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5 дней назад

Director, US Quality (Analytical Technical Solutions) Lead (Pharmaceutical Quality)

156 900 - 247 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Релокация
US
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
Director, US Quality (Analytical Technical Solutions) Lead (Pharmaceutical Quality): Leading analytical technical solutions and quality project portfolios across pharmaceutical manufacturing sites with an accent on team development, analytical method lifecycle management, and cross-functional execution. Focus on planning complex analytical programs, resolving delivery and quality gaps, and aligning stakeholders across manufacturing, quality, operations, and commercialization.

Location: Hybrid role based in De Soto, Kansas, USA; relocation is domestic. Applications are limited to US and Puerto Rico residents.

Salary: $156,900–$247,000 annual base salary for the primary location, plus potential annual bonus and long-term incentive.

Company

hirify.global’s Animal Health Division develops veterinary pharmaceuticals, vaccines, health-management solutions, and related services for veterinarians, farmers, pet owners, and governments.

What you will do

  • Lead and develop the US Analytical Technical Solutions organization, including organizational design, staffing, budget planning, hiring, governance, and coaching.
  • Plan and execute the analytical project portfolio across multiple sites and platforms.
  • Coordinate cross-functional execution, milestones, metrics, reporting, governance meetings, and issue resolution.
  • Act as the primary partner for analytical topics, align priorities with site management, quality operations, and regional leaders, and represent progress to senior leadership.
  • Oversee analytical support activities including method remediation, robustness and improvement, site-to-site transfers, and new product commercialization transfers.

Requirements

  • Bachelor’s degree in analytical, pharmaceutical, biopharmaceutical, biological, or analytical science, or equivalent experience; a master’s degree is preferred.
  • 10–15 years of experience in the research, manufacture, and testing of pharmaceutical and/or biological products, including sound knowledge of key analytical technologies.
  • Experience with analytical method development, validation, robustness, and transfer.
  • Proven experience shaping, developing, and leading multiple teams and employees in matrix organizations.
  • Strong project execution and leadership skills, including leading multifaceted projects in complex environments.
  • Strong communication, networking, behavioral, advocacy, lobbying, and alliance-building skills.
  • End-to-end understanding of pharmaceutical business processes and holistic thinking.
  • Flexibility in working schedules and willingness to travel; travel is expected at 25%.
  • A valid driving license is required.

Nice to have

  • Regulatory compliance experience.

Culture & Benefits

  • Hybrid work arrangement with first-shift daytime hours.
  • Inclusive environment that encourages respectful challenge, collaboration, initiative, and diverse perspectives.
  • Medical, dental, vision, and other insurance benefits for employees and families.
  • Retirement benefits including 401(k), paid holidays, vacation, and compassionate and sick days.
  • Regular employee status with long-term career perspectives.

Hiring process

  • Applications are accepted through the hirify.global careers application process; current employees and contingent workers have separate application routes.
  • Visa sponsorship is not available.

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