Sr Labeling & Packaging DeveloperLocationUS-BothellID2023-1156CategoryQuality Assurance/Regulatory AffairsPosition TypeFull-TimeWork ModelOnsiteCompany OverviewVerathon is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality products that endure over time and ensure clinical and economic utility. Two areas where Verathon has significantly impacted patient care, and become the market leader in each, are bladder volume measurement and airway management. The company's BladderScan portable ultrasound and GlideScope video laryngoscopy & bronchoscopy systems effectively address unmet needs for healthcare providers and meaningfully raise the standard of care for patients. Verathon, a subsidiary of Roper Technologies, is headquartered in Bothell, Washington, USA and has international subsidiaries in Canada, Europe and Asia Pacific. For more information, please visit www.verathon.com.OverviewVerathon is looking for a Senior Labeling & Packaging Developer to become the newest member of ourQA/RA Team located in Bothell, WA.The Senior Labeling & Packaging Developer is responsible for providing proactive cross-functionalleadership and influencing across projects for the development of new and changes to existing productlabeling components and packaging for global markets.ResponsibilitiesDrive design and delivery of label and packaging component artwork files to support initial submissions and post-approval labeling changes in a highly regulated environmentManage and maintain label contentPerform labeling requirements and standards assessments by identifying requirements from new and updated standardsDevelop project plans to bring labeling into compliance with the latest standards and company guidelines (branding, trademarks)Lead and partner with cross-functional team to track and drive labeling activities to completionCollaborate with third parties to arrive at optimal label and packaging solutions within strict standards and branding requirementsCollaborate with and facilitate review and approval processes with appropriate cross functional teams such as Regulatory Affairs, Product Management, R&D, Operations, Supply Chain, and external parties to develop new or update existing labeling component artworkTake on related labeling needs, such as: leading Adequacy Reviews of all customer-facing technical product labeling, assessing compliance to global labeling requirements and standardsAbility to work autonomously on labeling activities, including projects and business tasks, both planned and unplanned with accelerated timelinesAid the Technical Communications team across projectsQualificationsBachelor's Degree is required; Masters preferred2+ years of relevant medical device experience, including working within the medical device product lifecycle like development, commercialization, and operations2+ years of experience creating labeling and packaging for European (MDD and MDR), US FDA, and Unique Device Identifier (UDI) requirementsExpertise in technical programs, particularly with Adobe Creative Suite, Cloud programs, Microsoft Office programs, and Seagull Scientific BarTender2+ years of experience with GS1/GS1-128 (GTIN)2+ years of experience with thermal printers, barcode scanners, and barcode parsingExpertise liaising with third-party vendors and in-house regulatory, manufacturing, engineering, and supply chain teamsDetail-oriented with the ability to proofread and check documents for accuracy and inconsistenciesAbility to critically and efficiently review detailed information to support a labeling r