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ClinChoice

Labeling Artwork Controller Consultant

ClinChoice

. Manage the end-to-end artwork development process from initiation through approval and release .

Posted 11/4/2026contractRemote • CzechiaSeniorLeadWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing the end-to-end artwork development process, ensuring compliance with global regulatory requirements while leading cross-functional teams. Proficient in utilizing digital tools and systems for project management and artwork validation.

Highest-signal resume keywords
Artwork Development ManagementRegulatory Compliance KnowledgeProject Management ExpertiseAdobe Creative Suite ProficiencySix Sigma Green Belt Certification

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Labeling DesignProofreadingResource PlanningProcess ImprovementColor ManagementRegulatory Content ValidationProject TrackingArtwork Issue ManagementFeasibility ConsultationCross-Functional Coordination
Soft Skills
Excellent CommunicationProblem-SolvingOrganizational Skills
Tools & Technologies
PLM SystemsAgileGLAMSLoftwareVeracitiVeevaAdobe IllustratorAdobe InDesignAdobe PhotoshopAdobe Acrobat Pro
Certifications & Qualifications
Six Sigma Green Belt CertificationPMP Certification
Industry Keywords
Consumer HealthPharmaceuticalMedical DeviceGlobal Regulatory RequirementsPackaging TechnologyArtwork ControllersPre-Press ProcessesPrint ProcessesColor Management AssessmentsCorrective and Preventive Actions

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Manage the end-to-end artwork development process from initiation through approval and release
  • Coordinate PMO, Regulatory Affairs, Marketing, Packaging, Quality, Supply Chain, and external vendors/agencies
  • Validate briefs and resolve discrepancies with cross-functional teams
  • Oversee timelines, resource planning, and progress tracking for concurrent labeling projects
  • Coordinate review and approval of labeling content and artwork for regulatory, legal, and corporate compliance
  • Drive process improvements for artwork development, approval workflows, and digital tools
  • Investigate Root Cause Analyses and implement Corrective and Preventive Actions
  • Maintain artwork issue logs and attend escalation meetings
  • Manage Veraciti system issues and escalate appropriately
  • Create and maintain training documentation; onboard new hires and conduct quarterly refreshers
  • Supervise Artwork Controllers and support SMEs, Process Leads, vendors, and Hub Leads
  • Track action items and communicate project status, risks, and milestones
  • Attend regional project meetings and contribute to dashboards, analytics, KPI reviews, and compliance initiatives
  • Gather requirements for regional jobs, assess resources, and provide quotations
  • Conduct design-to-press color management assessments and feasibility consultations
  • Monitor regional project timelines and costs, resolve roadblocks, and address executional quality issues
  • Manage ad-hoc artwork requests and cascade process/system communications

Requirements

What you’ll need
  • 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
  • PMP certification or formal project management training is a plus

Benefits

Comp & perks
  • 12 months contract with possibility of extension
  • Remote option
  • Career opportunities working for a global CRO
  • Continuous training and professional development
  • Equal opportunity and diversity/inclusivity environment