Manufacturing Execution System (MES)

Requirements
  • GEO: USA and Canada
  • Company Size: 500+ Employees
  • Industries: Manufacturing, Medical Device, Pharmaceutical, Surgical and Medical Instruments and Apparatus except Diagnostic Substances and Medical Laboratories
  • Titles: Manufacturing, Engineering and Technical, Information Technology, Operations
  • Job Level: Manager +
Overview

The most common types of production systems used by life sciences manufacturers today are either paper based, digitized but disconnected, or legacy manufacturing execution systems (MES). Paper-based systems are no longer practical for modern manufacturers. Manufacturing organizations that rely on multiple point solutions to digitize production processes still contend with disconnected systems, standalone spreadsheets, and scanned documents. Meanwhile, the costs and complexities of traditional MES software make it unfeasible in most production environments. As manufacturing becomes more data-driven and flexible, these production systems are increasingly unsustainable.

In data-driven manufacturing environments, production systems empower organizations to unlock the power of their data and remove the inefficiencies of disconnected data. The future of manufacturing execution is a data-first approach to information, systems, people, and processes – where electronic batch records (EBRs) or electronic device history records (eDHRs), training documents, standard operating procedures (SOPs), and more are quickly and cost-effectively digitized under one platform. 

Top reasons our community cites for adopting or considering this solution:

  • Inefficient processes causing errors and rework.
  • Poor data quality because production data isn’t captured consistently or accurately.
  • Burdensome validation for software changes.
  • Unplanned downtime due to deviations.
  • Takes too long to see production issues because of lack of process data.
  • Product releases are delayed by burdensome quality checks or quality issues.

You must be directly involved in your company’s evaluation process for solutions like this, or in the management chain for people who do. You must be a hands-on user of the prospective solution or in the management chain of users. Please do not register for programs that are an unlikely fit. Your credibility and ours depend on it.

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