Artivion Inc. is seeking a highly motivated tax professional to join our tax accounting and reporting team at our fast growing, multinational public company. The tax manager will work closely with the tax director to provide tax provision, compliance, and planning support as well as process improvements to scale tax operations. This opportunity requires strong analytical,

To assist with management and control of all Artivion documents maintained in the Documentation System and administrative functions of the eQMS module. Ensure compliance to all internal procedures and external regulatory requirements. To ensure that all areas outlined under "Principal Responsibilities" are accomplished in an efficient, professional manner to support Artiv

The Aseptic Packaging Technician will support the TPL and company through performance of aseptic processing, packaging and labeling of allografts, and general lab functions. To learn more about Artivion's allograft products, Responsibilities Package and cryopreservation of cardiovascular allografts. Document vascular allograft attributes. Handle cryopreserved allografts.

The Global Stock Plan Administrator will manage the end to end administration of our equity plan. This role administers the company stock plans, prepares and provides information to stock plan participants, manages the processing of grants, award terminations, equity vesting, exercises, share pool tracking, and the employee stock purchase plan. The position will maintain

The Lab Technician will support the Tissue Processing Lab and Artivion through performance of aseptic processing of allografts and general lab functions. To learn more about allografts Responsibilities Sterile and non sterile duties for aseptic transfers. Receiving, inspection, labeling and documentation of incoming tissue. Circulate at dissection. Disinfect, assemble, an

The Senior SQL Database Administrator is responsible for Enterprise Database Management for Artivion, Inc., globally. This position will provide senior level capabilities relative to database solutions and sizing for the company, leads and drive database projects and is responsible for the daily operations and performance of the SQL Database Environments within Artivion,

Perform/lead Tier I Manufacturing tasks and become proficient in Tier II and III. GMP (Good Manufacturing Practices). Maintain individual training for all manufacturing tasks; ensure training compliance and strict adherence to SOPs (Standard Operating Procedures) Follow all Safety protocols and procedures in accordance with OSHA and corporate guidelines Perform all proces

A Final Assembly Technician I performs work station assembly operations including sewing and packaging of heart valves in a clean room. This person also inspects incomplete and finished components for conformance to written specification with the aid of a microscope, follows standard work methods, and practices safe work habits to ensure production is as efficient and saf

Perform/lead Tier I Manufacturing tasks and become proficient in Tier II and III. GMP (Good Manufacturing Practices). Maintain individual training for all manufacturing tasks; ensure training compliance and strict adherence to SOPs (Standard Operating Procedures) Follow all Safety protocols and procedures in accordance with OSHA and corporate guidelines Perform all proces

A Component Processing Technician in Subassembly inspects, tests, and assembles heart valves. This person also cleans and packages heart valves and OEM components and visually and dimensionally inspects components for conformance to written specification with the unaided eye and the aid of a microscope. Principal Responsibilities Visually inspect components with the aid o

Support product line compliance to US and International regulations and standards as applicable Writing clinical regulatory documents including annual reports, study summaries, and other study rationales. Support clinical requirements for regulatory submissions and maintenance. Coordinating company deliverables such as but not limited to the CEP, CER, PMCF activities and

Responsible for operating the Quality Management System (QMS). To assist in providing assurance the Company operates in compliance with all required regulations and standards as determined by both internal and external assessments. Lead internal audits and help manage external assessments. Provide training and champion the Quality Management System. To assure the Correcti

The Lead CRA will provide oversight, leadership, and guidance in the management and execution of clinical trial monitoring and to ensure compliance and quality. May also be responsible for leading their assigned CRAs on a study and timely study deliverables with quality and efficiency. Responsibilities Coordinate & manage clinical monitoring activities from site start up