MBR/MES Designer

at  Teva Pharmaceuticals

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MBR/MES Designer
Date: Jul 25, 2024
Location:Runcorn, United Kingdom, WA7 3FA
Company: Teva Pharmaceuticals
Job Id: 57042

WHO WE ARE

We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. We are Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world. We’re currently recruiting for a MBR/MES Designer to join our team on a full time, permanent basis in Runcorn.
At Teva Runcorn, we develop, manufacture and market innovative and affordable medicines, specialising in sterile liquid products mainly used for treating respiratory conditions using Blow-Fill-Seal technology as well as injectable Combination Products.

WHO WE ARE LOOKING FOR

Do you have?

• Degree in relevant field is preferred but not essential (engineering, IT, Scientific)
• Experience of using an ERP system
• Current/previous user of SAP manufacturing processes
• Practical knowledge about MES, Operations and Design.
• Relevant Pharma experience or another highly regulated industry, in relation to business processes.
• Understanding IT system lifecycle in GxP environment and IT system validation process.

Are you?

• Good communicator / motivator / team player.
• Able to deliver high performance standards.

If so - we would value hearing from you!

TEVA’S EQUAL EMPLOYMENT OPPORTUNITY COMMITMENT

At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.
Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients. That is why we are constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice.
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• Update MBRs in MES system for existing and new products based on approved production documents.
• Update MBRs with functionality based on site requirements.
• Evaluate product change controls and impact on MES / MBR.
• Validation for upgrades and SOP/ WI updates
• Update / creates SOP / WI for MES.
• Support training of new and existing staff.
• Have an active involvement in promoting site safety culture raising safe and unsafe conditions or acts through the correct channels.
• Support route cause analysis for fault finding.