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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
Posted 10 days ago
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
Posted 11 days ago
The Lab Technician will support the Tissue Processing Lab and Artivion through performance of aseptic processing of allografts and general lab functions. Responsibilities Sterile and non sterile duties for aseptic transfers. Receiving, inspection, labeling and documentation of incoming tissue. Circulate at dissection. Disinfect, assemble, and sterilize laboratory instrume
Posted 11 days ago
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
Posted 12 days ago
Artivion
- Kennesaw, GA
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
Posted 12 days ago
Artivion
- Kennesaw, GA
The DQA Tech will ensure all donor information received is properly handled in an efficient, timely, and professional manner. Ensure all records associated with donor/tissue products and processes are properly identified, controlled, and tracked within the Donor Quality Assurance (DQA) file room. Ensure review of external Recovery Partner forms are complete and attached.
Posted 12 days ago
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
Posted 12 days ago
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,
Posted 27 days ago
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
Posted 1 month ago
Artivion
- Austin, TX
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
Posted 1 month ago
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
Posted 1 month ago
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