Senior Manager, Project Artwork Automation
Job in
04100, Latina, Lazio, Italy
Listed on 2025-12-28
Listing for:
Johnson & Johnson MedTech
Full Time
position Listed on 2025-12-28
Job specializations:
-
Management
Operations Manager, Program / Project Manager, Business Management, Data Science Manager
Job Description & How to Apply Below
Johnson & Johnson Med Tech – Senior Manager, Project Artwork Automation
Location:
Beerse, Antwerp, Belgium;
Breda, Netherlands;
Cork, Ireland;
Latina, Italy
About the Role
We are searching for the best talent for a Senior Manager, Product Artwork Technical & Automation to join our Digital Operations and Technical Services Operation. The selected candidate will work with existing Product Artwork SMEs / team members to lead all technical and automation initiatives, develop standards and processes, and collaborate with cross‑functional teams to deliver efficient, compliant, and scalable automation & technical solutions.
This is an exciting opportunity shape the future of artwork operations during a digital / automation transformation. The position leads and adapts to change, manages complexity and works collaboratively and builds alliances with relevant parts of the business, including Regulatory Affairs, Supply Chain functions and external business partners.
Key Responsibilities
Serve as the primary contact point & leader for all technical aspects of Product Artwork, providing strategic guidance and operational support for all stakeholders & business partners.
Drive automation initiatives within the artwork management system (ArcTiC / Esko), partnering with Product Artwork and cross‑functional teams to ensure timely and compliant delivery of automation that meets all HA and company standards.
Establish and lead cross‑functional automated artwork template governance to drive and maintain standardization, ensuring robust control over automated artwork template design and usage.
Design, review, and enhance Product Artwork technical and automation processes; establish KPIs to monitor performance and value creation.
Work closely with stakeholders (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 Credo‑based environment.
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.
Qualifications
Bachelor’s degree required; MBA or advanced degree in Engineering, Business, or Supply Chain preferred.
Minimum 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.
At least 4 years’ exposure to and general understanding of regulatory processes and systems related to 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 and 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.
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…
Position Requirements
10+ Years
work experience
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