商業標籤項目經理（完全遠程）
Commercial Labeling Project Manager (Fully Remote)
这是一个远程职位。
我们的客户是生物技术和生命科学领域的全球领导者，现正在寻找一名“标签项目经理（全职远程）”。
薪资：55-61美元/小时（W2，根据经验而定）
工作时长：长期合同（可能延长）
公司福利：医疗、牙科、视力、带薪病假、401K
简介：在此职位中，您将负责管理端到端的标签流程，协调艺术作品更新，跟踪项目时间表，并在受监管的制药环境中确保标签变更的合规执行。理想的候选人应具备商业标签、法规运营、艺术作品管理和包装运营方面的经验，以及使用Veeva Vault或类似文档管理系统的工作经验。
关键职责
· 从启动到最终审批，管理端到端的商业标签项目。
- 协调艺术作品评审周期、校对修订和最终审批，与跨职能团队合作。
- 使用Veeva Vault或类似系统进行标签流程的路由和管理。
- 与法规、质量、供应链、包装、制造和外部印刷供应商合作。
- 审核艺术作品样稿，并使用Adobe Acrobat和GlobalVision（或类似工具）进行详细校对。
- 跟踪多个项目的项目时间表、里程碑、交付物和审批状态。
- 支持标签变更的实施，包括逐步替换/退出活动和过时库存跟踪。
- 所需资格
- 在制药或生物技术标签、法规运营、包装或供应链领域有3-5年以上经验。
- 具有管理商业标签流程和艺术作品评审过程的经验。
- 具有Veeva Vault或类似文档管理/工作流系统的实际操作经验。
- 具有使用Adobe Acrobat进行文档审核和校对的经验。
- 具有强大的项目协调和组织能力。
- 优先资格
- 在GxP监管的制药或生物技术环境中工作的经验。
- 了解全球商业标签流程。
- 具有与全球利益相关者协调的经验。
- 如感兴趣，请将更新的简历发送至 /。
- 最初发布于Himalayas
查看英文原文
This is a remote position.
Our client, a world leader in biotechnology and life sciences, is looking for a “Labeling Project Manager (Fully Remote)”.
Rate:$55-$61/hr on W2 (DOE)
Job Duration:Long-Term Contract (Possibility Of Extension)
Company Benefits: Medical, Dental, Vision, Paid Sick Leave, 401KSummary:In this role, you will be responsible for managing end-to-end labeling workflows, coordinating artwork updates, tracking project timelines, and ensuring compliant execution of labeling changes in a regulated pharmaceutical environment. The ideal candidate has experience in commercial labeling, regulatory operations, artwork management, or packaging operations, along with hands-on experience using Veeva Vault or similar document management systems.Key Responsibilities
· Manage end-to-end commercial labeling projects from initiation through final approval.
- Coordinate artwork review cycles, proof revisions, and final approvals with cross-functional teams.
- Route and manage labeling workflows using Veeva Vault or similar systems.
- Partner with Regulatory, Quality, Supply Chain, Packaging, Manufacturing, and external print vendors.
- Review artwork proofs and perform detailed proofreading using Adobe Acrobat and GlobalVision (or similar tools).
- Track project timelines, milestones, deliverables, and approval status across multiple projects.
- Support implementation of label changes, including phase-in/phase-out activities and obsolete inventory tracking.
Required Qualifications
· 3–5+ years of experience in pharmaceutical or biotechnology labeling, regulatory operations, packaging, or supply chain.
- Experience managing commercial labeling workflows and artwork review processes.
- Hands-on experience with Veeva Vault or similar document management/workflow systems.
- Experience using Adobe Acrobat for document review and proofreading.
- Strong project coordination and organizational skills.
Preferred Qualifications
· Experience in GxP-regulated pharmaceutical or biotechnology environments.
- Knowledge of global commercial labeling processes.
- Experience coordinating with global stakeholders.
If interested, please share your updated resume at /.
Originally posted on Himalayas