Role at a glance
- Job function
-
Software Engineering & IT Enterprise Applications & ERP
- Salary
- Not Disclosed
- Location
- Boudry, CH
- Work arrangement
- On-site
- Employment
- Full-time
- Experience
- 5+ years' Life Sciences industry experience and at least 2 years’ experience in MES
- Education
- Bachelor of Science in Engineering, Computer Science, or related fields
Spotted an issue?
We’ll check it against the original posting.
Role Summary
The EMES Recipe Author is responsible for enterprise recipe management and support of the Enterprise Manufacturing Execution Systems solution used across the BMS digital manufacturing network for clinical and commercial medicine production. The role supports global Biologics recipe management from requirements through build, testing, reporting, customization, and manufacturing support.
What You'll Do
- Support the global recipe management strategy and maximize reuse of recipes and recipe segments across sites.
- Partner with Supply Chain, MS&T, Quality, and Manufacturing Operations to understand business requirements and lead recipe delivery.
- Develop functional specifications, author recipes, facilitate demos and dry runs, and conduct Recipe User Acceptance Testing.
- Install and promote recipes and master data, and perform recipe and specification reviews and approvals.
- Gather and manage requirements for batch reports supporting Review by Exception and Release by Exception strategies.
- Provide Tier 3 escalation support, support end-user feedback and usability improvements, assess risks and impacts to the EMES solution,...
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Bachelor of Science in Engineering, Computer Science, or a related field; 5+ years of Life Sciences industry experience; at least 2 years of MES experience; at least 2 years designing and building recipes in automation and execution systems in regulated manufacturing environments; strong knowledge of IT applied to manufacturing, regulatory requirements, software validation, and IT/automation project delivery.
Required
- Bachelor of Science in Engineering, Computer Science, or related fields
- 5+ years' Life Sciences industry experience
- At least 2 years’ experience in MES
- At least 2 years’ direct experience designing and building recipes in automation and execution systems in regulated manufacturing...
- Strong domain expertise in the application of IT to manufacturing
- Strong knowledge of regulatory landscape and demonstrated experience with software validation
- Proven track record of successful IT/automation project delivery
Preferred
- Emerson Syncade experience
Original job description
Content provided by the employer
Original job description
Content provided by the employer
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
Responsible for enterprise recipe management and support of the Enterprise Manufacturing Execution Systems (EMES) solution that is utilized across the BMS digital manufacturing network to produce clinical and commercial medicine.
The EMES Recipe Author’s scope is supporting the global recipe management strategy including managing the Biologics network-based recipes from requirements to build testing and support, reports, and any customizations that support Biologics manufacturing and batch disposition operations.
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.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.
About the company
Bristol Myers Squibb
Large Enterprise
Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a focus on oncology, immunology, and cardiovascular health, the company leverages advanced science and technology to create transformative therapies that address critical unmet medical needs. Operating in more than 70 countries, Bristol Myers Squibb emphasizes collaborative efforts and strong partnerships in research and development to drive advancements in healthcare and improve patient outcomes worldwide.