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Manager, Commercial Artwork Development

BeiGene

Any City, USRemotePosted 1 day ago$123,100.00 - $163,100.00 annually
Full TimeSenior LevelOperations & Supply ChainBiotechnology
Original posting ↗

Summary

The Manager, Commercial Artwork is responsible for development, approval, and control of commercial labeling artwork requirements supporting finished goods packaging for BeOne Commercial Products.

Job description

Responsibilities

  • Collaborate with contract artwork vendors, contract manufacturing partners, commercial label printers, and key stakeholders/cross-functional project teams to gather market-specific information for label development.
  • Deliver flawless artwork design and coordination per agreed timelines.
  • Contribute to labeling development efficiencies through standard processes and platforms to enhance commercialization and lifecycle management globally.
  • Initiate and track progression of labeling artwork projects to ensure artwork deliverable commitments for Health Authority submissions, commercial product launches, test component artwork, and labeling artwork lifecycle updates.
  • Accountable for market-specific artwork layout of product package insert, carton and container labeling, including printer proof approvals when applicable.
  • Support end-to-end commercial artwork process improvements including artwork creation, version control, content verification, cross-functional stakeholder review and approvals, production implementation, and commercial artwork repository.
  • Facilitate initiation, progression, and closure of commercial artwork designated change controls, including impact assessments, change actions, and other commercial artwork specific QMS document records.
  • Align with key stakeholders for increased efficiency in commercial artwork process and documents through Global Standards and local SOPs.
  • Identify complexities/process gaps and proactively contribute to effective solutions.
  • Represent and participate in cross-functional project teams to align on project goals, establish timelines, and track artwork progression to completion.
  • Effectively manage artwork development, version control, and approvals to provide deliverables supporting HA submissions, market launches, new indication implementation, and product labeling lifecycle updates.
  • Focus on right first time, lead time, and other metrics to measure performance.
  • Ensure area of responsibility complies with appropriate change control and current quality systems and company policies.
  • Work with designated consultants, contract manufacturers, and external business partners to ensure compliance with business standards and requirements.

Qualifications

  • 5+ years progressive experience in Artwork development and control preferably within the biotech, medical device, pharmaceutical industry or related industry.
  • Experience with leading strategic initiatives in the pharmaceutical, biotech or related industry is highly preferred.
  • Bachelor Degree in Graphic Design, Package Engineering, Supply Chain, Life Sciences or similar education required.
  • Commensurate combination of education and relevant experience in pharmaceutical artwork management or supply chain functional areas may also be considered.
  • Experience working in a global, complex supply chain organization preferred.
  • An innovative mindset, with an ability to embrace change, respect differences of opinion, communicate openly and build consensus.
  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint), MS Teams, Sharepoint.
  • Experience in Veeva, Artwork Management System, Adobe Illustrator, and InDesign are beneficial but not required.
  • Travel up to 20%.

Requirements

  • 5+ years progressive experience in Artwork development and control
  • Experience preferably within biotech, medical device, or pharmaceutical industry
  • Bachelor Degree in Graphic Design, Package Engineering, Supply Chain, Life Sciences or similar education required
  • Commensurate combination of education and relevant experience may be considered
  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint), MS Teams, Sharepoint
  • Experience in Veeva, Artwork Management System, Adobe Illustrator, and InDesign beneficial but not required
  • Experience working in a global, complex supply chain organization preferred
  • Experience with leading strategic initiatives in pharmaceutical, biotech or related industry highly preferred
  • Travel up to 20%

Benefits

  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness Program
  • Equity Awards
  • Employee Stock Purchase Plan
  • Annual Bonus Plan

Company overview

BeiGene, Ltd., now rebranding as BeOne Medicines, is a global commercial-stage biotechnology company specializing in the discovery, development, manufacturing, and commercialization of innovative oncology medicines. Founded in 2010 by John V. Oyler and Xiaodong Wang, the company has grown into a multinational organization with headquarters in Cambridge, Massachusetts, Beijing, China, and Basel, Switzerland. BeiGene focuses on developing targeted and immune-oncology therapies for cancer treatment, with a diverse pipeline that includes internally discovered products like BRUKINSA (zanubrutinib), a Bruton's tyrosine kinase inhibitor, and Tevimbra (tislelizumab), a PD-1 inhibitor. The company operates across six continents with over 45 countries participating in clinical trials and has enrolled more than 30,000 patients in its research programs. With approximately 12,000 employees worldwide, BeiGene has established itself as a significant player in global oncology, particularly with strong market presence in China and expanding operations in the United States and Europe. The company's mission centers on expanding access to high-quality cancer therapies worldwide through persistent innovation and challenging traditional approaches to drug development.

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