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The EHS Specialist is responsible for ensuring health, safety, and environmental compliance in a regulated pharmaceutical environment. Duties include contractor management, regulatory compliance, safety training, waste management, and engaging with regulatory agencies. This role requires strong communication and problem-solving skills, along with a thorough understanding of EHS regulations.
The CSV Specialist at Mentor Technical Group oversees asset/system decommissioning, validation activities, and documentation management in compliance with industry standards. Responsibilities include investigating customer complaints, developing and executing validation protocols, and managing technical issues while promoting client relationships and ensuring quality documentation.
As an EHS Specialist at Mentor Technical Group, you will be responsible for ensuring compliance with health, safety, and environmental regulations in a regulated pharmaceutical facility, overseeing contractor management, waste management programs, and acting as the primary contact for regulatory inspections.
The MRO Specialist is responsible for designing and socializing MRO global business processes. Key tasks include data mapping, data migration support, executing UAT strategies, and creating training content. Additional responsibilities encompass technical protocol generation and review of data mapping processes.
The Compliance Specialist will ensure compliance with safety and efficacy guidelines in the FDA-regulated industry by supporting the Facilities Team, managing the Contractor Safety Program, performing audits, monitoring compliance KPIs, and providing compliance training to associates and subcontractors.
The Process Engineer will provide engineering support and expertise for process equipment and utilities, driving improvements and managing installations. Responsibilities include troubleshooting, project execution, and ensuring compliance with safety and quality standards. This role involves collaboration with various teams on new equipment design, project management, and adherence to regulatory guidelines.
The Process Engineering Manager oversees engineering support for process equipment in the FDA-regulated sector, ensuring compliance with safety regulations. Responsibilities include troubleshooting, managing equipment installations, leading process improvements, and collaborating on project execution and validation activities.
The Automation Engineer will deliver and maintain automation systems for biopharmaceutical manufacturing. Responsibilities include providing automation support for daily operations and projects in a GMP environment, designing and configuring control systems, and managing technical changes.
The Data Analyst will create scorecards, dashboards, and reporting tools. Responsibilities include writing and maintaining reports, designing custom reports, and collaborating effectively with team members. A bachelor's degree and at least one year of experience are required.
The CMMS Specialist is responsible for managing and documenting maintenance work orders, ensuring compliance with regulations, and overseeing vendor activities on-site. The role involves troubleshooting lab equipment, performing physical inventory, and supporting calibration and maintenance tasks for instrumentation. Strong technical writing, organization, and interpersonal skills are essential, along with the ability to work independently.
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