Core Solution

Medical & Pharmaceutical Automation

Precision assembly, cleanroom equipment, and GMP/FDA compliant systems for medical device manufacturers

Medical & Pharmaceutical Automation Excellence

Motionwell delivers automation solutions for medical device and pharmaceutical manufacturers in Singapore and the region, with a focus on precision assembly, cleanroom-compatible equipment, and compliance-ready engineering. We design for stable production, validated documentation, and long-term maintainability on the factory floor.

Medical Assembly Line

Automation Scope Across the Medical Value Chain

AreaTypical scopeCommon building blocks
Material handlingFeeding, singulation, tray loading, inter-station transportVibratory bowl feeders, linear tracks, vision-guided robotics, AMR/AGV logistics
Process and assemblyPress-fit, ultrasonic welding, torque fastening, dispensingServo transfers, pneumatic tooling, precision dispensing valves, recipe control
Inspection and testingCosmetic inspection, OCR/OCV, functional testsIndustrial cameras, strobe lighting, leak/pressure rigs, traceability logging
Serialization and codingBatch/lot and track-and-trace workflowsTIJ/laser printing, vision verification, reject handling, HMI reporting
End-of-linePrimary/secondary packaging and warehouse handoffBlister packaging, cartoning, case packing, palletizing, ASRS integration

Project References From Motionwell Deliveries

Below are project references used as concrete examples for system scoping and design discussions.

Project referenceScope (high-level)Key technologiesWhy it matters
Project 0023 (Pharmacy Automation)Serialization and vision inspection line with reject handlingCoding + OCR/OCV verification, HMI, pneumatic rejectCompliance-driven traceability and repeatable inspection
Project 0010 (Medical Pick & Place)Automated pick-and-place and packaging transfer workflowsStarwheel indexing for vial handling, gang pick & place, vacuum EOAT, sensorsGentle handling and stable indexing for high-volume medical parts
Rotary indexing assembly programHigh-throughput assembly with integrated vision and sorting12-station rotary indexing, BD-standard vision checks, Epson SCARA sortingCompact footprint, repeatable assembly, and fast station-to-station transfer

Medical Rotary Assembly Machine

FeatureImplementation detailOutcome
High-throughput indexing12-station rotary indexing tableStable cycle-to-cycle repeatability
Vision inspection standardBD-standard vision inspection with OK/NG sorting logicConsistent quality criteria and sorting control
Fast robot sortingEpson SCARA robot for high-speed placementEfficient downstream handling and separation
Cleanroom-ready designMaterials and design choices aligned to ISO Class 7/8 environmentsEasier cleaning and controlled contamination risk

Technical Specifications

ParameterSpecification
Configuration12-station rotary indexing table
Vision systemBD-standard compliance, contour inspection
RobotEpson SCARA for sorting and placement
EnvironmentISO Class 7/8 cleanroom compatible
IntegrationVibratory feeding, servo transfer, pneumatic assembly

Compliance, Validation, and Documentation

Medical and pharma projects succeed when engineering, documentation, and validation expectations are aligned early. We support compliance-driven delivery in a practical way.

Requirement areaTypical scopeTypical deliverables
Quality systemsISO-aligned build and service practicesDesign records, change control, FAT/SAT evidence
Cleanroom compatibilityISO Class 7/8 design constraints (project-dependent)Material selection notes, cleaning instructions, layout considerations
ValidationIQ/OQ/PQ support (project-dependent)URS/FS/DS, IQ/OQ protocols, execution records
Electronic records21 CFR Part 11 style traceability patterns (when required)User roles, audit trail strategy, data retention approach
Functional safetyCE/UL/ISO 13849 approach (project-dependent)Risk assessment, safety circuit design, safety test checklist

Integration and Data Traceability

Integration layerTypical protocol optionsExample usage
Machine controlPROFINET, Ethernet/IPStation handshakes and recipe control
Data collectionOPC-UA, file export, API gatewaysProduction records, inspection images, batch reports
Enterprise systemsMES/ERP interfaces (project-specific)Batch/lot reconciliation and production reporting

Frequently Asked Questions

QuestionAnswer
What cleanroom class can your equipment operate in?Many medical programs target ISO Class 7/8 environments. The final design depends on your cleaning SOP, materials selection, and how utilities and airflow are managed around the equipment.
Do you provide validation documentation?Yes. We can support FAT/SAT evidence and provide IQ/OQ deliverables when the validation scope is defined, including URS/FS/DS and protocol templates aligned to your quality system.
Can you integrate with existing MES/ERP systems?Yes. We typically define the traceability model first (IDs, timestamps, state transitions), then implement a stable interface using OPC-UA, industrial Ethernet, or an agreed file/API exchange method.
What is your typical project timeline?Medical automation timelines vary by validation depth and tooling complexity. A common range is 4–8 months from design kickoff through commissioning, with additional time for full validation where required.
Can you support UDI, coding, and serialization workflows?Yes. We have project references that include coding, OCR/OCV verification, reject handling, and operator HMIs. The critical factor is defining your compliance rule set and data retention requirements up front.

To discuss a medical or pharmaceutical automation project in Singapore, contact us at /contact/ with your product flow, target cleanroom class, and validation expectations.

Related capabilities: Material Handling | Process & Manufacturing | Inspection & Testing | Compliance & Standards

Ready to Automate Your Medical Production?

Contact us for consultation on medical device assembly, cleanroom automation, and GMP-compliant manufacturing solutions.

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