Meridian Bioscience

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Job Locations US-Remote
Achieve financial plan for territory or accounts assigned for the Life Science unit for both sales and operating income.  The Sales Director will lead the North America Life Science team to meet and exceed the company’s goals for sales and profits. This person will lead a team of sales individuals for effective account strategy implementation with key global accounts, consultative selling, and technical assistance for new & existing customers in the field of molecular and immunological testing. The successful candidate will maximize Meridian’s Life Science market share in existing and new accounts and sales opportunities by promoting product growth and providing development, management and account direction for the North America Life Science team and the assigned territory.
Company
Meridian Life Science, Inc.
Job Locations US-MA-North Billerica
Responsible for the advancement and accomplishment of Meridian’s strategic goals related to clinical evaluations and qualifications of in vitro diagnostic (IVD) assays of new or marketed devices in Dx platform area.  Manages multiple projects in different phases to obtain the expected results and gain maximum organizational benefit.  Contributes to and manages the local clinical strategy and operations at the manufacturing site. The Clinical Program Manager will be focused on blood chemistry. Manages a team of clinical professionals to conceptualize, develop and communicate clinical trial strategies as well as manage and participate in the execution of clinical trials and generation of reports for timely regulatory submissions. Ensures that all clinical studies within the program are being managed and conducted according to Good Clinical Practice (GCP) and other applicable regulatory requirements.
Company
Meridian Bioscience, Inc.
Job Locations US-OH-Cincinnati
Responsible for the planning, coordination and monitoring of Meridian’s safety and worker’s compensation programs across all U.S. sites to eliminate or reduce cost of illness and promote the maintenance of employee health and safety. Ensures compliance with all regulations and policies. Responsible for timely processing of workers' compensation claims; evaluates accident reports to determine accuracy and completeness and investigate claims. Provides training and guidance for the company on all U.S. EHS and Worker’s Compensation processes and procedures. 
Company
Meridian Bioscience, Inc.
Job Locations US-OH-Cincinnati
The Sr. Analyst, Global Diagnostics Financial Planning and Analysis (FP&A) will lead the monthly, quarterly, and annual financial planning, forecasting and analysis for the Diagnostics segment.  He/she will act as a business partner for managers and project leaders from various areas of the company, providing financial and business analysis support. He/she will lead and/or support various ad hoc projects, which may include profitability analyses of commercial and supply chain initiatives, strategic investments, risk management projects, M&A, capital investments, and other efforts to continuously improve the existing processes and support the key business activities.
Company
Meridian Bioscience, Inc.
Job Locations US-OH-Cincinnati
The immunoassay function within R&D is responsible for developing the next generation diagnostic kits for Meridian. The Senior Research Associate will support the development of a new diagnostic device as part of an assay team. Responsible for designing and executing experiments, acquiring data, drawing conclusions for discussion and recommendations. 
Company
Meridian Bioscience, Inc.
Job Locations US-OH-Cincinnati
The Production Worker (Para-Pak Operator I) safely manufactures FDA regulated medical devices in a fast-paced and results-oriented environment, meeting quality standards in accordance with cost, schedule and all standard cGMP operating procedures and guidelines.
Company
Meridian Bioscience, Inc.
Job Locations US-OH-Cincinnati
This position will be responsible for supporting Meridian’s regulatory and quality processes and ensuring that Meridian’s activities are consistent with applicable quality and regulatory requirements.  Assist with product compliance throughout all stages of the product lifecycle as well as work with cross-functional teams to provide support of business objectives. Also assist in assembling timely preparation of documents for domestic and international regulatory submissions, ensuring compliance with applicable regulations. 
Company
Meridian Bioscience, Inc.
Job Locations US-OH-Cincinnati
This position will be responsible for supporting Meridian’s regulatory and quality processes, including Meridian's product realization process, to ensure that Meridian’s activities are consistent with applicable international quality and regulatory requirements, especially the design, development and manufacture of medical devices. Assist regulatory affairs team with global product compliance throughout all stages of the product lifecycle, including research, development, transfer, validation/verification, labeling, regulatory submissions, and lifecycle maintenance.  Works cross-functionally to ensure that regulatory guidance is provided in support of international business objectives.
Company
Meridian Bioscience, Inc.
Job Locations US-MA-North Billerica
Responsible for leading projects supporting remediation and implementation of the quality design and risk management processes. Support the remediation and implementation of the post-market risk assessment process. Review and modify policy and operating procedures and provide effective solutions for success. Active involvement with the remediation of the Quality System Management.
Company
Meridian Bioscience, Inc.
Job Locations US-MA-North Billerica
Responsible for supporting post market regulatory activities regarding complaint analysis, MDR submissions, post market risk assessments (HHA), supports maintenance of the product technical file in support of CE Marking, and risk management file updates. Also leads field safety corrective actions/recalls, as required. Serves as a liaison between quality assurance and manufacturing, research and development, customer service and customers regarding complaint investigations, the identification of root cause and the recommendation/coordination of corrective/preventative action(s), when required.
Company
Meridian Bioscience, Inc.
Job Locations US-OH-Cincinnati
We are looking for a Senior Finance Analyst to join our team! This person will be responsible for preparation of all aspects of corporate financial reporting, including consolidated financial statements and business unit financial statements.  Administers financial and accounting consolidation system and assists in preparing financial reports filed with the Securities and Exchange Commission.  Ensures closing calendar is adhered to by business units.   
Company
Meridian Bioscience, Inc.
Job Locations US-MA-North Billerica
The Quality Assurance Manager is responsible for direct management of the Quality Control (QC), Quality Management System, and Quality Engineering functions. Will implement and maintain the quality program and associated procedures to ensure overall Quality Management System (QMS) compliance with the FDA Quality Standard Regulations (21 CFR Part 820), ISO 13485 and other local, state, and international regulations and laws, associated with maintaining a marketed medical device. 
Company
Meridian Bioscience, Inc.
Job Locations US-MA-North Billerica
The Quality Assurance Manager is responsible for direct management of the Quality Control (QC), Quality Management System, and Quality Engineering functions. Will implement and maintain the quality program and associated procedures to ensure overall Quality Management System (QMS) compliance with the FDA Quality Standard Regulations (21 CFR Part 820), ISO 13485 and other local, state, and international regulations and laws, associated with maintaining a marketed medical device. 
Company
Meridian Bioscience, Inc.
Job Locations US-OH-Cincinnati
The Machine Operator (ImmunoCard Operator I) safely manufactures FDA regulated medical devices in a fast-paced and results-oriented environment, meeting quality standards in accordance with cost, schedule and all standard cGMP operating procedures and guidelines.
Company
Meridian Bioscience, Inc.
Job Locations US-TN-Memphis
A Production Technician II, is responsible for performing tasks related to the production and purification of virus in a manufacturing facility. Specific duties include viral infection, harvesting, and purification as well as completion of corresponding documentation in compliance with internal SOPs and applicable regulatory requirements. The Production Technician II is also responsible for performing duties required in the implementation and continued improvement of the current manufacturing process.
Company
Meridian Life Science, Inc.
Job Locations US-OH-Cincinnati
The Vice President, Information Technology (VP, IT) serves as a member of the Executive Leadership Team and is responsible for leading all aspects of Meridian’s global Information Technology (IT) functions and infrastructure.  Ensures continuous delivery of IT services through oversight of service level agreements with end users and monitoring of IT systems performance. Ensures IT system operation adheres to applicable laws and regulations. Establishes lines of control for current and proposed information systems. Responsible for Global IT security, International accreditation infrastructure risk management and global IAO compliance management and government functions.
Company
Meridian Bioscience, Inc.
Job Locations US-TN-Memphis
The Sales Systems & CRM Administrator will develop and engineer key software elements to support the LIFE SCIENCE project goals as part of the implementation of CRM. Responsibilities included but not limited to: creating and developing solutions at every level of the software from the user interface, business logic, and CRM scripts and processes. The successful candidate will maximize Meridian’s LIFE SCIENCE market share and sales opportunities by making complete utilization of CRM database development, analytics and maintenance.
Company
Meridian Life Science, Inc.
Job Locations US-MA-North Billerica
Responsible for supporting post market regulatory activities regarding complaint analysis, MDR submissions, post market risk assessments (HHA), supports maintenance of the product Technical File in support of CE Marking, and risk management file updates. Also leads field safety corrective actions/recalls, as required. He/she 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.
Company
Meridian Bioscience, Inc.
Job Locations US-Remote
The Business Development Manager will achieve financial plan for territory or accounts assigned for the Life Science unit.  This person will be responsible for positioning and selling Meridian Bioscience’s portfolio of molecular biology regents, antigens and antibodies, and services to commercial partners.  To accomplish these goals, the successful candidate will utilize effective territory and account management strategies and utilize his/her technical background in a consultative selling manner in order to drive revenue growth with companies developing and building tests and assays in the human diagnostic, animal diagnostic and environmental testing markets. The successful candidate will maximize Meridian’s Life Science market share in existing and new accounts and sales opportunities by promoting product growth and providing development, management and account direction for assigned territory.
Company
Meridian Life Science, Inc.
Job Locations US-MA-North Billerica
The role of the Post Market Vigilance (PMV) Specialist encompasses the responsibilities described below and builds in additional functions, based on experience and proven aptitude. The PMV Specialist is to be an expert in the functioning and application of Magellan Diagnostics' products. This knowledge will be used to support all postmarket compliance activities including customer complaint handling, Medical Device Reports (MDR) / Vigilance Reports (MDV),  and to participate in the team that provides technical product support as well as product training to internal and external customers, as needed. Users including nurses, doctors, and laboratory technicians as well as sales, marketing and other personnel.
Company
Magellan Diagnostics Inc.