Effectively communicates verbally and in writing. Demonstrates a sense of urgency to complete production schedule on time. Accepts personal responsibility for the quality and timeliness of work. Accurately and timely completes all required reporting functions using an SAP/ERP computer system. Uses computer based documentation system to find, view and print specifications

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world leading in vitro diagnostics company with award winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurat

Assists with quarterly and year end tax provision information gathering for external preparation of provision calculations Prepares various calculations according to Internal Revenue Code and Treasury Regulations Prepares and timely files property tax reports, monthly and quarterly US state & local transaction tax reports and information reporting for payments made to ven

Work order creation and accompanying device history record paperwork to support manufacturing operations. Purchase order creation and maintenance. Retrieval and organization of work orders and device history record paperwork from manufacturing. SAP maintenance of open work and purchase orders as well as maintaining and updating documents via change control process in docu

Lead and/or support IT Audit initiatives to ensure controls are in place and are aligned with SOX compliance (primary focus) and in support of other compliance frameworks where appropriate. Administer and collaborate with owners (system, control, business, etc.) to ensure completion of user access and system and organization controls (SOC) reviews. Perform IT internal con

Leads efforts in managing the nonconforming material, process deviations, biological raw material testing, stability programs and customer complaint investigation functions Manages effective quality control systems through the identification, segregation, root cause analysis, corrective action, disposition and trending of product and process failures and inefficiencies Ma

Gather functional and non functional requirements and draft user stories using the Agile/Scrum methodology with acceptance criteria Define and articulate product features, configuration, specifications, and user stories Work with stakeholders, Project Managers and developers to ensure alignment with requirements Collaborate in an Agile environment with cross functional te

Member of the Global IT Supply Chain and Operations team, supporting the QuidelOrtho manufacturing facilities Actively works with Business Resources to determine the technical solution that best meets the business requirements for Manufacturing Order Execution and Inventory Management functionality. Explores and keeps up to date on current RF data collection and MES techn

Manufactures (i.e. Formulates bulks, and Quality Controls) products (i.e. Lateral flow devices, controls/calibrators and microtiter systems) while adhering to regulatory requirements and business polices /procedures and schedules Provides training to chemistry staff on Manufacturing Instructions and Standard Operating Procedures (SOP) Displays leadership by assessing issu

Maintains updated global market and competitive intelligence. Proactively develops and executes strategies based on competitive intelligence and appropriate market research and analysis. Collaborates with regional marketing teams and sales enablement to align global marketing plans in each region and define and track regional marketing and sales metrics. Works across Quid

Working collaboratively with the US Sales Organization, the Contract Manager will provide quotes and develop agreements, revising as needed throughout the negotiation process. Amend and restructure existing agreements when required. Track the status of new offers to measure win rates and cycle times. Ensure that all contracts are structured in accordance with Company poli

Manufactures (i.e. Formulates bulks, and Quality Controls) products (i.e. Lateral flow devices, controls/calibrators and microtiter systems) while adhering to regulatory requirements and business polices /procedures and schedules Provides training to chemistry staff on Manufacturing Instructions and Standard Operating Procedures (SOP) Coordinates the activities of the Che

Effectively communicates verbally and in writing. Demonstrates a sense of urgency to complete production schedule on time. Accepts personal responsibility for the quality and timeliness of work. Accurately and timely completes all required reporting functions using an SAP/ERP computer system. Uses computer based documentation system to find, view and print specifications

Maximizes customer retention rates by ensuring customer satisfaction, executing customer touchpoint/call plan, being single point of contact for all problem resolution, and anticipating and defending against competitive threats. Grows existing accounts and develops new accounts in order to meet seasonal and non seasonal revenue goals by establishing personal credibility,

Manages site compliance to EPA, APCD, OSHA, DEH, Life Safety Code, DTSC, and City and County regulatory and permitting requirements. Manages the collection, storage, and compliance reporting for all regulated waste activities, hazardous waste paperwork including manifests, training documentation, Source Reduction plan, Excluded Recyclable Materials Reporting and land bans