Shiftconnector® | Standard Work
Shiftconnector® brings standardized processes directly into the workflow so teams can execute, verify, and improve in real time with audit‑ready tracking.

Standardized processes are in the workflow so teams can execute, verify, and improve in real time with audit‑ready tracking.
Every single operator, every shift, every team on site follows the same validated workflows. Consistency creates quality — and audit-readiness.
Built-in audit trails, electronic signatures, and version control meet FDA 21 CFR Part 11, EMA Annex 11, and GAMP® 5 requirements — out of the box.
Data from ERP, MES, LIMS, and other systems is integrated into one shared, real-time view. Your teams see the big picture, not just a snapshot
Digitize Gemba Walks, Statistical Process Control checks, and process confirmations. Capture observations with context — photos, timestamps, notes, and location data.
Run checklists directly on the shopfloor and on any mobile device. Configure and update checklists without IT support, no revalidation required for layout changes.
SAMI surfaces high-variance steps, recurring deviations, and execution patterns from your documented checklist data — enabling data-driven continuous improvement.
Every action is logged with user, timestamp, and context. Full traceability for inspections and internal audits.
Document observations during Gemba Walks, Satistical Process Control Checks or process confirmations with photos, notes, and automatic timestamps. Link findings directly to improvement workflows.
Operators run mobile checklists (6S, line clearance, e‑logs), link anomalies to CAPAs or maintenance, and handoff to QA/QC with a complete history, ensuring no duplicate entry.
Leaders can review results in real time, adjust or update standard work templates quickly, and have automated actions whenever a defined condition occurs.
From standardized tasks to production plans, schedules and resources are in the same system supervisors use to coach and escalate.
Deviations from standard processes surface instantly; high‑volume records become automatic KPIs (OEE waterfalls, loss trees) instead of laborious manual counts—fueling daily improvement.
When standard work is digital and guided, everything changes. Our customers measure this every day.
faster incident reporting
less downtimes per month
reduction in compliance-related costs
Is your team struggling to ensure consistent execution of standards across shifts and sites?
We'll show you how to digitize standard work, ensure compliance, and free up time for value- adding activities — all without adding complexity.
Standard Work is not an isolated tool, but an integral part of the Shiftconnector® Intelligent Operations Platform.
Together with pillars such as Visual Management, OEE & Performance Reporting, or Continuous Improvement, it creates a continuous flow of information — from individual tasks to strategic decisions.
360° connectivity seamlessly integrates ERP, MES, and process historians into a common operational context.
Shiftconnector® integrates into your existing IT landscape, making it even more intelligent and efficient.

Fragmented OT/IT systems—MES, LIMS, QMS, ERP/CMMS, and historians—force teams to reconcile data by hand, slowing decisions and weakening traceability.
Shiftconnector® Intelligent Operations Platform unifies these sources into one audit‑ready operational timeline, giving production, quality, maintenance, and engineering the right information, at the right time.
Critical production knowledge is documented, but buried in logs, reports, and systems? The problem: When issues arise, finding the right information takes too long.
SAMI makes your documented knowledge instantly accessible. The AI-powered assistant understands your production context and retrieves relevant information in seconds - from the root-causes of incidents to proven solutions.
Learn from other pharmaceutical teams for your production
Discover how Shiftconnector® Go brings checklists, rounds, and standard work directly to operators' mobile devices.
Explore case studies, whitepapers, and insights from pharmaceutical production to support your operational excellence journey.
Standard Work digitizes SOPs, checklists, and operator rounds into guided, step-by-step workflows — ensuring consistent execution including built-in audit trails.
Yes. Built-in audit trails, electronic signatures, and version control meet FDA 21 CFR Part 11, EMA Annex 11, and GAMP® 5 requirements out of the box.
Absolutely. The checklist builder lets process owners create and modify checklists via drag- and-drop — no coding required.
Digitize Gemba Walks and process confirmations with mobile capture. Document observations with photos, notes, and automatic timestamps. Scan equipment barcodes to link entries directly to the technical location and to improve workflows.
A focused pilot can go live in 8–10 weeks. For global rollouts, we have completed deployments across multiple sites in four months.
Every production has its own compliance challenges and process requirements.
In a personalized demo, we'll show you how Standard Work solves your specific requirements and what results you can expect.