• Preparation, development and maintenance of integrated project schedules for complex industrial and plant engineering projects across all project phases (from planning through execution) • Coordination and integration of sub-schedules from all project stakeholders (engineering, procurement, construction and external partners) into a consolidated master schedule • Execution of schedule control, including analysis of project progress, critical paths and deviations against the schedule baseline • Preparation of schedule and progress reports and communication of risks, opportunities and recommended actions to project management and the project team • Support for project management in scheduling strategies, change management and assessment of project impacts on milestones and the overall schedule • Application and further development of Lean methods and best practices in schedule management to optimize project workflows • Facilitation of scheduling and control workshops and serving as the central interface for all schedule planning matters within the project • Ensuring the quality, consistency and traceability of all schedule-related data and documentation

• A Direct Support Professional (DSP) caregiver provides direct support, positive direction, instruction, and assistance to individuals with mental, intellectual & developmental, and physical disabilities. • The ultimate goal is to empower individuals with disabilities to live as independently and comfortably as possible while maintaining their dignity and respect. • Provide hands-on assistance, encouragement, mentoring, and guidance. • Ensure the comfort, safety, and personal growth of the individuals we serve. • Assist with daily living tasks such as moving around, getting in and out of bed, dressing, bathing, toileting, personal hygiene and more. • Perform housekeeping and laundry duties

• Lead our wireless compliance strategy and drive the evolution of our global laboratory network • Oversee global SAR/RF exposure requirements (FCC, RED, carriers) • Advance automation across existing labs • Expand regulatory capabilities into new markets (e.g., Mexico) • Provide technical leadership to regional teams to support global client development

• Respond promptly to donor screening referrals by reviewing medical records, donor documentation, and Donor Risk Assessment Interview (DRAI) information. • Evaluate donor eligibility using established Ossium guidelines, clinical criteria, and available case information. • Identify missing, incomplete, or conflicting information and proactively obtain additional documentation or clarification from partner organizations as needed. • Make independent donor acceptance and deferral decisions within established guidelines, escalating complex or exceptional cases when appropriate. • Complete donor verification activities, required documentation, and internal notifications related to donor eligibility and case progression. • Create and maintain organized donor files, ensuring all supporting documentation is accurately recorded and readily accessible. • Track donor cases through recovery and shipping workflows, providing timely follow-up and status updates as needed. • Document all screening activities, eligibility determinations, partner communications, follow-up actions, and case outcomes in a timely and accurate manner. • Coordinate with OPOs, recovery partners, and internal stakeholders to ensure efficient case management and resolution of outstanding issues. • Monitor pending cases, complete follow-up activities, record final case dispositions, and communicate next steps to partner organizations. • Serve as a primary point of contact for partner organizations by providing professional, responsive support and addressing screening-related questions and inquiries. • Maintain current knowledge of Ossium policies, donor eligibility criteria, industry regulations, and operational procedures through ongoing training and education. • Develop familiarity with partner-specific processes, documentation practices, and terminology to support effective collaboration and consistent communication. • Contribute to process improvement initiatives and support the implementation of new workflows, technologies, and operational enhancements. • Commitment to maintaining confidentiality and handling sensitive medical information in accordance with applicable privacy and regulatory requirements.