MBR Verification Lead
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)experis.ch
Check out all open positions at Experis at www.experis.ch
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.
