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ClinChoice

Global CRO providing full-service clinical development

Labeling Artwork Controller Consultant

Project ManagementConfirmed live in the last 24 hours
Full-timeRemote in CzechiaNo salary listed

About the Job

Requirements

  • A bachelor's degree in Life Sciences, Business, Packaging Technology, or a related field is required.
  • At least 10 years of experience in labeling design, proofreading, coordination, regulatory, packaging, and project management within consumer health, pharmaceutical, or medical device industries is required.
  • Strong knowledge of global regulatory requirements for product labeling and packaging is required.
  • The ability to manage multiple projects and cross-functional teams in a deadline-driven environment is required.
  • Hands-on experience with product lifecycle management and electronic artwork systems such as Agile, GLAMS, Loftware, Veraciti, or Veeva is required.
  • Expertise in Adobe Creative Suite, including Illustrator, InDesign, Photoshop, and Acrobat Pro, is required.
  • Familiarity with pre-press and print processes, including CMYK, Pantone, dielines, and bleed, is required.
  • Experience with proofreading tools such as TVT, GlobalVision, or InformCC, and regulatory content validation, is required.
  • Six Sigma Green Belt certification or equivalent experience in continuous improvement is required.
  • Strong communication, problem-solving, and organizational skills are required.

Responsibilities

  • Manage the end-to-end artwork development process from initiation through approval and release, ensuring timely delivery of high-quality labeling components.
  • Act as the primary liaison between PMO, Regulatory Affairs, Marketing, Packaging, Quality, Supply Chain, and external vendors or agencies.
  • Validate briefs for accuracy and completeness and collaborate with cross-functional teams to resolve discrepancies.
  • Oversee timelines, resource planning, and progress tracking for multiple concurrent labeling projects.
  • Coordinate review and approval of labeling content and artwork in internal systems, ensuring compliance with regulatory, legal, and corporate standards.
  • Drive process improvements related to artwork development, approval workflows, and digital tools.
  • Investigate root cause analyses and implement corrective and preventive actions as needed.
  • Maintain artwork issue logs and attend escalation meetings to provide updates.
  • Identify inefficiencies and escalate them to Hub Leads when required.
  • Participate in content lock meetings to ensure stakeholder alignment.
  • Manage Veraciti system-related issues and escalate appropriately.
  • Suggest and implement technology solutions for artwork and labeling processes.
  • Create, update, and maintain training documentation for systems and processes.
  • Supervise Artwork Controllers to ensure task completion and provide support during peak periods.
  • Onboard new hires on artwork management systems and end-to-end processes, and conduct quarterly refreshers on best practices.
  • Provide guidance on escalation channels and support subject matter experts, Artwork Process Leads, vendors, and Hub Leads with artwork production deployment.
  • Track and follow up on action items from cross-functional meetings.
  • Communicate project status, risks, and milestones consistently to stakeholders.
  • Attend regional project meetings, including kick-off, overview, alignment, and technical meetings with printers, and provide updates.
  • Share project insights for dashboards and analytics, and contribute to key performance indicator reviews and compliance initiatives.
  • Gather requirements for new regional jobs, assess resource requirements, and provide job quotations when required.
  • Conduct design-to-press color management assessments and feasibility consultations.
  • Monitor and maintain regional project timelines and costs, and anticipate and resolve roadblocks.
  • Address process and executional quality issues and support system and process improvements.
  • Manage ad hoc artwork-related requests and cascade process and system communications.

Desired Qualifications

  • PMP certification or formal project management training is a plus.

About the Company

ClinChoice

Global CRO providing full-service clinical development

ClinChoice is a global contract research organization (CRO) that provides outsourced clinical development services across the full lifecycle for pharmaceutical, biotechnology, medical device, and consumer health customers. It delivers services such as clinical operations, project management, biostatistics, data management, regulatory affairs, medical affairs, and pharmacovigilance to support trials from early development through post-approval. The company differentiates itself with a large, global workforce—over 4,000 professionals in more than 30 countries—and growth through mergers and acquisitions, enabling multinational trial execution. Its goal is to help clients accelerate approvals and navigate complex regulatory environments by offering flexible project-based and FSP engagement models for end-to-end development and lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Whitemarsh Township, Pennsylvania
Founded
1995

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