Jobs at Mentor Technical Group

Responsible for site EHS compliance, permitting, inspections, incident investigations, training, recordkeeping, and regulatory reporting (OSHA, EPA, AQMD, ADA, fire codes). Serve as primary regulatory contact, maintain permits and EHS program documentation, conduct ergonomic and safety training, support workers' compensation oversight, and drive corrective actions and management of change processes to minimize exposures and ensure continuous compliance.

Manage and maintain EHS compliance for FDA-regulated sites: conduct inspections, incident and near-miss investigations, regulatory reporting (air, water, waste), training, ergonomic programs, waste management, permit compliance, and serve as primary regulatory contact while promoting safety culture and corrective actions.

The CMMS Analyst manages a computerized maintenance administration system to ensure information flow, maintain records, develop reports, and train users. They handle data related to maintenance activities and metrics reporting.

Lead the Quality Management System compliance for clients in regulated industries, overseeing training programs, audits, and continuous improvement initiatives while ensuring effective communication and data analysis for quality enhancements.

Responsible for ensuring documentation compliance in a regulated environment, providing technical support, maintaining documentation accuracy, and fostering client relationships while adhering to regulatory standards.

The HR Associate will coordinate various HR functions including onboarding, record management, benefits support, and employee communications to ensure effective HR operations.

The Jr. C&Q Engineer will develop project schedules, monitor engineering progress, and ensure compliance with project deliverables in the life sciences industry.

This internship provides hands-on experience in HR functions like recruitment, onboarding, employee relations, and compliance in a dynamic organization.

The Maintenance Planner will schedule maintenance activities, ensure compliance with regulations, and improve workforce productivity through effective planning and coordination.

Support Commissioning and Qualification activities in pharmaceutical manufacturing, develop procedures, manage change controls, and troubleshoot issues.

Support EHS compliance for FDA-regulated life sciences sites: maintain regulatory permits and reporting, conduct incident and near-miss investigations, deliver training, manage waste programs, perform inspections and ergonomic assessments, and act as regulatory liaison to ensure OSHA, EPA, CAL/OSHA and other requirements are met.

The Sr. Compliance Specialist will manage asset lifecycle, calibrations, work orders, and environmental monitoring for FDA-regulated industries, ensuring compliance in life sciences.

Design, implement, and maintain LAN/WAN networks for FDA-regulated environments; monitor and troubleshoot performance and security; implement firewalls/VPNs; support compliance, documentation, audits, and cross-team integration to ensure reliable, secure network operations.

Assist in design, development, testing, and implementation of engineering solutions. Perform basic calculations, modeling, drafting, and prepare technical documentation. Collaborate with senior engineers to troubleshoot, participate in project meetings and site visits, ensure regulatory compliance, and support continuous improvement initiatives.

Plan and maintain production schedules, allocate resources, monitor project progress, identify bottlenecks, communicate updates, and support resource planning and compliance in regulated manufacturing environments.

Update and create facility drawings (architectural, mechanical, electrical, HVAC, P&IDs, control schematics) from redlines, sketches, and field inspections; maintain drawing database and revisions; produce layout scenarios; navigate layers to generate drawings/PDFs; ensure SOP-compliant approvals.

Lead packaging projects from design through implementation, coordinate cross-functional teams, conduct feasibility and cost analyses, manage timelines and budgets, ensure regulatory compliance, improve processes for efficiency and sustainability, and provide technical support for packaging issues.

Lead and support commissioning and qualification (C&Q) activities: author, review, and approve C&Q protocols and reports; execute commissioning; manage change controls and deviations; troubleshoot, perform root-cause investigations, and transfer technical knowledge across sites to ensure GMP and regulatory compliance.

The role involves leading technical strategy for robotics and ASRS integration, overseeing system design and governance to ensure performance, reliability, and compliance across OT/IT frameworks in industrial environments.

Plan, coordinate, and maintain production and resource schedules; monitor progress; resolve conflicts; report scheduling performance; communicate changes and support resource planning to optimize operations.