Search the 32 jobs at Mentor Technical Group

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 Handyperson is responsible for conducting various repair and maintenance tasks under supervision, including mechanical and electrical systems work, painting and decorating, problem diagnosis, and equipment repair. Responsibilities also include following health and safety regulations, operating tools, and assisting with equipment movement and setup.

The Documentation Specialist will translate and maintain technical documents accurately, collaborating with experts to ensure compliance with relevant guidelines. Responsibilities include proofreading, managing translation activities, supporting document control, and adhering to regulatory requirements, while communicating effectively with clients and internal personnel.

The Documentation Specialist will translate documents, maintain accurate documentation, support document control activities, proofread and edit materials, and liaise with clients. The role requires collaboration with technical teams and management of translation activities to meet deadlines while adhering to regulatory standards.

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 Handyperson at Mentor Technical Group will perform general repairs on buildings and facilities systems, including diagnosing problems, executing repairs, and assisting with equipment movements. Responsibilities include painting, maintaining safety standards, and following verbal instructions under supervision.

The Project Control Specialist will support resource allocation, purchasing, and finance activities within the business unit. Responsibilities include managing purchase orders, invoicing, expense management, and providing support for project controls and metrics, while ensuring compliance with company policies and ethical standards.

The Perito Electricista will install, maintain, and repair electrical systems while ensuring compliance with relevant codes. Responsibilities include troubleshooting PLCs, programming VFDs, conducting inspections, documenting operational parameters, and maintaining safety and regulatory standards. Emergency response and overtime may be required.

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 Process Development Scientist is responsible for designing and executing scientific experiments, analyzing data, and developing new protocols. They ensure compliance with protocols and guidelines, represent the department in project teams, and may mentor others. The role involves extensive data analysis, literature review, and collaboration within and outside the company.

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 C&Q Specialist will oversee the commissioning and qualification of utilities, develop various protocols, and manage compliance with pharmaceutical safety guidelines. The role requires strong communication skills and the ability to handle multiple tasks independently while ensuring proper management of chemicals and equipment decommissioning.

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.

Responsible for the implementation of small Capital/Expense Project

The QA Specialist will manage investigations related to pest control, finalize root cause investigations and CAPAs, ensure compliance with FDA and GMP guidelines, provide coaching for colleagues, and analyze CAPA effectiveness to prevent recurrence.

The EHS Specialist is responsible for ensuring compliance with health, safety, and environmental regulations within the pharmaceutical sector. This role involves reviewing contractor documentation, conducting training, performing safety observations, maintaining reporting standards, and leading safety qualification programs for contractors.

The C&Q Specialist is responsible for conducting commissioning and qualification activities, managing chemical substances, performing risk assessments, and ensuring compliance with cGMP requirements. Key tasks include preparing documentation such as protocols and reports in the pharmaceutical, biotech, and medical device sectors.