MES & Serialization Analyst - Freelance Contract - The Netherlands

Panda International
Geplaatst op
2 tot 6 maanden
Op locatie
MES & Serializiation


For one of our pharmaceutical clients in the Netherlands, we are currently looking for a freelance MES & Serialization Analyst.

In this role you are responsible to support the development and deployment of Manufacturing Execution System (Werum PAS|X) and Serialization related system components as part of our clients' Serialization projects. This position will provide daily project support for these systems in order to implement Serialization capabilities on their packaging lines.
This position will interact with the MES System Owner, MES and Serialization IS CoE (Centers of Excellence) in our clients' global network to assist with the development and the deployment of new functionality.

In this role, the Analyst will be responsible for performing the analysis and design associated with new requirements. The analyst will work closely with the IS Infrastructure teams and with the Computer Systems Validation group to ensure that all systems are implemented in a quality manner and in compliance with regulations.

Your role

  • System development and day-to-day project support

  • Point of contact for system design and troubleshooting

  • Maintain compliance with 21 CFR Part 11 for computerized systems

  • Ensure system administration operating procedures are accurate, effective and being followed

  • Create and maintain design and configuration specifications

  • Perform testing and develop documentation in support of system changes

  • Learn and support additional Information Systems where required

Your profile

  • Degree in Computer Science, Information Systems, Engineering, or Life Sciences

  • 4+ years’ experience in application development, system administration, or application support

  • Experience with Manufacturing Execution Systems and interfaces e.g.

  • OLE for Process Control (OPC) is essential

  • Experience with enterprise systems, validation, testing and change control

  • Experience using a document management system for authoring, reviewing and approving systems documentation

  • Strong team player who is able to collaborate with colleagues on complex tasks in a global environment

  • Pharmaceutical or biotechnology experience

  • Experience in supporting systems in a GMP regulated environment

Are you the candidate we are looking for?

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