MicroVention is now Terumo Neuro
Terumo

Labeling Lead

Position Overview

Support project teams in developing, finalizing, and implementing product labels, instructions for use, and patient implant cards. Ensure labels adhere to regional requirements, international standards, and cross-functional input from Marketing, R&D, Regulatory Affairs, and Legal. Job duties:
  • Support labeling activities for multiple projects from initiation to product launch.
  • Work alongside cross-functional project teams to develop labels that meet the needs of customers and all regional regulatory requirements.
  • Execute label development schedule, ensuring timely delivery of draft labels for submissions and release of finished labels into production.
  • Ensure all labeling changes comply with company policies and procedures.
  • Collaborate with Labeling Design team to ensure labeling requests are completed accurately and promptly.
  • Update project tracker and proactively communicate any delays or scope changes to proper stakeholders.
  • Ensure appropriate testing is performed prior to implementation of pre-production printing (e.g., legibility, bar code scanning, content accuracy, language, etc.).
  • Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
  • Perform additional duties as assigned.

Job Details

Job ID 12535BR

Aliso Viejo, California, USA

Salary Range:

$69,145 - $96,802

    1. Associate degree or equivalent combination of education and experience.
    2. Minimum three (3) years of relevant experience in product labeling in medical device field.
    3. Ability to design and modify labels, IFUs, and Patient Implant Cards.
    4. Working knowledge of relevant labeling standards (e.g., 21 CFR 801 – Labeling, 21 CFR 820 – Device Labeling, 21 CFR 830 – Unique Device Identification, FDA 89-4203, ISO 15223, CDRH Guidance Document, etc.).
    5. Excellent written and verbal communication skills.
    6. Proficient with MS Office applications, including Word, Excel, Outlook, and Teams.
    Desired Qualifications
    1. Basic knowledge of global regulations and guidelines pertaining to labeling.
    2. Demonstrated ability to understand the implications of label changes on pending and approved labels.
    3. Ability to present labeling design and implementation strategies and obtain alignment from stakeholders.
    4. Ability to translate regulation requirements into practical procedures accurately.
    5. Demonstrated skills in project management.
    6. Experience successfully managing projects with the ability to motivate cross-functional teams to complete their assigned tasks.
    7. Skills in cross-functional decision making.
    8. Ability to work effectively and confidently in a team environment.
    9. Ability to multi-task and prioritize projects to meet deadlines.
    10. Bachelor’s degree in a relevant field of study.
    11. Minimum one (1) year of experience in project management.
    12. Minimum five (5) years of relevant experience in product labeling in medical device field.