Location : Fort Worth Texas Small Description: The Retail & Event Associate supports daily museum operations and private events at the American Airlines C.R. Smith Museum. This part-time role focuses on delivering exceptional guest experiences through retail support, visitor engagement, and on-site event hosting while representing the Museum professionally and contributing to its mission of preserving aviation history.

Location : Fort Worth TX Small Description: The Project Manager – Facility Maintenance Transition will lead the full transition of facility maintenance responsibilities to the airport authority, ensuring a smooth transfer of processes, scope, and operational knowledge. This role requires strong leadership, strategic planning, and cross-functional coordination to manage stakeholders, mitigate risks, and ensure continuity of facility operations throughout the transition period.

Location (mandatory): Princeton NJ USA 08541 The Corporate Meeting Planner plays a vital role in the organization by sourcing event venues, negotiating and executing contracts, and managing vendor payment processes for meetings, conventions, and global travel operations. This position works closely with Strategic Business Units (SBUs), Functional Centers of Excellence (FCEs), and travel stakeholders to lead all phases of meeting, convention, and business travel procurement. Responsibilities include managing Requests for Proposals (RFPs), Requests for Quotes (RFQs), and Requests for Information (RFIs) throughout the procurement lifecycle for both meetings and corporate travel-related services.

Location: Westborough, MA, 01581 The Compliance Specialist will perform critical QA tasks in support of GMP and non-GMP manufacturing programs and Regulatory Submissions at AIRM. This role ensures data integrity, quality, and compliance across a broad range of Quality Assurance areas, working closely with team members to maintain high-quality standards and value delivery for patients.

Location (mandatory): Bridgeport, NJ 08085 Provide administrative and operational support for logistics, trade compliance, and site operations by maintaining organized physical and digital filing systems and ensuring accurate, timely document flow. Review import/export documentation for compliance, support audits and inspections, and assist with shipping, receiving, and inventory records. Coordinate with warehouse staff, carriers, and freight forwarders to align shipment documentation and track status updates across teams. Utilize Microsoft Office and ERP systems.

Location (mandatory): Colorado Springs, CO 80915 provides day-to-day support for the Document Control and Production Planning teams within manufacturing operations. Approximately 90% of the role focuses on Document Control tasks, including scanning, organizing, and preparing documentation used by Manufacturing and Test. The remaining 10% of the role supports routine Production Planning activities such as updating standard reports or assisting with basic order scheduling and release processes.

Location : OAKBROOK TERRACE Illinois The Bilingual Spanish Call Center Supervisor is responsible for overseeing daily operations and performance of customer service representatives, including seasonal and temporary staff. This on-site role focuses on coaching, mentoring, scheduling, and performance management to ensure service levels, quality standards, and productivity goals are consistently met in a fast-paced call center environment.

Location : Washington District of Columbia The Project Management Analyst (PMA) provides essential support to multiple Project Managers within the Transmission & Distribution Program Management Office (T&D PMO) at PHI. The role focuses on business analysis, contract and financial administration, and program tracking to ensure successful execution of electric utility transmission and distribution projects.

Location: Davie, FL 100% Onsite Recent Master’s graduate master’s degree in engineering, Computer Science, Life Sciences, or related field. Min 3 years’ experience in pharmaceutical or regulated manufacturing; out of which 2 years in quality organization Min 3 years hands-on CSV experience reviewing and approving validation documentation. Direct experience supporting manufacturing or utilities systems (not just lab systems).