MES Analyst

Baylis Medical Technologies is a leader in the development and manufacturing of innovative medical devices. The MES Analyst is responsible for the technical implementation of MES software, collaborating with cross-functional teams to analyze operational needs and ensure effective system utilization while supporting digital manufacturing initiatives.

Responsibilities

• Design, configure, and maintain MES applications to support manufacturing operations
• Collaborate cross-functionally to translate business needs into MES solutions
• Plan and oversee the deployment and layout of MES related workstations in manufacturing areas
• Interface with cross-functional teams and manufacturing personnel to ensure smooth implementation of changes
• Support the integration of MES with ERP, and other manufacturing systems
• Troubleshoot MES-related issues, perform root cause analysis, and coordinate resolution with IT, and Operations, ensuring minimal disruption to manufacturing processes
• Develop and maintain MES-related QMS documentation including, work instructions, and training materials, protocols and reports, and other documents such as trace matrices, test cases, and validation protocols and reports
• Provide user support, training, and documentation to enable effective system utilization
• Support system enhancements, upgrades, and continuous optimization of MES functionality
• Ensure compliance with GMP, FDA, and other regulatory standards in system configuration and validation
• Support business leaders on Long-Term MES strategy for the business
• Maintain MES master data, workflows, routings, and process parameters to ensure accuracy and consistency
• Collect, analyze, and interpret manufacturing data from MES, equipment, and other operational systems
• Develop dashboards, reports, and KPIs to monitor process performance, yield, cycle time, throughput, and compliance
• Identify trends, gaps, and process risks using statistical and analytical methods
• Support data-driven decision-making by providing actionable insights to engineering and operations leadership
• Ensure data integrity, traceability, and alignment with quality and regulatory requirements
• Identify opportunities to reduce variation, waste, and manual effort through process, system, or automation improvements

Skills

• Bachelor's degree in Industrial, Mechanical, or Biomedical Engineering, or a related technical discipline
• 1-4 years in a manufacturing environment
• Familiarity with ISO13485, 21 CFR Part 820, FDA inspection readiness
• Advanced skills in MS Excel
• Strong logical thinking and ability to interpret data trends
• Exceptional ability to communicate technical concepts to non-technical stakeholders across different departments
• Strong analytical and problem-solving skills
• Systems thinking and attention to detail
• Ability to translate data into actionable insights
• Effective cross-functional communication
• Self-driven with a continuous improvement mindset
• Ability to manage multiple priorities in a fast-paced environment and work under strict compliance standards
• Experience working in a medical device industry or highly regulated industry
• Experience with system integration (ERP, MES etc.)
• SQL knowledge

Benefits

• Complimentary shuttles and subsidized transit options
• Hybrid model and flexible hours
• One dedicated day off for impactful volunteering
• Abundant opportunities for on-site training, workshops, and personal development
• Tuition reimbursement
• Health spending account
• Employee-led clubs, campaigns, sports teams, and exhilarating activities

Company Overview