Senior Manager, Project Artwork Automation

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at are searching for the best talent for a Senior Manager Product Artwork Technical & Automation to join our Digital Operations and Technical Services Operation to be based in Schaffhausen Switzerland.

About the Role

At Johnson & Johnson we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented treated and cured where treatments are smarter and less invasive and solutions are personal. Through ourexpertisein Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundlyimpacthealth for humanity. Learn more at you interested in joining a team that is positivelyimpactingand improving patients lives by ensuring high quality in the manufacturing of our products Apply today for this exciting opportunity!

The selectedcandidatewillwork with existing ProductArtworkSMEs/teammemberstolead all technical and automation initiatives develop standards and processes and collaborate with cross-functional teams to deliver efficient compliant and scalableautomation & technicalsolutions. This is an exciting opportunity to shape the future of artwork operations during a major digital/ position leads and adapts to change managescomplexityand works collaboratively and builds alliances with relevant parts of the business including Regulatory AffairsSupply Chain functionsand external business partners toleverageexpertise resourcesprocessesand tools.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings we recommend focusing on the specific country(s) that align with your preferred location(s)

United States & Puerto Rico-Requisition Number: R-050072

Belgium Ireland Italy & The Netherlands- Requisition Number: R-050839

Switzerland - Requisition Number: R-0500840

Remember whether you apply to one or all of these requisition numbers your applications will be considered as a single submission.

Key Responsibilities:

The successful candidate willserveas the primarycontact point& leaderfor all technical aspects of Product Artwork providing strategic guidance and operational supportfor all our stakeholders & Business for supporting & troubleshooting all Product Artwork technical issues.

They will drive automation initiatives within theartwork management system (ArcTiC / Esko)partnering with ProductArtworkand cross-functional compliant delivery of ProductArtworkAutomationthat meetsall HA and company innovative technology bestpracticesand synergies for operational/ automationefficiency in compliance with J&J Policy and local HA Requirements.

She/He will establish and lead cross-functional automated artworktemplate governance to drive andmaintainstandardization ensuring robust control over automated artworktemplate designand usage. Assess andmanagethe impact of change requests to safeguard compliance minimize risk and sustaintemplateefficiency.

They will be responsible for the design design review and enhanceProduct Artworktechnical and automation processes; establish KPIs tomonitorperformance and value creation.

She/he will work closely with stakeholders to include IT Regulatory Quality Packaging Sites Brand Protection Supply Chain and external partners/ vendorsto drive seamless automation integration;and deliver proactive expert technical support for all artwork-related willbuild andmaintaina high-performing inclusive team culture; coach and develop talent while fostering a ourCredo-based environment. They will ensure adherence to artwork systems and regulatory standards; proactivelyidentifyand mitigate technical and automation risks.

She/He will work with PA LT to managedepartmental budgetsoptimizeresource allocation and manage workload will benchmark best practices strengthen internal capabilities andleverageexternal partnerships for non-core will continuously reportprogress challenges and achievements to senior leadership and stakeholders.

Qualifications:

Education:

Bachelors degreerequired; MBA or advanced degree in Engineering Business or Supply Chain preferred.

Experience & Skills (Required):

• A minimum of 10 years of relevant experience in a Pharmaceutical / regulated environment.

• Technical & automation related experience in artwork or packaging fields.

• Experience incoordinating /troubleshooting artwork Regulatory Labeling& packaging design.

• 4 yearspeople managementexperiencein a diverse and multicultural environmentcoaching and developing employees communicatinga clear visionand strategy and leading a team through a change managementjourney.

• At least4years exposure to and general understanding of regulatory processes and systems and/or in pharmaceutical packaging artwork management or related fields.

• Strong understanding of regulatory requirementspertaining toartworkpackagingand labeling in the pharmaceutical industry.

• Supply Chain experience includingexpertisein value chainpackaging sitesMSAT external vendor management and/or related areas

• Knowledgeofartwork 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 strongdemonstratedstakeholder management

• Experience with guides and regulations as well as industry technical standards related toartworkincluding experience with international and pharmaceutical regulatory authorities. Knowledge &expertisein 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 anddemonstrateresiliency and high productivity with constraints of schedule and budge

• 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 (/ Esko)

Experience insetting upKPIs and managing departmental budgets.

Experience in familiarity with design software tools( Illustrator)