Role Description Our Quality Assurance & Center of Excellence team at Arise is looking for a Manager, Performance Excellence who will be responsible for assessing the quality and adherence to compliance. The job responsibilities include: - Providing clear insight into performance drivers and the levers which impact performance. - Leading and managing calibration sessions, ensuring all quality analysts meet or exceed the client required 90% calibration threshold. - Owning on-time, accurate, quality analysis and reports/visualizations in tight alignment with specified project objectives. - Collaborating & communicating effectively with business sponsors, executives, and stakeholders. - Exhibiting strong analytical and problem-solving skills; thriving on change and possessing an inquisitive mind. - Structuring data analysis, driving analytics insights and analytical solutions. - Making recommendations to management regarding the development of policies and procedures; identifying and implementing processing efficiencies; identifying trends and continuing education opportunities. - Providing program and agent performance reporting, including statistical analysis and reporting. - Maintaining proper documentation of call performance and associated corrective measures as applicable. - Monitoring team compliance to quality standards using established audit procedures. Qualifications - Minimum 5 years working experience in a quality Lead role or its equivalent. - Thorough understanding of quality management framework. - Excellent written and verbal English communication skills. - Experience in preparing and presenting written project status reports and executive briefings. - Demonstrated ability to develop analytical insights and summarize complex problems into concise reports and findings. - Proficiency in MS Excel, Word, and PowerPoint. - Demonstration of strong time and work management skills with a progressive, people forward attitude. Benefits - Work-from-home flexibility. - Opportunity to be part of a revolutionary company. - Collaborative and innovative team environment.

Role Description The IT Integrator will support the following activities: - Software Testing - Development of Test Cases - Problem Solving - Content Management - Software Development - Sustainment in support of NTMPS and its applications, and MYNAVY HR IT SOLUTIONS Responsibilities include: - Coordinating system integrations between applications/platforms - Managing interface dependencies and data flows - Supporting migration and cutover activities - Troubleshooting integration and connectivity issues - Validating end-to-end functionality after deployments - Coordinating across infrastructure, development, security, and business teams - Supporting configuration management and environment synchronization - Assisting with requirements analysis and technical documentation - Monitoring integration performance and operational stability - Supporting change management and release activities - Facilitating testing, validation, and defect resolution - Ensuring compliance with operational and security standards - Providing technical advisory support to stakeholders and leadership - Assisting with vendor/contractor coordination - Supporting process improvement and operational modernization efforts - Other duties as assigned Qualifications - High school diploma or GED - 6+ Years of relevant technical experience - 2+ years of recent (within the last four (4) years) IT Integration Experience - Experience with the Navy and the Fleet Training Management and Planning System (FLTMPS) is preferred - Experience with SQL - Background check - Knowledge of software testing methodologies, including functional, regression, integration, and performance testing - Knowledge of software development life cycle (SDLC) and Agile methodologies - Ability to analyze requirements and identify gaps, risks, and potential defects early in the development process - Excellent verbal and written communication skills Benefits - A broad range of benefits - Opportunities for professional development - Well-being programs - Flexibility to make daily choices for a healthy work-life balance - Positive and supportive culture - Celebration of individual uniqueness Company Description Chenega MIOS is led by a purpose to make an impact that matters, focusing on education, giving, skill-based volunteerism, and leadership to drive positive social impact in communities.

• Define and execute the global supply chain strategy for biosimilars across DS, DP and finished products • Lead integrated business planning (IBP / S&OP) and translate strategy into actionable supply plans • Ensure reliable supply by managing internal manufacturing sites and external CMO partnerships • Drive demand, capacity, and inventory planning across a complex global network • Secure launch readiness and lead lifecycle supply management, including tech transfers and product changes • Oversee logistics, distribution, and cold-chain operations to ensure high service levels • Manage supply chain risks and develop mitigation strategies for capacity and sourcing constraints • Drive financial performance through cost optimization, inventory management, and KPI governance • Build and lead a high-performing global supply chain organization • Collaborate cross-functionally with R&D, Quality, Manufacturing, Commercial, and Finance

Title: Clinical/Commercial Supply Chain Senior Manager- CONTRACT Location: Needham, MA Job Description: Clinical/Commercial Supply Chain Senior Manager- CONTRACT - Hybrid role (3 days a week) Needham, MA - Contract until December 31,2026 - Salary: $160-$180k annualized Position Overview We are seeking a talented, self-driven, and highly motivated Clinical/Commercial Supply Chain Manager/Senior Manager with deep expertise in supply chain management. This role is responsible for overseeing the end-to-end supply of Clinical Trial Materials (CTM) across all stages of clinical development, as well as commercial operations in the future, including packaging, labeling, and distribution. The position will also serve as a key partner to Clinical Operations, Regulatory, Quality, and clinical sites, providing guidance on all aspects of CTM, comparators, and supplemental products, as applicable.Key Responsibilities - Support clinical/commercial supply activities for ongoing and new clinical trials or commercial launch to ensure on-time delivery, including demand forecasting, trial monitoring, resupply planning, IRT or inventory system setup, and distribution. - Lead the design and execution of packaging and labeling campaigns, including timeline management, documentation review/approval, and coordination with Contract Development and Manufacturing Organizations (CDMOs). - Manage CDMO relationships and provide comprehensive oversight of clinical or commercial supply activities. - Ensure uninterrupted supply of clinical trial materials for studies across U.S. and international (ex-U.S.) sites. - Support timely startup of new clinical studies by ensuring availability of required materials. - Oversee and track manual distribution activities to global clinical sites, ensuring on-time delivery. - Develop and maintain efficient processes and tracking tools for manual shipments. - Review clinical protocols and develop appropriate supply chain strategies. - Manage logistics operations, including inventory control, import/export activities, transportation, and third-party warehousing. - Act as a cross-functional liaison for inventory and distribution activities, including scheduling, issue resolution, change management, and vendor oversight. - Drive timelines for bulk manufacturing, packaging, labeling, and final release to meet forecasted demand. - Develop, maintain, and present Supply Chain dashboards to senior leadership. - Partner with Accounts Payable and Legal to ensure timely processing and approval of purchase orders, change orders, and invoices related to CDMOs. - Collaborate effectively with cross-functional teams, including Clinical Operations, Pharmaceutical Sciences, Quality Assurance, and Regulatory Affairs. NOTE: This person must be able to lift 80 to100 lbs as this will be a requirement on handling shipments.Preferred Qualifications - Bachelor’s degree with 8-10 years of experience in supply chain planning within the biotechnology or pharmaceutical industry; PMP certification is a plus. - Strong project management, organizational, and communication skills. - Ability to thrive in a fast-paced, innovative environment while remaining flexible, proactive, and resourceful. - Experience managing contract packaging and labeling vendors (strongly preferred). - Knowledge of regulatory requirements for clinical/commercial supply distribution across the U.S., APAC, and EU, including testing and labeling standards. - Experience with cold-chain logistics and shipping validation is a plus. - Solid understanding of cGMP, GCP, GDP, and global transportation regulations for pharmaceutical materials. - Experience working with Qualified Persons (QP), IRT systems, depots, and global CTM distribution. NOTE: This person must be authorized to work in US. We are unable to accommodate any sponsorships.