Core Capability

Process & Manufacturing

Precision assembly, dispensing, and control systems for critical applications

Overview

Process automation is where product quality is made: assembly forces, dispensing volumes, coding rules, and recipe control must be repeatable and traceable. Motionwell builds process stations and integrated lines with a focus on measurable parameters, stable recipes, and validation-ready documentation (project-dependent).

Core Process Capabilities

Process areaTypical scopeCommon controls and verification
Precision assemblyPress-fit, welding, fastening, fixture controlForce/displacement logging, torque control, interlocks
Dispensing and fillingVolumetric or gravimetric dosing, multi-head stationsLevel or weight verification, feedback loops, alarms
Labeling and markingUDI/batch/expiry workflows, serialization-ready patternsOCR/OCV verification, reject handling, audit-friendly logs
Control platformsPLC/HMI/SCADA, recipe and parameter managementVersioned recipes, role-based access patterns (project-dependent)

Project References (Examples)

Project referenceProcess focusDelivered implementation (high-level)
Project 0023 (Pharmacy Automation)Coding and verificationSerialization-style coding with vision verification, HMI reporting, and controlled reject logic
Sealing & Filling Machine (custom equipment)Dispensing and sealingMulti-station dispensing and seal verification in a clean design (project-dependent)

Engineering Notes (How We Keep Processes Stable)

TopicPractical approach
Recipe governanceDefine what can change, who can change it, and how changes are recorded
Verification strategyDecide which parameters are measured every cycle and which are sampled
Exception handlingClear rework rules and error states prevent silent “good-looking bad parts”
Validation scopeAlign evidence collection with your quality system early (project-dependent)

Frequently Asked Questions

QuestionAnswer
How do you specify dispensing accuracy?We define the dosing method (volumetric/gravimetric), verification method (weight/level/vision), and acceptable tolerance. The fixture and fluid characteristics often matter as much as the dispenser.
Can you support UDI and serialization workflows?Yes. The key is defining your coding rules, verification criteria, data retention needs, and how rejects are handled and reported.
How do you manage product changeovers?We design tooling and recipes for controlled changeovers, then add verification checks so the line confirms the correct product and parameters before running.

To discuss process automation, contact us at /contact/ with your process steps, quality criteria, and data/validation expectations.

See process automation in action: Medical Automation | Electronics Automation

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