DQA Technician

CryoLife, Inc.; Kennesaw, Northern (GA, KY); Hybrid; USD 42,000 - 60,000; Full time

Job summary

Artivion, Inc. in Georgia is seeking a DQA Technician to ensure donor information is processed accurately and efficiently.

The role involves handling donor/tissue product records, reviewing Recovery Partner forms, and maintaining the DQA file room to support quality systems. Under minimal supervision, you will perform data entry for serology and culture, coordinate with Human Tissue Quality Assurance, and help drive documentation compliance, training, and process improvements.

Qualifications

• High School diploma or equivalent required.
• 1-2 years of relevant experience.
• Organized, detail-oriented, adaptable.
• Able to follow instructions and work with minimal supervision.
• Good typing and communication skills; familiar with general office procedures.
• Must be able to commute to Kennesaw weekly; hybrid after training.

Responsibilities

• Input donor data from Recovery Partners into donor records.
• Perform data entry for donor records, including serology and culture entries.
• Maintain DQA file room and organize donor/tissue product information.
• Collaborate with Human Tissue Quality Assurance to gather graft records.
• Scan Certificates of Assurance to support Customer Service.
• Review Recovery Partner forms submitted to DQA.
• Complete review of all Rejected charts and update donor chart status.
• Understand ISO, AATB, GTPs and Quality System Regulations relevant to operations.
• Provide input to management for new/revised documents.
• Mentor and assist DQA Technicians.

Job description

• Quality Assurance
• Full-Time
• Requisition #: DQATE002533

Description

Company Overview:

Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons’ most difficult challenges in treating patients with aortic diseases. Artivion has over 1,600 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, www.artivion.com .

Position Overview:

The DQA Technician 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. Perform initial review of incoming donors to assess for infectious disease testing needs, internal pathology services, and accurate demographic information. With minimal supervision, ensure all areas outlined under “Principal Responsibilities” are accomplished in an efficient, professional manner to support Artivion.

Responsibilities:

• Use multiple systems and programs to process donor information received from external Recovery Partners, other processors, and laboratories to be inputted into the appropriate donor record.
• Perform data entry tasks for donor records, including but not limited to serology and culture entry.
• Maintain DQA File room, including organizing donor/tissue product information, periodically archiving Complete / Rejected charts, and maintaining relevant databases.
• Build a working relationship with Human Tissue Quality Assurance to gather and organize graft records.
• Scan Certificates of Assurance to support Customer Service.
• Review Recovery Partner forms that are submitted to DQA.
• Complete review of all Rejected charts and update the donor chart status as appropriate.
• Develop systematic methods for completing work assignments to ensure timelines are met and personal job commitments are accomplished.
• Understand ISO requirements, AATB, GTPs, and the Quality System Regulations as they pertain to the entire operation, i.e., nonconformities, Good Documentation Practices, calibration, equipment maintenance, product storage and identification, etc.
• Provide input to management that facilitates the process for new, revised, and obsoleted documents (policies, procedures, forms, templates, etc.) as they pertain to the job.
• Provide mentoring and assistance to DQA Technicians.
• Ability to lead and present ideas that are motivating, by maintaining positive support, setting a positive example, and establishing an overall objective and creative atmosphere.
• Increase productivity and revenues by optimizing processes and workflows.
• Effectively complete “other” functions that may be assigned.

Qualifications:

• High School Diploma or equivalent.
• 1-2 years of relevant experience
• Organized, detail-oriented, and adaptable.
• Capable of following instructions and working without direct supervision.
• Good typing and communication skills, knowledge of general office procedures.
• Must be able to commute to Kennesaw office on a weekly basis. Position will be hybrid once training is complete.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.