What are the responsibilities and job description for the MES (Manufacturing Execution System) Architect position at Macrosoft?
Role : MES Architect
Duration : 12 Months (high chances of extension)
Location : Somerset, NJ
Mode of Work : 4 days onsite
Job Summary :
We are seeking an experienced MES (Manufacturing Execution System) Architect with expertise in Tulip to design, implement, and manage our MES solutions within a biotech environment. This role will be responsible for leading the architecture and deployment of Tulip’s platform across manufacturing operations, ensuring seamless integration with existing systems while meeting the specific regulatory and operational needs of a biotech company.
The MES Architect will work closely with cross-functional teams such as production, quality, IT, and compliance to ensure that the digital manufacturing strategy aligns with business goals and regulatory requirements.
Key Responsibilities :
- Architecture & Design :
- Lead the architectural design and roadmap of the Tulip MES platform in alignment with the company's manufacturing digital transformation strategy.
- Define system requirements and develop scalable solutions that meet the specific needs of the biotech manufacturing environment, including GMP compliance.
- Establish data models, workflows, and user interfaces that support efficient and compliant manufacturing processes.
- Implementation & Integration :
- Oversee the deployment of Tulip’s MES solutions across multiple production sites, ensuring smooth integration with existing ERP, LIMS, and other enterprise systems.
- Collaborate with production teams to design workflows, digital work instructions, and dashboards tailored to the manufacturing process.
- Ensure data flow integrity between MES and critical systems (e.g., PLC, SCADA, historians).
- Customization & Optimization :
- Customize the Tulip platform to meet specific production and operational needs, incorporating features such as digital twins, IoT integrations, and real-time data analytics.
- Continuously optimize the platform’s performance, user experience, and scalability.
- Regulatory Compliance :
- Ensure that the MES platform adheres to biotech / pharma regulatory standards, including FDA 21 CFR Part 11 and GMP requirements.
- Develop and implement validation protocols, change control processes, and ensure audit-readiness of the system.
- Collaboration & Communication :
- Act as a liaison between IT, production, and quality teams to gather requirements and provide MES-related solutions.
- Provide guidance and mentorship to junior team members and system users, developing training materials and conducting workshops.
- Innovation & Strategy :
- Stay current with emerging MES technologies and industry trends to introduce innovative solutions.
- Provide strategic input to management regarding MES investments, upgrades, and lifecycle management.
