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Labeling Specialist II

  • ... Posted on: Mar 30, 2026
  • ... Glaukos Corporation
  • ... San Clemente, California
  • ... Salary: Not Available
  • ... Full-time

Labeling Specialist II   

Job Title :

Labeling Specialist II

Job Type :

Full-time

Job Location :

San Clemente California United States

Remote :

No

Jobcon Logo Job Description :

GLAUKOS - LABELING SPECIALIST II (San Clemente, CA). The Labeling Specialist is responsible for creating, updating, and managing product labeling for medical device and pharmaceutical products with moderate independence. This role supports labeling development from initial artwork through final approval, ensuring compliance with regulatory standards and internal procedures. The Labeling Specialist II partners with Regulatory, Quality, R&D, Operations, and external vendors to ensure accurate, consistent, and audit‑ready labeling. This role requires strong attention to detail, familiarity with labeling systems, and the ability to manage multiple labeling projects simultaneously. What Will You Do Create, update, and maintain labeling content, artwork, and drawings following Glaukos procedures Prepare labeling deliverables, ensuring accuracy, consistency, and regulatory compliance Manage ECOs, DCC changes, and related workflows with limited oversight Coordinate with vendors for translations, graphics support, and printed label production Ensure correct application of symbols, regulatory marks, and product identifiers Maintain document control accuracy across systems (Oracle, Veeva, TrackWise) Support creation and maintenance of in‑house printed labels (e.g., NiceLabel) Provide cross‑functional guidance on labeling standards and formatting Troubleshoot labeling issues and elevate discrepancies as needed Ensure labeling documentation remains audit‑ready and compliant with quality system requirements Support process improvements and labeling standardization initiatives Perform other duties as assigned How Will You Get Here 2–5 years of experience in labeling, document control, regulatory, or a related medical device/pharma field Bachelor’s degree preferred Strong understanding of labeling processes, document control, and version management Ability to read and understand drawings, artwork files, and regulatory symbols Proficiency in Microsoft Office; exposure to labeling tools (NiceLabel, Adobe, etc.) preferred Strong written/verbal communication skills Ability to manage multiple projects with minimal supervision Attention to detail, accuracy, and documentation quality #J-18808-Ljbffr

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Jobcon Logo Position Details

Posted:

Mar 30, 2026

Reference Number:

14660_25861DF7060A20E80BDFE08A60B57419

Employment:

Full-time

Salary:

Not Available

City:

San Clemente

Job Origin:

APPCAST_CPC

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GLAUKOS - LABELING SPECIALIST II (San Clemente, CA). The Labeling Specialist is responsible for creating, updating, and managing product labeling for medical device and pharmaceutical products with moderate independence. This role supports labeling development from initial artwork through final approval, ensuring compliance with regulatory standards and internal procedures. The Labeling Specialist II partners with Regulatory, Quality, R&D, Operations, and external vendors to ensure accurate, consistent, and audit‑ready labeling. This role requires strong attention to detail, familiarity with labeling systems, and the ability to manage multiple labeling projects simultaneously. What Will You Do Create, update, and maintain labeling content, artwork, and drawings following Glaukos procedures Prepare labeling deliverables, ensuring accuracy, consistency, and regulatory compliance Manage ECOs, DCC changes, and related workflows with limited oversight Coordinate with vendors for translations, graphics support, and printed label production Ensure correct application of symbols, regulatory marks, and product identifiers Maintain document control accuracy across systems (Oracle, Veeva, TrackWise) Support creation and maintenance of in‑house printed labels (e.g., NiceLabel) Provide cross‑functional guidance on labeling standards and formatting Troubleshoot labeling issues and elevate discrepancies as needed Ensure labeling documentation remains audit‑ready and compliant with quality system requirements Support process improvements and labeling standardization initiatives Perform other duties as assigned How Will You Get Here 2–5 years of experience in labeling, document control, regulatory, or a related medical device/pharma field Bachelor’s degree preferred Strong understanding of labeling processes, document control, and version management Ability to read and understand drawings, artwork files, and regulatory symbols Proficiency in Microsoft Office; exposure to labeling tools (NiceLabel, Adobe, etc.) preferred Strong written/verbal communication skills Ability to manage multiple projects with minimal supervision Attention to detail, accuracy, and documentation quality #J-18808-Ljbffr

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