Назад
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6 дней назад

Associate Director, Product Artwork Management (Biotechnology)

Тип работы
fulltime
Грейд
director
Английский
b2
Страна
Ireland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Director, Product Artwork Management (Biotechnology): Building and scaling a governed product artwork capability for printed packaging components, including labels, cartons, and leaflets, across development, commercialization, and lifecycle management with an accent on regulatory compliance, quality, and on-time delivery. Focus on designing the operating model, establishing inspection-ready governance, standardizing artwork processes, and developing a high-performing cross-functional team.

Location: Ireland

Company

hirify.global is a biotechnology company developing therapies for genetically defined rare diseases and manufacturing medicines for patients worldwide.

What you will do

  • Lead the end-to-end product artwork capability across development, commercialization, and lifecycle management.
  • Set the strategy and operating model for product artwork management across hirify.global's product portfolios.
  • Design and scale standardized processes for labels, cartons, leaflets, and other printed packaging components.
  • Establish inspection-ready governance to support accurate, compliant, and timely artwork delivery in every market.
  • Serve as the artwork and labeling subject-matter expert and cross-functional integrator across Regulatory Affairs, Quality, Technical Operations, Supply Chain, Manufacturing, and Commercial.
  • Build and develop a high-performing artwork management team and enable successful launches and uninterrupted product supply.

Requirements

  • Deep expertise in product artwork and labeling management across the product lifecycle.
  • Strong regulatory and quality expertise within a biotechnology, pharmaceutical, or related manufacturing environment.
  • Experience designing operating models, standardized processes, and governance frameworks.
  • Ability to collaborate across Regulatory Affairs, Quality, Technical Operations, Supply Chain, Manufacturing, and Commercial functions.
  • Commitment to environmental protection, injury prevention, hazard identification, incident reporting, and EHS initiatives in Ireland.

Culture & Benefits

  • Work within a global biotechnology organization focused on rare disease therapies.
  • Collaborate with multidisciplinary teams supporting clinical development and commercial manufacturing.
  • Contribute to a safe and environmentally responsible workplace.
  • Participate in EHS training and continual improvement initiatives.

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