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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Senior Specialist - MES Platform Engineer

Enterprise ApplicationsConfirmed live in the last 24 hours
Full-timeLeiden, NetherlandsNo salary listedIn-person

About the Job

Requirements

  • Strong understanding of Manufacturing Execution Systems and manufacturing processes.
  • Experience with MES recipe authoring, configuration management, and system administration.
  • Knowledge of Good Manufacturing Practice, GxP, Data Integrity, and Computer System Validation practices.
  • Experience managing master data, user access, and system configuration.
  • Proficiency in troubleshooting, root cause analysis, system monitoring, and performance optimization.
  • Experience supporting MES upgrades, change management, and validation activities.
  • Ability to work effectively in a highly regulated biopharmaceutical manufacturing environment.
  • Experience with Emerson Syncade MES, SQL, ISA-95, MES reporting, label and form design, change control and validation processes, incident and problem management, and data integrity principles.

Responsibilities

  • Manage and maintain the MES application environment, including integrations and peripheral devices such as scanners and label printers.
  • Monitor MES application health, availability, performance, and underlying hardware components.
  • Support installation, configuration, upgrades, patches, and lifecycle management activities.
  • Perform routine system reviews and execute corrective and preventive measures to maintain system reliability.
  • Collaborate with Shared Services and infrastructure teams to define and manage application versus infrastructure responsibilities.
  • Design, configure, document, and maintain Master Recipes using standardized corporate objects and approved building blocks.
  • Analyse business requirements and translate operational processes into MES solutions.
  • Maintain and enhance existing recipes while ensuring consistency, usability, and compliance.
  • Evaluate and implement new objects, templates, and configuration components supporting recipe development and manufacturing improvements.
  • Execute master data management activities to ensure data integrity and consistency within MES.
  • Manage MES user access in compliance with approved procedures and regulatory requirements.
  • Support periodic access reviews and maintain appropriate segregation of duties.
  • Configure and maintain MES system settings supporting manufacturing operations.
  • Create and maintain MES reports, labels, label formats, and related configuration designs.
  • Support manufacturing operations through effective reporting and labelling solutions.
  • Maintain documentation and traceability related to MES configuration changes.
  • Develop and execute testing activities supporting new recipes, system changes, and MES enhancements.
  • Support creation of User Acceptance Test scripts and validation deliverables.
  • Participate in dry runs, qualification activities, and validation reviews.
  • Ensure MES solutions remain compliant with GMP, GxP, Data Integrity, and Computer System Validation requirements.
  • Support risk assessments, impact assessments, and change control activities.
  • Support MES upgrade projects, platform enhancements, and technology lifecycle initiatives.
  • Identify opportunities to optimize MES processes, improve user experience, and increase manufacturing efficiency.
  • Partner with local and global MES teams to implement best practices and standardized solutions.
  • Contribute to the long-term MES roadmap and system sustainability initiatives.
  • Provide second-line support for MES incidents, service requests, and operational issues.
  • Troubleshoot application, configuration, recipe, integration, and performance issues.
  • Restore MES availability in alignment with business continuity requirements, urgency, and severity classifications.
  • Participate in investigations and implementation of corrective actions related to MES events and deviations.
  • Work closely with Manufacturing, QA, MSAT, CSV, and IT stakeholders to ensure MES solutions meet business needs.
  • Collaborate with peer MES administrators and recipe authors across CTF sites.
  • Assist the Senior Manager Manufacturing IT Systems & MES in responsibilities associated with Technical System Ownership, Configuration Item Ownership, governance, and continuous improvement initiatives when required.

About the Company

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Bristol Myers Squibb discovers, develops and sells prescription medicines for serious illnesses, including cancer, blood disorders, immune diseases and heart disease, for patients treated by doctors and hospitals around the world. Its best-known drug is Opdivo, an immunotherapy that helps the body's own immune system find and attack many kinds of cancer. Researchers develop drug candidates in its labs or bring them in through acquisitions and partnerships, then test them in clinical trials to win regulatory approval. The company makes and markets the approved medicines and earns its revenue from sales of patent-protected drugs. Its roots go back to a business founded in 1887, and it is based in Lawrence Township, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Lawrence Township, NJ
Founded
1887

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