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MBR Verification Lead

Location: Zurich
Sector: Consulting
Job Type: contract
Salary: Competitive
Reference: BBBH583725

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: Zürich - limited home office

Start date: 01.01.2024

End date: 31.03.2024

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 cross-functional 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 +41 44 229 99 43 or Kaixi.jiawu(at)

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Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland.

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