Johnson & Johnson MedTech · 1 day ago
Senior Manager, Product Artwork Automation
Titusville, NJ
Full-time
Onsite
Senior Level, Lead/Staff
$122K/yr - $208K/yr
10+ years expJohnson & Johnson MedTech is dedicated to healthcare innovation, aiming to improve patient outcomes through advanced treatments. This role seeks a Senior Manager for Product Artwork Automation to lead technical initiatives and automation processes, ensuring compliance and operational efficiency while collaborating with cross-functional teams.
Hospital & Health Care
Responsibilities
Serve as the primary contact point & leader for all technical aspects of Product Artwork, providing strategic guidance and operational support for all our stakeholders & Business Partners
Accountable for supporting & troubleshooting all Product Artwork technical issues
Drive automation initiatives within the artwork management system (ArcTiC / Esko), partnering with Product Artwork and cross-functional teams
Ensure timely and compliant delivery of Product Artwork Automation that meets all HA and company standards
Leverage innovative technology, best practices and synergies for operational / automation efficiency in compliance with J&J Policy and local HA Requirements
Establish and lead cross-functional automated artwork template governance to drive and maintain standardization, ensuring robust control over automated artwork template design and usage
Assess and manage the impact of change requests to safeguard compliance, minimize risk, and sustain template efficiency
Responsible for the design, review, and enhance Product Artwork technical and automation processes; establish KPIs to monitor performance and value creation
Work closely with stakeholders to include IT, Regulatory, Quality, Packaging Sites, Brand Protection, Supply Chain, and external partners / vendors to drive seamless automation integration; and deliver proactive, expert technical support for all artwork-related processes
Build and maintain a high-performing, inclusive team culture; coach and develop talent while fostering a our Credo-based environment
Ensure adherence to artwork systems and regulatory standards; proactively identify and mitigate technical and automation risks
Work with PA LT to manage departmental budgets, optimize resource allocation, and manage workload effectively
Benchmark best practices, strengthen internal capabilities, and leverage external partnerships for non-core activities
Continuously report progress, challenges, and achievements to senior leadership and stakeholders
Qualification
Required
Bachelor's degree required; MBA or advanced degree in Engineering, Business, or Supply Chain preferred
A minimum of 10 years of relevant experience in a Pharmaceutical / regulated environment
Technical & automation related experience in artwork or packaging fields
Experience in coordinating / troubleshooting artwork, Regulatory Labeling & packaging design
4 years' people management experience in a diverse and multicultural environment, coaching and developing employees, communicating a clear vision and strategy, and leading a team through a change management journey
At least 4 years' exposure to and general understanding of regulatory processes and systems and/or in pharmaceutical packaging, artwork management, or related fields
Strong understanding of regulatory requirements pertaining to artwork, packaging, and labeling in the pharmaceutical industry
Supply Chain experience, including expertise in value chain, packaging sites, MSAT, external vendor management, and/or related areas
Knowledge of artwork and printed packaging materials and interfaces with key functions
High intellectual curiosity to challenge the status quo and learn artwork processes and how they relate to other supply chain processes as well as impact on the customer experience
Strong interpersonal skills, team player, influencing without authority, setting priorities and strong demonstrated stakeholder management
Experience with guides and regulations as well as industry technical standards related to artwork, including experience with international and pharmaceutical regulatory authorities. Knowledge & expertise in applying cGMP regulations (e.g., FDA, GMP, ICH, etc.)
Excellent organizational skills; in organizing/prioritizing work/projects, managing resources and budgets
The ability to multi-task, work with minimal supervision, and demonstrate resiliency and high productivity with constraints of schedule and budget
Strong cross-functional business acumen with a comprehensive understanding of end-to-end supply chain processes
Excellent interpersonal and communication skills, capable of influencing without authority, at all levels of the organization, and managing partner relationships effectively with various stakeholders
Proficient in tracking process improvements and measuring business value realization
Preferred
Life Sciences or Pharmaceutical industry experience
Lean/Six Sigma certification
Familiarity with artwork systems (e.g., ArcTiC / Esko)
Experience in setting up KPIs and managing departmental budgets
Experience in familiarity with design software tools (e.g. InDesign, Illustrator)
Benefits
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member
Caregiver Leave – 10 days
Volunteer Leave – 4 days
Military Spouse Time-Off – 80 hours
Company
Johnson & Johnson MedTech
At Johnson & Johnson MedTech, we are working to solve the world’s most pressing healthcare challenges through innovations at the intersection of biology and technology.
10001+ employees
Funding
Current Stage
Late StageLeadership Team
Mike Walker
CFO & VP of Finance DePuy Synthes
Tino Schweighoefer, MBA
CFO Monarch Platform
Company data provided by crunchbase