Search the 29 jobs at Mentor Technical Group

Responsible for managing procurement activities specific to laboratory supplies and equipment, sourcing suppliers, negotiating purchase terms, ensuring timely deliveries, and resolving supply issues. Works closely with laboratory teams to procure materials and services, evaluate suppliers, and maintain accurate inventory records. Complies with company policies and regulatory standards related to laboratory procurement and provides support to laboratory staff in procurement process.

Supervise environmental maintenance services in pharmaceutical and biotechnology manufacturing areas, ensuring compliance with cGMPs and quality standards. Lead environmental monitoring and sampling processes, train new staff, and collaborate with cross-functional teams to maintain a clean GMP environment.

Documentation Specialist at Mentor Technical Group (MTG) responsible for driving and facilitating the change, approval, and release of documentation according to project schedules. Monitors configuration and documents changes management process effectiveness. Implements and maintains documentation and configuration assurance processes. Communicates documentation status to various levels of the organization. Participates in special projects and assists in departmental process development.

Support incident investigations, lead compliance with regulations, conduct safety trainings, issue safety talks, and coordinate EHS programs. Conduct risk assessments, perform audits, make recommendations for hazard control, and evaluate management of change. Requires a Bachelor's degree in Science or Engineering and a minimum of 5 years of related experience in Medical Devices & Diagnostics Pharmaceutical and/or Consumer industry.

Experienced C&Q Specialist with 5 to 8 years of experience in Commissioning and Qualification of utilities in the FDA-regulated industry. Responsible for managing multiple tasks, developing protocols and documentation, ensuring compliance, and risk assessments. Must have strong communication skills and a customer-focused approach.

Participate in activities related to documentation, administer electronic documentation system, maintain professional and technical knowledge, and contribute to team efforts in a life science engineering company serving FDA-regulated industry.

Responsible for the development and execution of Computer System Validation (CSV) and Decommissioning deliverables for Laboratory Equipment/Systems. Acts as the on-site project leader to plan, execute, and complete control systems projects. Coordinates communication with the client sponsor during all project phases. Requires a Bachelor's degree in relevant disciplines and a minimum of 8 years of experience validating laboratory computerized systems in a manufacturing environment.

Responsible for ensuring compliance with safety regulations and implementing risk-reduction strategies in the pharmaceutical and medical device industry. Conducts safety trainings, assessments, and audits to maintain a safe work environment. Coordinates EHS programs and manages change evaluations. Requires 5 years of experience and a Bachelor's degree in Science or Engineering.

Lead compliance specialist responsible for overseeing customer contract reviews, tracking services compliance, and ensuring adherence to regulatory requirements. Manage internal and external audits, generate compliance documents, and act as a point of contact for compliance requests. Requires 3-10 years of compliance experience in a manufacturing environment.

The C&Q Specialist at Mentor Technical Group (MTG) is responsible for commissioning activities, managing chemicals, risk assessments, and ensuring compliance with regulations in the life sciences industry. This role involves working with equipment, systems, utilities, and manufacturing processes for pharmaceutical, biotech, and medical devices.

Ensure accountability, transparency, and effective communication within the EHS Department. Investigate incidents and prepare reports. Maintain a safe work environment for all employees. Conduct safety audits and inspections to ensure compliance with regulatory agencies. Serve as primary contact for regulatory agencies. Keep abreast of safety and environmental law changes. Promote excellent relationships with clients and team members.

The Handyperson at Mentor Technical Group is responsible for conducting general repair work on buildings, mechanical, and electrical systems. They also assist with the upkeep of facilities and perform skilled repair activities. This role involves reading blueprints, assisting in equipment movement, and ensuring safety regulations are followed.

Perform start-up, operation, and shutdown of equipment, systems, and the plant in accordance with approved plant procedures. Operate coal handling equipment & general labor duties including cleaning. Observe and monitor equipment operation and maintain the facility to meet coal requirements. Assist in facilities maintenance activities.

Compile information, track requisitions, prepare purchase orders, run supplier qualification program, collaborate with various teams to advance workflow documents.

Conduct general repair work on buildings, mechanical, and electrical systems. Perform highly skilled repair activities and maintenance tasks. Read blueprints and assist with the movement of equipment and fixtures. Adhere to Health and Safety regulations. Other duties as assigned.

Conduct general repair work on buildings, mechanical, and electrical systems, diagnose problems, perform equipment repair, assist with equipment movement, and ensure compliance with Health and Safety regulations in facilities maintenance roles.

Lead the review and administration of customer contract reviews as it pertains to quality and compliance requirements. Develop and maintain a system for tracking services compliance. Accountable for compliance with international, federal, state, and local regulatory requirements. Act as a point of contact for customers, suppliers, and internal employees with regard to all contracts and compliance requests.

Ensure compliance with health and safety regulations, conduct training, audit programs, maintain documentation, and lead EHS qualification programs for contractors in the pharmaceutical industry.

Responsible for delivering and maintaining automation-based systems and solutions for Biopharmaceutical manufacturing in a GMP regulated environment. Support daily operations, continuous improvement, and projects for various automated equipment and control systems.

Provide training and audit services related to Environmental Management and Compliance for a world leader in life science engineering and technical solutions. Conduct internal audits and inspections to ensure compliance with regulatory requirements. Document and report findings to the Environmental Manager. Requirements include a Bachelor's degree.