MES SCO Technical Lead

Job Title: MES SCO Technical Lead

Location: Andover, MA (Onsite)

Duration: 6-12+ months Contract

Description:

RESPONSIBILITIES

• Lead the technical execution of the MES transformation project, ensuring it is configured correctly and meets production operational requirements.
• Define and document technical configurations and integration requirements in collaboration with Manufacturing Operations, Production, and Supply Chain teams.
• Perform software configuration and system integration testing to ensure MES functionality and alignment with manufacturing workflows and business needs.
• Act as a technical MES expert, supporting platform configuration, customization, testing, and implementation.
• Collaborate with Manufacturing Operations to ensure MES capabilities meet shop floor requirements and production tracking needs.
• Support production, engineering, and quality teams in transitioning to the new digital manufacturing workflows and real-time data capture processes.
• Drive hands-on execution of system configuration, integration testing, validation, and production workflow mapping activities.
• Design and implement integrations between Critical Manufacturing MES and enterprise systems (ERP, QMS, PLM, etc).
• Configure shop floor data collection, equipment interfaces, and manufacturing process definitions within the Critical Manufacturing platform.
• Provide input into future MES governance structure and technical roadmap as the manufacturing technology function matures.

MINIMUM QUALIFICATIONS

• Bachelor s degree in Information Systems or related field.
• 8+ years of hands-on experience with Manufacturing Execution Systems, preferably with Critical Manufacturing platform.
• Strong understanding of manufacturing operations, production processes, and shop floor workflows in regulated industries (medical device, pharmaceutical preferred).
• Demonstrated experience with MES configuration, customization, and integration with enterprise systems (ERP, QMS, PLM).
• Experience with software testing, QA validation, and requirements documentation.
• Technical proficiency in system integration approaches including APIs, web services, and middleware platforms.
• Knowledge of FDA 21 CFR Part 11 and other regulatory requirements for electronic manufacturing records.
• Strong analytical and problem-solving skills with ability to translate manufacturing requirements into technical solutions.
• Excellent communication skills with ability to work effectively with both technical and operational stakeholders.
• Self-motivated with ability to work independently and manage multiple priorities in a fast-paced environment.

PREFERRED QUALIFICATIONS

• Direct experience implementing or supporting Critical Manufacturing MES platform.
• Experience in medical device or other highly regulated manufacturing environments.
• Knowledge of Industry 4.0 concepts, Industrial IoT, and smart manufacturing initiatives.
• Familiarity with data analytics and reporting tools for manufacturing intelligence.
• Experience with serialization, track and trace, and genealogy requirements.