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Manufacturing Execution System (MES) Engineer - Level 3 jobs in United States
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Scalence L.L.C. · 2 days ago

Manufacturing Execution System (MES) Engineer - Level 3

Scalence L.L.C. is seeking a MES Engineer - Level 3 to drive digital transformation in a GMP-regulated manufacturing environment. The role involves leading the development and implementation of Manufacturing Execution Systems (MES) to enhance quality and compliance.
Information Technology & Services

Responsibilities

Support the deployment, integration, and configuration of MES platforms
Act as the primary site owner/subject matter expert for MES usage and training
Design and optimize process flows and electronic work instructions
Develop and maintain dashboards, KPIs, and reports for analytics and data visualization
Build automations and data pipelines to extend MES functionality and integration
Evaluate current processes and identify waste and bottlenecks
Lead Digital Ops Excellence projects using Lean or Six Sigma methodologies
Standardize and document best practices; facilitate workshops and training
Define data architecture for manufacturing data collection and storage
Deploy statistical analyses and machine learning for process optimization
Communicate insights and trends to stakeholders, connecting analytics to business outcomes
Champion data quality, governance, and traceability across various systems
Implement and adhere to GMP practices and regulatory requirements
Leverage MES capabilities to enforce production processes and capture records
Identify risks and develop mitigation plans to avoid delays and expenditures
Engage frequently with stakeholders across various departments
Present technical information clearly to technical staff and management
Provide work direction and ensure alignment with key leaders

Qualification

MES validationGMP experienceFDA regulationsBasic scriptingMES integrationTechnical innovationLeadershipProblem-solving

Required

Bachelor of Science in Engineering or related field. Equivalent education/experience considered
5 years in a manufacturing environment; medical device or life sciences preferred
Experience with MES validation and implementation
Minimum 2 years under GMP in a regulated environment
Basic scripting or low-code development
Technical innovation, leadership, and problem-solving abilities
Knowledge of FDA regulations and validation practices
Experience integrating MES with ERP and other systems

Preferred

MES platform certifications are a plus
MES/MOM Certificate is preferred

Benefits

7% bonus

Company

Scalence L.L.C.

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In today’s dynamic and competitive market, success hinges on mastering three key areas: Data Intelligence, Business Resilience, and Digital Experience.

Funding

Current Stage
Late Stage
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