SGS_JOB_1061
Contract - 06 Months+
• This position will focus mainly on our FDA remediation efforts, with potential remediation assistance on other upcoming audit streams. • Temp to Perm • M-F on-site • Will manage people - manage multiple project managers 5-7 years’ experience • experience handling multiple projects/programs • PMP certification would be a plus • willing to come in, roll up their sleeves and take ownership of large projects. Program Manager II should have a sharp business mind and proven ability to strategize and implement high-level program initiatives across the global operations program/project portfolio. As a natural leader, this person should have strong talent for program/project coordination and delegation. Ultimately, the program manager should be motivated by a desire to optimize productivity and nurture program success from inception to completion. Programs could include but not limited to mergers and acquisitions diligence, integrations and divestitures, footprint optimizations, manufacturing transfers/capacity expansions, life-cycle management, product specific strategy programs, operations resilience, business continuity planning, capex management, site process/yield improvement and long-range capacity planning. This role will ensure the deliverables of the program are achieved on or ahead of schedule and within cost standards such that they meet the desired strategic objective (i.e. quality standard, value), business deliverable and/or key decision required. Employees should be able to strategize, implement, and maintain program initiatives that adhere to organizational objectives. They should develop program assessment protocols for evaluation and improvement, maintain organizational standards of satisfaction, quality, and performance. Oversee multiple project teams, ensuring program goals are reached. Manage budget and funding channels for maximum productivity. They typically lead teams or programs with broad visibility. They apply conceptual thinking to understand c
Location (mandatory): Franklin, TN Tariff Classification & Technical Research: Assign accurate HTS/Schedule B classifications for complex parts by researching engineering drawings and technical specifications to ensure full regulatory compliance. Compliance Auditing & Risk Mitigation: Conduct regular internal audits to identify compliance gaps, manage prior disclosures, and develop long-term process improvements to minimize financial and legal risks. Trade Legislation & Strategic Analysis: Monitor and analyze international trade laws and legislative changes (such as Section 301 or USMCA eligibility) to forecast economic impacts on company operations and supply chain flow. Cross-Functional Collaboration: Act as a central liaison between legal, finance, and supply chain teams to ensure trade strategies and compliance protocols align with broader corporate business goals. Executive Reporting & Decision Support: Synthesize technical trade data into high-level briefings and KPI reports for senior leadership to drive data-driven decisions regarding market entry and cost-saving opportunities. Operational Liaison: Coordinate directly with customs brokers, freight forwarders, and government agencies like CBP to resolve daily documentation discrepancies and shipment delays.
Location:- Tucson, AZ 85755 (Onsite) Responsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities to support Ventana projects. Exercises technical expertise and discretion in the design, execution and interpretation of experiments that contribute to project strategies. Prepares technical reports, summaries, protocols and quantitative analyses. Presents and discusses results of experiments within department and project team. Maintains high level of professional expertise through familiarity with scientific literature and may participate in conferences and professional societies. Follows company policies and procedures for GMP, GLP, Design Control and others as appropriate. Maintains complete and accurate laboratory documentation and electronic files. May act as principal investigator in conducting own experiments.
Location:- Pearl River NY 10965 This is a laboratory-based position within the Vaccines Early Bioprocess Analytical Development group. The individual will perform routine sample testing, analytical method development and assay qualification studies in support of early vaccine development. Assays include but are not limited to enzyme-linked immunosorbent assays (ELISAs) and other plate-based testing. This is a dynamic position that will require work on fast-moving and high-visibility projects.
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.