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, www.artivion.com.
Position Overview:
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
Qualifications:
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.
Our purpose is to develop simple, elegant solutions that address cardiac and vascular surgeons’ most difficult challenges in treating patients with diseases of the aorta and to deliver breakthrough technologies of unsurpassed quality that have far-reaching impact.
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