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The HRIS Analyst provides hands-on Workday administration, configuration, reporting, data management, integration monitoring, and user support. Working within governance and change-control standards established by the HRIS Manager, the Analyst administers assigned functional areas, translates approved requirements into controlled changes, supports releases and implementations, and resolves Tier 1 and Tier 2 issues. The Analyst develops transaction instructions, validation rules, and technical support for basic Workday data entry performed by the HR Coordinator and other approved users; complex corrections, mass loads, security, configuration, and production changes remain with HRIS. The role also...
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The Senior Project Manager leads complex, cross-functional new product development projects for in vitro diagnostic (IVD) assays and diagnostic instrument systems in an FDA-regulated medical device environment. This role is accountable for project planning and execution from concept through launch, with emphasis on design control compliance, schedule, risk, resources, budget, dependencies, and clear decision-making. The Senior applies deep project management experience to anticipate and resolve complex issues, align cross-functional stakeholders, and drive timely decisions and escalations with limited oversight. The Senior Project Manager partners with R&D, Regulatory Affairs, Quality, Clinical Affairs, Operations, Marketing, and external development partners...
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The Logistics Manager is responsible for overseeing all inbound and outbound transportation activities, ensuring efficiency, complaint, and cost-effective movement of goods to and from the organization. This role leads shipping operations, manages carrier relationships, and coordinates inbound logistics from suppliers in partnership with Procurement to support uninterrupted supply and customer fulfillment. The Logistics Manager serves as the primary owner of logistics-related customer issues, including shipment delays, damages, cold chain, documentation errors, and delivery discrepancies. This role drives root cause analysis and implements corrective actions to improve service levels and...
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The Field Support Specialist I is primarily responsible for the formal technical training, validation assistance and implementation support of Meridian’s molecular and UBT platforms within the assigned geographical region. Responsibilities also include answering product and instrument related technical questions from customers, the sales force, and domestic and international distributors as needed. Additional duties may include conducting product demonstrations at customer labs, instrument set up and software upgrades, preparing and presenting topics to hospitals or laboratories, and training and validation support for immunoassay product lines as needed.
Candidate must reside in territory: Chicago...
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Account Executive is a sales professional responsible for leveraging their knowledge of company products and services to sell into new accounts and/or expand existing accounts. Manages customer inquiries and resolves issues. Meets or exceeds sales growth goals as determined by sales management.
Candidate must reside in the territory which includes illinois and Wisconsin
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Der Supervisor Filling & Finishing (m/w/d) übernimmt die fachliche und disziplinarische Verantwortung für den Bereich Abfüllung und Verpackung. Die Position stellt einen effizienten, qualitätsgerechten und termingerechten Produktionsablauf sicher, optimiert Prozesse und führt das Filling & Finishing-Team unter Einhaltung der geltenden Qualitäts-, Sicherheits- und Reinraumstandards.
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Primary role is to design and execute experiments, draw conclusions, and make data-driven decisions.
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The Scientist, Upstream Process Development is a hands-on technical role within Technical Operations and Development to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native/viral antigens, monoclonal antibodies, polyclonal antibodies, blockers, and custom manufacturing. This position develops, optimizes, characterizes, and scales upstream processes used to produce viral antigens and recombinant proteins, with a primary focus on mammalian cell culture. The Scientist will translate laboratory processes into robust, reproducible, and cost-effective manufacturing workflows; troubleshoot existing processes; and support technology...
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The Senior Manager of Sourcing and Procurement leads procurement and category management activities for the Cincinnati Diagnostics site, ensuring the reliable, compliant, and cost-effective acquisition of components, supplies, services, and equipment. This role collaborates across Operations, Production Planning, Quality, Finance, Engineering, and other functions to optimize supplier performance, mitigate supply risk, manage inventory, and control costs. The position establishes and maintains site purchasing and supplier-management practices, contributes to companywide procurement policies and standards, supports other Diagnostics sites as priorities and capacity allow, and partners with the Life Science...
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The Project Manager leads cross-functional new product development projects for in vitro diagnostic (IVD) assays and diagnostic instrument systems in an FDA-regulated medical device environment. This role is accountable for project planning and execution from concept through launch, with emphasis on design control compliance, schedule, risk, resources, budget, and clear decision-making. The Project Manager partners with R&D, Regulatory Affairs, Quality, Clinical Affairs, Operations, Marketing, and external development partners to achieve business and product objectives. The position may be based locally in Cincinnati or performed remotely, with travel as required to support project teams and key milestones.
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Responsible for supporting regulatory activities regarding released product, including, MDR investigations submissions, post market risk assessments (HHA), supports maintenance of the product Technical File in support of CE Marking, and risk management file updates. Leads field safety corrective actions/recalls, as required. Serves as a liaison between QA and manufacturing, R&D, customer service, and customers regarding complaint investigations, the identification of root cause, and the recommendation/coordination of Corrective/Preventative Action(s), when required.
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Provide quality engineering support to ensure the quality of design, sourcing and manufacturing of products at Magellan meets or exceeds all internal and external requirements and standards. Proactively participate in product development teams as the Quality core team member. Develop, establish, and maintain well-established quality engineering methodologies, systems and practices to meet customer and regulatory requirements.
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The Assembler position requires the employee to learn how to safely assemble, manufacture, and package regulated medical devices and kits in a performance driven environment under the supervision of higher-level operators / Supervisors / Managers. The employee will work to understand and meet all quality standards and adhere to all cGMP standards.
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The Senior Manufacturing Engineer provides broad, hands-on engineering support for diagnostic manufacturing operations. This position focuses on resolving complex production issues, improving equipment and process performance, and leading cross-functional automation, operational-efficiency, and capital-equipment projects.
The role applies mechanical, electrical, automation, controls, and process-engineering knowledge to maintain reliable manufacturing operations and implement sustainable improvements. The Senior Manufacturing Engineer also supports the...
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The Manager, R&D will be responsible for driving creation of a pipeline of new products/assays that will enable company growth within the POC primary care market (Pediatric, OB/Gyn & Family Practice) as well as assays complementary to the lead platform, i.e., other heavy metals.
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The Assembler position requires the employee to learn how to safely assemble, manufacture, and package regulated medical devices and kits in a performance driven environment under the supervision of higher-level operators / Supervisors / Managers. The employee will work to understand and meet all quality standards and adhere to all cGMP standards.
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Responsible for selling technical diagnostic products to laboratories via telephone as part of a specialty point of care team assisting in meeting and exceeding the sales and growth goals as determined by sales management. The position requires a high degree of organization and communication skills. The position must provide coverage and develop the best possible market penetration to existing and prospective accounts in an assigned territory using phone calls, emails, letters, faxes, and other company resources. Expectation is to meet and exceed sales and call goals. Individual must be able to relocate and transition into a field representative - Account Executive (AE) or Regional Point...
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The Manager, Clinical Operations is a seasoned professional with wide-ranging experience and a thorough understanding of clinical study management, biospecimen acquisition, FDA and ICH regulations and Good Clinical Practices (GCP). The candidate must be self-motivated, able to work and lead in a remote team environment and be able to establish strong, positive relationships with both internal departments, external clinical study sites and biospecimen vendors.
The successful candidate contributes to the...
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The Regional Point of Care Specialist (RPOCS) is a results-oriented professional responsible for driving growth and achieving sales plan in the LeadCare and other rapid point of care diagnostic product lines within assigned region.
Territory will cover: TX, LA, OK, AR, MS
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The Software Engineer with a focus on Cybersecurity will play a critical part in ensuring that software integrated into our diagnostic platforms meets cybersecurity, regulatory, and quality requirements. This system-level engineering role will facilitate software development, cybersecurity testers, and regulatory functions, ensuring secure design and compliant documentation throughout the product lifecycle.