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2 часа назад

Associate Director, Process & Analytical Development (Pharmaceutical Manufacturing)

155 700 - 181 650$
Формат работы
remote (только USA)/onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
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
Associate Director, Process & Analytical Development (Pharmaceutical Manufacturing): Leading process and analytical development, project-specific manufacturing activities, and organizational readiness for future pharmaceutical manufacturing operations with an accent on GMP compliance, technology transfer, validation, and scale-up. Focus on building high-performing teams, planning capacity and resources, driving Lean and digital transformation, and coordinating complex facility startup and expansion initiatives.

Location: Initially remote in the United States; transition to an on-site U.S. East Coast or Midwest location is anticipated as the project progresses, expected in 2027. Monday–Friday, 8:00 a.m.–5:00 p.m.

Salary: $155,700–$181,650 gross annual base salary, plus performance-related bonus.

Company

hirify.global operates more than 30 sites across five continents and supports the development and manufacturing of medicines and life-science products.

What you will do

  • Lead, coach, and develop the Process & Analytical Development team while building accountability, collaboration, safety, and continuous improvement.
  • Set strategic direction through long-range planning, portfolio prioritization, resource allocation, budgeting, and performance management.
  • Ensure process development, analytical development, and project-specific manufacturing activities are delivered safely, compliantly, on time, in full, and within budget.
  • Support Sales & Operations Planning by aligning capabilities, capacity, and organizational structures with customer demand.
  • Lead facility startup, operational readiness, validation, manufacturing scale-up, technology transfer, and process development initiatives.
  • Drive Lean maturity, digital tools, automation, data-driven decision-making, governance, risk management, and succession planning.

Requirements

  • Master’s degree in engineering, life sciences, pharmaceutical sciences, chemistry, biochemistry, or a related scientific discipline.
  • At least 10 years of progressive leadership experience in pharmaceutical, biotechnology, process development, analytical development, or manufacturing operations.
  • Deep understanding of small-molecule and bioconjugate technologies, small-molecule drug-substance manufacturing, GMP environments, and pharmaceutical commercialization.
  • Experience with facility startups, technology transfers, validation programs, operational readiness, greenfield or brownfield expansions, and large-scale capital projects.
  • Ability to lead cross-functional work with Engineering, Quality, Manufacturing, MSAT, Automation, EH&S, Finance, and Human Resources.
  • Knowledge of Lean Manufacturing, Six Sigma, digital systems, automation technologies, and data integrity principles, with strong executive communication and problem-solving skills.

Culture & Benefits

  • Performance-related bonus.
  • Medical, dental, and vision insurance.
  • 401(k) matching plan.
  • Life insurance and short- and long-term disability insurance.
  • Employee assistance programs and paid time off.
  • Culture centered on collaboration, accountability, excellence, passion, integrity, safety, and innovation.

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