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9 дней назад

Contract Development & Mfg Sr Mgr (Biotech Manufacturing)

101 613 - 137 477€
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Contract Development & Mfg Sr Mgr (Biotech Manufacturing): Leading contract manufacturing operations, site performance, budgets, agreements, capacity planning, and product technology transfers for pharmaceutical products with an accent on cGMP compliance, operational excellence, and cross-functional coordination. Focus on managing contract manufacturing organizations, resolving site issues, transferring products across locations, and driving risk-based improvements.

Location: Dublin, Ireland; travel required approximately 20% domestically and internationally.

Salary: €101,613.25–€137,476.75 per year, plus a competitive total rewards package aligned with local industry standards.

Company

hirify.global is a biotechnology company researching, manufacturing, and delivering medicines for serious diseases.

What you will do

  • Lead manufacturing operations and business processes for contract manufacturing sites.
  • Manage relationships, contracts, budgets, forecasts, financial performance, and capacity planning with contract manufacturing organizations.
  • Monitor site performance through lean tools, PDCA, operating reviews, and continuous improvement initiatives.
  • Lead cross-functional projects from conception through implementation and close-out.
  • Oversee product technology transfers, including budgets, timelines, risk management, issue resolution, and executive escalation.

Requirements

  • Bachelor’s degree in business administration, engineering, science, or a related field.
  • 8+ years of experience in protein, API, drug substance, drug product, or packaging manufacturing.
  • 8+ years of experience with cGMP principles, FDA and other regulatory guidelines, and validation principles.
  • 5+ years of experience working with external parties or leading cross-functional teams for clinical or commercial products.
  • 3+ years of project management experience with multi-functional and multi-location teams, plus experience across ACM or CMQ.
  • Ability to travel approximately 20% of the time, including domestic and international travel.

Culture & Benefits

  • Collaborative, innovative, and science-based working environment.
  • Competitive and comprehensive total rewards plans aligned with local industry standards.
  • Support for professional growth, personal well-being, and career development.
  • Inclusive workplace based on ethical conduct, respect, and equal opportunity.

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