & Objectives
- Produce a prioritized lessons learned document with owners and timelines for each improvement.
- Ensure knowledge transfer to FAEs, product managers, and procurement so future projects avoid the same issues.
- Identify any necessary updates to reference designs or evaluation kits that remove common blockers.
- Draft and publish the lessons learned report and distribute to internal and customer stakeholders.
- Lead‑time & Allocation Risk Assessment
- Impact & Likelihood Prioritization
- Consequence Summary
- Timeline & Decision Log Review
- Cost, Design Registration, and Commercial Terms
- Evidence Review — Results & Test Data
- Mitigation Options & Contingency Parts
- What Worked / What Didn’t (Tech & Process)
- Gap & Open Issues Review
- Qualification & Acceptance Test Schedule
- Owner Commitments & Deadlines
- Root Cause & Impact Analysis
- Validation & Forced Confirmation
- Verification Checkpoints
- Improvement Backlog & Ownership
- Forecast & Initial PO Plan
- Escalation Path & SLA
- Sign‑off & Next Steps to Purchasing
- Publish & Communication Plan