Manufacturing Execution System (MES) Recipe Author
About the role
Duties/Responsibilities
- Support global recipe management strategy to maximize reuse of recipes and/or recipe segments across sites.
- Build recipes that are designed around simplicity, flexibility, and cost effectiveness.
- Partner with MS&T and Process Robustness team to configure recipes in support of analytics.
- Lead recipe delivery process including.
- Partnering with Supply Chain, MS&T, Quality, and Manufacturing Operations to understand business requirements.
- Development of functional specifications.
- Recipe authoring, demos, and dry run facilitation.
- Recipe User Acceptance Testing.
- Recipe and master data installations and promotions
- Ensure recipes are built with consistency and adhere to guidelines.
- Perform recipe and specification review and approvals.
- Gather and manage requirements around batch reports that relate to the Review by Exception and Release by Exception strategies.
- Tier 3 escalation support of Pharma recipes and process to minimize disruption to manufacturing and/or impact to product.
- Support strategy for collecting end user feedback and improving the usability and user experience of the overall EMES solution.
- Support risk and impact assessment that changes, patches, outages, or other events can have to the EMES solution and the global network and define mitigation strategies. k. Support a knowledge management strategy including generating training content and mentoring.
- Promote compliance with data integrity and computer system validation requirements and regulations.
- Promote compliance by understanding change and the impact to the validated state of the application and underlying infrastructure.
Qualifications
- Bachelor of Science in Engineering, Computer Science, or related fields with 5+ years' Life Sciences industry experience and at least 2 years' experience in MES (preferably Emerson Syncade).
- At least 2 years' direct experience designing and building recipes in automation and execution systems (Syncade, PI Data historian, etc.) in regulated manufacturing environments.
- Strong domain expertise in the application of IT to manufacturing, including a broad understanding of processes and how they are supported by IT tools and systems.
- Strong knowledge of regulatory landscape and demonstrated experience with software validation.
- Proven track record of successful IT/automation project delivery
- Ability to work across global sites and cultures.
- Ability to travel up to 10% domestically and internationally.
We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.
How We Work
Where you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.
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