Mbr Verification Lead

vor 1 Woche


Basel, Basel-Stadt, Schweiz Experis Vollzeit

MBR Verification Lead
Experis is the global leader in professional resourcing and project-based workforce solutions.

Overview of contract


On behalf of our client, a large Consultancy company in Switzerland, we are looking for a MBR Verification Lead for the pharma industry.


Location:
Basel - home office possible

Start date:

End date:

Main responsibilities

  • Gather requirements for the creation of Manufacturing Batch Records (MBR), Good Manufacturing Batch Records (GMBR), and Equipment Specification Documents (ESP).
  • Conduct thorough testing and review of created MBRs to ensure accuracy and compliance with regulatory standards (GxP, GAMP, 21 CFR).
  • Actively participate in clarification sessions to refine and optimize the documentation process.
  • Utilize experience with SAP-MES interface, L2 integrations, and LIMS integration to enhance manufacturing documentation systems.
  • Collaborate with crossfunctional teams to ensure seamless integration of documentation systems.
  • Contribute to maintaining the highest standards in pharmaceutical manufacturing documentation.
  • Play a pivotal role in the pursuit of operational excellence within the pharmaceutical manufacturing domain.

Your skills:

  • Demonstrate a keen attention to detail and strong analytical skills in navigating complex manufacturing environments.
  • Experience on SAP-MES interface,L2 integrations, LIMS integration
  • Excellent communication skills in English, German is a plus
If you are interested in this opportunity, we look forward to receiving your CV or if you have any questions, contact Kaixi Jia on or

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