Jobs at Mentor Technical Group

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

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.

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.

Own and manage deviations end-to-end in FDA-regulated sterile/aseptic environments: document, investigate root cause, implement CAPA, track trends, report to management, support audits, and optimize SOPs.

Provide administrative support including meeting coordination and minutes, travel arrangements and expense processing (Concur), onboarding new hires, office supply and procurement support (Ariba), event planning, and general office administration.

The Project Manager will oversee project management deliverables, global communications, and monitor project plans in the FDA-regulated industry.

The EHS Specialist ensures workplace safety across regulatory compliance within the FDA-regulated industry, provides training, investigates incidents, and maintains EHS documentation.

The EHS Specialist ensures compliance with safety regulations, conducts training, investigates incidents, and maintains EHS documentation and reporting.

The EHS Specialist will ensure compliance with environmental, health, and safety regulations, conduct training, monitor regulations, and promote a safe working environment across multiple client sites in Puerto Rico.

As a Supply Chain Manager, the role ensures compliance with cGMP, oversees material handling, collaborates on logistics, and manages forecasts and production schedules. Responsibilities include stakeholder communication, compliance with regulations, and evaluation of operational procedures for efficiency and improvement.

Lead the technical strategy for robotics and automated storage, ensuring reliable integration and operational readiness while managing system architecture, performance, and compliance with safety standards.

Perform repair work on facilities systems, maintain health and safety regulations, operate high-pressure equipment, and assist with moving equipment and supplies.

Provide technical support for pharmaceutical manufacturing by overseeing commissioning and qualification activities, ensuring compliance with regulatory standards, and managing documentation related to equipment and systems.

Engineer to solve technical problems, perform operational audits, and collaborate on equipment and system modifications with various departments.