Solutions

One Record, Seen From Each Seat

Quality work fails at the hand-offs between roles. The same connected record, presented to each person as the part of it they own, is what removes the hand-off cost.

By role

Quality Manager

You need to know which launches are on plan and which documents are waiting on somebody. Open activities and pending approvals are visible as work rather than reconstructed from a tracker.

Quality Engineer

You build the PFMEA and the control plan. Both start from the process operations that already exist, so you are editing your own data instead of retyping it, and revisions are handled by the document rather than the filename.

APQP Engineer

You run the launch. Phases, activities, owners and dates live in a project that owns its deliverables, so "complete" means a released document exists.

Manufacturing Engineer

You define how the part gets made. Enter the operation sequence once and quality planning builds on it rather than transcribing it.

Process Engineer

You care which operation produces which characteristic and which control catches a problem. That relationship is the structure of the record, not a note in a cell.

Supplier Quality Engineer

You deal with several customers who each want something different. Requirement profiles hold each customer’s rules, so a submission knows what it owes.

NPI Team

You hand work between functions. One connected launch record means the hand-off is a state change, not an email with an attachment.

Quality Director

You need a view across parts and customers without asking four people to compile it.

Industries

Wherever a customer wants the evidence, not just the part

The method came out of automotive and it travels well. What these industries share is a customer who audits.

Automotive

APQP, PPAP and AIAG-VDA FMEA are the working vocabulary, and customer-specific requirements are the daily reality.

Aerospace

Long document trails, controlled revisions and traceable characteristics, where evidence has to survive years of scrutiny.

Medical devices

Design and process risk analysis with revision history, and records that keep their approval context.

Electronics

High characteristic counts per assembly, and process control that has to keep up with volume.

Industrial manufacturing

Mixed product families sharing processes, where the same operation serves several parts.

Machinery

Low volume, high complexity, and submissions assembled part by part.

Precision manufacturing

Tolerance-driven inspection and capability monitoring on characteristics measured in microns.

Consumer products

Several customers, each with their own format expectations for the same underlying data.

To be clear about what this list is. Naming an industry describes the quality workflows the product supports. It is not a claim of certification, regulatory clearance or validation for that industry, and we hold no such approvals today.
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