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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.
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.
The Project Manager is responsible for reviewing project requirements, developing schedules, coordinating with teams, managing budgets, problem-solving, and ensuring compliance with contractual agreements. The role involves regular project reporting and completion verification while liaising with various stakeholders.
The Process Engineer will provide engineering and troubleshooting support for process equipment, lead new equipment installations, manage process improvements, and ensure compliance with safety and regulatory guidelines. They will also coordinate projects, interface with various teams, and oversee validation activities in a FDA-regulated environment.
Operating Engineer responsible for operating, maintaining, troubleshooting, and repairing engine room equipment in FDA-regulated industries. Must have a technical degree and 5-9 years of experience in utility operation and maintenance.
Serve as a focal point for Facility commissioning & qualification (C&Q) and computer system validation (CSV) in support of the delivery of capital projects. Manage project goals within scope, on budget, and on schedule. Develop C&Q/CSV strategies, review documents, and execute for special projects. Communicate progress with stakeholders and senior management.
The Project Manager at Mentor Technical Group (MTG) is responsible for leading projects from requirements definition through deployment, managing project teams, coordinating resources, establishing client relationships, and reporting project outcomes. They must have a strong educational background in computer science or engineering, a Bachelor's degree in Engineering, Sciences, or Business Administration, and 10+ years of project management experience with proven success.
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