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

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

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

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

To provide current college students the opportunity to gain hands on research and development experience in the corporate medical device setting. Interns will be paired with a current member of R&D and will provide engineering support in the phases of device prototyping, test method development, characterization, and design verification testing. Interns will also have the