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Labeling Artwork Controller Consultant

ClinChoice
Contract type
One-time
Work mode
Remote · Italy
Experience
Lead / principal · 10+ years

Job description

A 12-month contract consultant role managing the end-to-end artwork development process for packaging and labeling components within a region, working remotely for one of ClinChoice's consumer product clients. The role combines hands-on execution with supervision of Artwork Controllers.

At a glance

Employment
Contract
Work mode
Remote · Italy

What you'll do

  • 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/agencies.
  • Validate briefs for accuracy and completeness; 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 (RCAs) and implement Corrective and Preventive Actions (CAPA) as needed.
  • Maintain artwork issue logs and attend escalation meetings to provide updates.
  • Identify inefficiencies and escalate 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; conduct quarterly refreshers on best practices.
  • Provide guidance on escalation channels and support SMEs, 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 (Kick-off, Overview, Alignment, Technical with Printer) and provide updates.
  • Share project insights for dashboards and analytics; contribute to KPI reviews and compliance initiatives.
  • Gather requirements for new regional jobs and assess resources 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; anticipate and resolve roadblocks.
  • Address process and executional quality issues; support system and process improvements.
  • Manage ad-hoc artwork-related requests and cascade process/system communications.

What we're looking for

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

Nice to have

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

How to get hired

  1. 1Once you have submitted your CV, you will receive an acknowledgement that we received it.
  2. 2If you have the requirements we need, you will be invited for phone interview as the first step.

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About ClinChoice

Global full-service CRO

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

Mission

To contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices

Key facts

  • over 4,000 professionals
  • Contract Research Organization (CRO)
  • Over 28 years of proven high-quality delivery and results across all our services
  • Over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific
  • Below industry average turnover rates

What they value

  • Diversity and inclusivity
  • Continuous training
  • Close management and training as the core instrument to develop and maintain highly-qualified personnel