Labeling Specialist
Listed on 2026-07-16
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
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's four major groups of products include aortic stent grafts, surgical sealants, On‑X mechanical heart valves, and implantable cardiac and vascular human tissues. 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,
This position is responsible for coordinating, updating and maintaining accurate product labeling to support operational, regulatory, and quality requirements. This role works closely with Operations, Quality, Regulatory, Marketing, and Supply Chain teams to ensure labels are created, approved, and updated in production systems.
Responsibilities- Prepare and coordinate the creation, review, approval, release, and implementation of product labels
- Ensure labels comply with internal standards and applicable regulatory requirements
- Coordinate obtaining translations and proofs from outside vendors
- Become proficient with labeling software, templates, and version control systems
- Support production schedules by ensuring correct labels are available when needed
- Become proficient with label printers and LVS systems to assist with minor problems
- Prepare and coordinate label changes due to regulatory updates, product changes, or process improvements, including any associated document changes required as part of label updates.
- Perform quality checks to verify label accuracy, formatting, and revision control
- Collaborate with cross‑functional teams (Operations, Quality, Regulatory, Engineering)
- Document labeling processes and support audits or inspections
- Investigate and resolve labeling errors or discrepancies. Proactively identify opportunities to eliminate labeling errors.
- Identify gaps and perceived operational issues and prepare proposals on areas for improvement.
- Works independently to moderately complex labeling changes
- Bachelor's degree in Operations, Supply Chain, Life Sciences, or a related field
- 2‑5 years of experience in labeling, operations, manufacturing, or supply chain coordination
- Experience in regulated environments (e.g., pharmaceuticals, medical devices, food) is a plus
- Strong attention to detail and organizational skills
- Ability to manage multiple tasks and deadlines
- Familiarity with labeling systems, document control, or ERP systems
- Strong written and verbal communication skills
- Problem‑solving and root‑cause analysis skills
- Proficiency in Microsoft Office (Excel, Word)
- Ability to work independently and collaboratively
- Knowledge of regulatory labeling requirements
- Experience with change control or quality management systems
- Continuous improvement mindset
This is a hybrid position that will report to our Kennesaw, GA location 3 days per week.
Equal Opportunity EmployerThis 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.
#J-18808-Ljbffr(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).