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Preston Brook, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly skilled MES PAS-X Specialist to join our team at Teva Pharmaceuticals. As a key member of our operations team, you will be responsible for providing system excellence for the MBR and MES within our manufacturing processes.Key ResponsibilitiesUpdate MBRs in the MES system for existing and new products based on approved...
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Preston Brook, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly skilled MES PAS-X Specialist to join our team at Teva Pharmaceuticals. As a key member of our operations team, you will be responsible for providing system excellence for the MBR and MES within our manufacturing processes.Key ResponsibilitiesUpdate MBRs in the MES system for existing and new products based on approved...
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Preston Brook, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly skilled MES PAS-X Specialist to join our team at Teva Pharmaceuticals. As a key member of our operations team, you will be responsible for providing system excellence for the MBR and MES within our manufacturing processes.Key ResponsibilitiesUpdate MBRs in the MES system for existing and new products based on approved...
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MES Designer
2 months ago
About Teva Pharmaceuticals
Teva is a global pharmaceutical company dedicated to improving access to high-quality healthcare for patients worldwide. We develop, manufacture, and market innovative and affordable medicines, specializing in sterile liquid products primarily used for treating respiratory conditions through advanced Blow-Fill-Seal technology and injectable Combination Products.
The Role: MES Designer
We are seeking a skilled MES Designer to join our team at our Runcorn facility. In this role, you will play a crucial part in ensuring operational excellence within our Manufacturing Batch Records (MBR) and Manufacturing Execution System (MES). Your responsibilities will encompass all aspects of PFS (Pre-filled Syringes) and BFS (Blow Filled Seal) operations, including updating and designing new configurations within the MES system to align with established Standard Operating Procedures (SOPs) for the governance and manufacture of our medicines.
Key Responsibilities:
- Maintain and update MBRs within the MES system for both existing and new products, ensuring accuracy based on approved production documentation.
- Enhance MBR functionality within the MES system to meet evolving site requirements.
- Evaluate product change controls and assess their potential impact on the MES and MBR systems.
- Conduct validation activities for upgrades and updates to SOPs and Work Instructions (WIs).
- Develop and update SOPs and WIs related to the MES system.
- Provide comprehensive training to new and existing staff members on MES functionalities.
- Actively contribute to a positive safety culture by identifying potential hazards and promoting safe work practices.
- Support root cause analysis efforts for fault identification and resolution.
Qualifications:
- A degree in a relevant field (engineering, IT, or scientific) is preferred but not mandatory.
- Proven experience utilizing an ERP system, particularly SAP manufacturing processes.
- Practical knowledge of MES systems, operations, and design principles.
- Relevant experience within the pharmaceutical industry or another highly regulated sector, focusing on business processes.
- Understanding of the IT system lifecycle within a GxP environment and the IT system validation process.
Skills and Attributes:
- Excellent communication, motivation, and teamwork skills.
- Ability to consistently deliver high-performance standards.
