לוח אפשרויות קריירה - הדרך החכמה להייטק

The opportunity
 
This is a mid-level position responsible for prioritizing and managing labeling artwork development within the Artwork Management Team for new and revised packaging components. Concurrently manage multiple projects to ensure artwork is available to meet FDA submission dates as well as production dates with minimal supervision. 
 How you’ll spend your day
 
– Independently or with minimal supervision, prioritize and manage labeling projects and the development of labeling artwork through the Graphic Artist, Proofreading and Package Engineering groups within Teva Operations. –    Responsible for the initiation of project binder routing for new or revised labeling artwork files through the Packaging sites, Marketing, Regulatory groups and/or affiliates. –    Leverage detailed knowledge of complex pharmaceutical labeling artwork production requirements to assess labeling requests to ensure that all relevant information required to develop artwork is included; (Regulatory drafts, labeling colors, trade dress, technical drawings, bar codes, item codes, and country requirements, Etc.)-    Assess incoming artwork development requests to identify critical path tasks and proactively initiate an appropriate strategy to ensure efficient and compliant implementation. –    Actively collaborates with internal and external customers to obtain any additional documentation required to enable the artwork development process.  Resolve issues when appropriate with internal/external customers.  –    Responsible for reviewing change control for accuracy, completeness, compliance and appropriateness of supporting documentation. –    Prepare project binders with supporting documentation and instructions. Execute the necessary forms required to develop artwork right the first time. –     Act as a liaison between the stakeholders, manufacturing sites, and corporate departments to compile all relevant information needed to accurately develop, review, and approve labeling artwork.-    Responsible for assignment, and logging of all codes where applicable (bar codes, human readable characters, components number, and revision number) to the requested labeling.  –    Initiate artwork in Veeva software application for each new/revised labeling component.-    Attend Project Management meetings as a subject matter expert to facilitate the artwork process development.   Communicate labeling artwork development requirements and gather project timelines and communicate expectations to appropriate stakeholders.-    Responsible for compliance with current appropriate Federal Regulations and guidelines on artwork and labeling, Teva labeling format, and relevant SOP’s.