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Supervisor, Incoming Inspection, East Coast

Quidel Corporation

ROCHESTER, NYJobSeen todaySeen in employer's feed today

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At a glance

Compensation
No compensation found
Location
ROCHESTER, NY
Work Authorization
Not specified

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Job overview

QuidelOrtho seeks a Supervisor, Incoming Material Inspection to lead incoming inspection activities across East Coast operations. The role oversees a team and inspection processes for materials supporting manufacturing, ensuring quality and regulatory compliance, inspection readiness, and alignment with global standards. The supervisor partners with cross-functional teams, develops talent, and drives consistent execution and continuous improvement. The position can be based in Rochester, Athens, or Pompano.

Skills & qualifications

RequiredNice to have

Skills

Team LeadershipCoachingResource AllocationIncoming InspectionSampling Plans

Full job description

The OpportunityQuidelOrtho 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, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic.Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.The RoleAs we continue to grow as QuidelOrtho, we are seeking a Supervisor, Incoming Inspection East Coast. The Supervisor, Incoming Material Inspection - East Coast is a people leader within QuidelOrtho' s Global Quality & Compliance (GQ&C) organization, responsible for leading Incoming Material Inspection activities across East Coast operations. Reporting to the Manager, Incoming Material Inspection, this role ensures effective execution, oversight, and continuous improvement of incoming inspection processes to support manufacturing, protect product quality, and maintain QuidelOrtho' s Right to Operate. This leader provides operational leadership for the East Coast Incoming Inspection team, ensuring that raw materials, components, and consumables meet defined quality, regulatory, and technical requirements prior to release for manufacturing. The Supervisor partners cross-functionally with Manufacturing, Supply Chain, Supplier Quality, and other stakeholders to ensure alignment to global standards while addressing site-specific needs.The role ensures compliance with global regulatory requirements (ISO 13485, FDA 21 CFR 820, IVDR, and other applicable standards), while driving consistency, efficiency, and inspection readiness across East Coast operations. This position plays a critical role in translating global strategies and standards into effective local execution. In addition, this leader is responsible for developing talent, strengthening technical and compliance capabilities, and fostering a culture of accountability, engagement, and continuous improvement. Through strong leadership, data-driven decision-making, and collaboration, the Supervisor ensures high-quality execution and sustainable business outcomes. This position can be in Rochester, Athens or Pompano.The Responsibilities * Lead, coach, and develop a team of Quality professionals to ensure strong performance, engagement, and capability building. * Set clear priorities, manage daily operations, and allocate resources to meet business and compliance needs. * Foster a culture of accountability, speak-up, and continuous improvement aligned with GQ&C principles. * Ensure effective execution of incoming inspection processes for raw materials, components, and consumables supporting East Coast manufacturing sites. * Ensure timely and compliant material disposition to support manufacturing without compromising quality. * Execute inspection strategies, sampling plans, and acceptance criteria in alignment with global standards. * Ensure adherence to global regulatory requirements (ISO 13485, FDA 21 CFR 820, IVDR, and applicable standards). * Maintain a state of inspection readiness and support internal audits, regulatory inspections, and notified body engagements. * Ensure accurate and compliant documentation, data integrity (ALCOA+), and traceability within the QMS. * Partner with Manufacturing, Supply Chain, Supplier Quality, R&D, and Regulatory Affairs to ensure material quality requirements are defined, understood, and met. * Support supplier-related activities including material qualifications, changes, deviations, and investigations

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