MES MasterControl Administrator - Manufacturing Systems

Cirtec Services GmbH; Lowell (MA); On-site; USD 70,000 - 85,000; Full time

Benefits offered by this job

Training and career development

Healthcare and well-being programs

Paid Time Off and 401(k) with company

Job summary

Cirtec Medical Corporation seeks a Manufacturing Systems Administrator to manage MasterControl Mx, MES, and eDHR in a regulated manufacturing environment. You will ensure data integrity, regulatory compliance, and continuous improvement while partnering with Engineering, Quality, and Production teams.

The role emphasizes system validation, updates, and training material creation, with on-site responsibilities and a focus on cGMP and ISO standards.

Qualifications

• Bachelor's or master's degree in Systems Engineering, Computer Engineering, Industrial Engineering, or a related engineering field.
• Experience in systems administration within a regulated manufacturing environment, such as medical devices, pharmaceuticals, or biotechnology.
• Strong knowledge of MasterControl, specifically the Manufacturing Excellence (Mx) Suite.
• Experience with MES/eDHR systems and API-based system integrations.
• Experience working with integrated enterprise systems such as ERP, EDMS, or QMS.
• GxP/GMP experience strongly preferred.
• Strong technical troubleshooting, analytical, organizational, and communication skills.
• Ability to manage multiple projects and priorities simultaneously.
• Strong English reading, writing, and verbal communication skills.
• On-site position; not remote.

Responsibilities

• Serve as the primary administrator and technical expert for MasterControl Mx, MES, and eDHR.
• Manage system access, user roles, permissions, monitoring, maintenance, and troubleshooting.
• Configure and optimize workflows, electronic forms, system settings, and manufacturing processes.
• Support system validation, software updates, new modules, integrations, and system enhancements.
• Partner with Engineering, Quality, and Production teams to implement automation and process improvements.
• Provide end-user support and develop system training materials and documentation.
• Ensure employees follow applicable SOPs and system requirements.
• Maintain compliance with cGMP, FDA, ISO, change-control, and data-integrity requirements.
• Support audits by providing system documentation, reports, and evidence.
• Develop reports and dashboards to monitor manufacturing quality, efficiency, and KPIs.

Skills

Regulated manufacturing

System administration

GxP experience

SOP compliance

Documentation skills

Education

Engineering degree (BSc/MSc)

Tools

MasterControl Mx

API Integrations

Job description

Cirtec Medical Corporation seeks a Manufacturing Systems Administrator to manage MasterControl Mx, MES, and eDHR in a regulated manufacturing environment. You will ensure data integrity, regulatory compliance, and continuous improvement while partnering with Engineering, Quality, and Production teams.

The role emphasizes system validation, updates, and training material creation, with on-site responsibilities and a focus on cGMP and ISO standards.