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The Laboratory Animal Assistant is an entry level position for candidates seeking an opportunity within animal
laboratory science or the biotech industry. The position is responsible for performing assigned animal husbandry,
colony management, ascites manufacturing and laboratory support activities according to company policies,
SOPs, and quality regulations. The position will provide support for the manufacturing of our antibody products
within a regulated environment.
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 of Care Specialist (RPOC) position within 18-24 months of being in the Inside Sales role. Field sales opportunities may be located anywhere in the US and will require relocation within the assigned territory.
The Clinical Support Coordinator is responsible for coordinating and managing the logistics and supply chain activities associated with clinical trials while adhering to regulatory requirements. This includes planning, forecasting, procurement, distribution, and tracking of biospecimens and supplies to ensure they reach clinical trial sites in a timely and compliant manner.
The CSC is also responsible for providing administrative and logistical support to the clinical trial team, ensuring the smooth and efficient conduct of clinical trials. This role involves collaboration with various stakeholders, including suppliers, regulatory authorities, clinical operations team members and collaborators from other departments.
Reporting to our SVP and General Counsel, this position will provide day-to-day global support for Meridian’s non-FDA compliance and CSR programs including, but not limited to, trade compliance, anti-corruption compliance, competition/antitrust compliance, conflicts of interest, gifts and entertainment, Code of Ethics, GDPR/Privacy law, Government Contracting, Conflict Minerals compliance, CSR (Corporate Social Responsibility), etc.
This position will be responsible for achieving financial plan for territory or accounts assigned for the Life Science unit by effectively managing territory and account strategy implementation with key accounts, consultative selling, and providing technical assistance for new & existing customers in the field of molecular and immunological testing; maximizing 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.
This position will be responsible for achieving financial plan for territory or accounts assigned for the Life Science unit by effectively managing territory and account strategy implementation with key accounts, consultative selling, and providing technical assistance for new & existing customers in the field of molecular and immunological testing; maximizing 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.
The Clinical Research Associate is responsible for the identification, qualification, management and monitoring of clinical study sites and reference laboratories to support Meridian Bioscience clinical development programs. Provide input on the development of the protocols, create the monitoring plan and other study material. Coordinate and oversee the execution of clinical evaluations and trials. Participate in departmental projects within Blood Chemistry, Immunology and/or Molecular at different phases, varying in scale and complexity.
A Facility Support Specialist will support daily services for the Physical Plant Department. The Specialist will help in establishing procedures and standards to improve efficiency and effectiveness of operations. The Specialist will rely on experience and judgment to plan and accomplish projects and goals.
Responsible for coordination and task execution for labeling of FDA regulated products and associated activities. Position works in collaboration with Regulatory Affairs, Marketing Communications, Document Control, and other departments as needed. Performs all tasks in compliance with the company’s Quality System requirements.
The position performs functions within the marketing department that:
- Provide guidance and direction to the training and development of the commercial teams globally.
- Training participants will be assessed on their competency on content, demonstration of retention of content, application of skills and demonstrated success on the job. This process of demonstrating competency will be referred to as certification. Certification shall be measured and compared to completion of quarterly and annual commercial goals.
- Provide oversight to development, delivery, measures of success, and curriculum completion for all components of commercial training and development.
- Stay abreast of industry training and development trends, provide continuous focus on strategies that support achievement of evolving commercial priorities.
- The position requires the necessary leadership skills that will help lead Meridian Diagnostic team to meet and exceed the company’s goals in the area of sales and profits.
Le technicien contrôle qualité exécute les contrôles qualités nécessaires à la relâche des produits. Il procède aux manipulations et expériences dans un environnement hautement réglementé pour des produits destinés à la vente et répondant aux exigences des autorités réglementaires.
Relevant du Gestionnaire, assurance qualité et contrôle qualité, le spécialiste assurance qualité travaille au suivi du système qualité selon les procédures établies à l’interne. Il assure le respect des processus du département qualité selon les exigences mises en place.
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. Medical, Dental and Vision offered day 1! Excellent paid time off.
Responsible for maintaining a timely flow of incoming raw materials, as well as the inspection of quality finished product for release to inventory. A heavy emphasis on documentation and process controls in compliance with current Quality System Regulations and ISO standards is required.
The Laboratory Animal Assistant is an entry level position for candidates seeking an opportunity within animal
laboratory science or the biotech industry. The position is responsible for performing assigned animal husbandry,
colony management, ascites manufacturing and laboratory support activities according to company policies,
SOPs, and quality regulations. The position will provide support for the manufacturing of our antibody products
within a regulated environment.
The Laboratory Animal Assistant is an entry level position for candidates seeking an opportunity within animal
laboratory science or the biotech industry. The position is responsible for performing assigned animal husbandry,
colony management, ascites manufacturing and laboratory support activities according to company policies,
SOPs, and quality regulations. The position will provide support for the manufacturing of our antibody products
within a regulated environment.
The Production Technician has primary responsibility for production of in-vitro medical diagnostic products in accordance with current manufacturing directions, SOPs, GMPs, and QSR to meet or exceed quality specifications on schedule at or below standard costs. Identify areas, formulate and execute plans for manufacturing process quality and efficiency improvements. Work in collaboration with Manufacturing, Quality Systems, Technical Support, Sales and Marketing to ensure product quality and availability.
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. Medical, Dental and Vision offered day 1! Excellent paid time off.
The Molecular Operator has primary responsibility for dispensing of in-vitro medical diagnostic reagents in accordance with current manufacturing directions, SOPs, GMPs, and QSR to meet or exceed quality specifications on schedule at or below standard costs.
This position requires someone to be Tobacco free.
The Shipping Clerk I position is responsible for all outbound shipments including picking, packing and processing, as well as verifying and maintaining records on outgoing shipments.