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Mbr Verification Lead
vor 4 Wochen
**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**: 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)experis.ch
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