Назад
Company hidden
15 часов назад

Associate Director, CDMO Alliance Management (Pharmaceutical Manufacturing)

169 222 - 253 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Associate Director, CDMO Alliance Management (Pharmaceutical Manufacturing): Managing the end-to-end lifecycle of contract development and manufacturing organization partnerships with an accent on strategic sourcing, contract negotiation, governance, and supplier performance. Focus on strengthening supply-chain resilience, assessing GMP and operational risks, and coordinating cross-functional responses to manufacturing incidents and disruptions.

Location: Princeton, NJ, United States

Salary: $169,222–$253,000 annually, plus incentive opportunity.

Company

hirify.global is a pharmaceutical company developing and delivering healthcare products and services.

What you will do

  • Act as the central business partner and point of contact for Contract Development and Manufacturing Organizations (CDMOs).
  • Lead partner selection, contract negotiations, governance structures, and executive business reviews.
  • Define and monitor KPIs covering CDMO delivery, quality, and operational performance.
  • Assess supply-chain and partner-site risks and drive improvement measures based on performance data.
  • Coordinate cross-functional responses to major incidents, regulatory changes, demand volatility, and manufacturing deviations.
  • Support decisions on new CDMO selections and major capital investments, including business-side assessments during GMP audits.

Requirements

  • Bachelor’s degree in Science, Engineering, Business, or a related field; an MBA or advanced degree is preferred.
  • 8–12+ years of experience in alliance management, strategic sourcing, or external manufacturing in the pharmaceutical or biotech industry.
  • Experience influencing and collaborating with stakeholders in complex, matrixed organizations and with international colleagues.
  • Strong expertise in risk management, business continuity planning, KPI-based performance analytics, negotiation, and supplier relationship management.
  • Knowledge of the CDMO landscape and manufacturing processes across modalities such as small molecules, biologics, and sterile fill-finish.
  • Thorough knowledge of GMP requirements, including CFR Title 21 Parts 210–211 and Part 600, as well as EU, MHRA, and other global health authority regulations.

Culture & Benefits

  • Comprehensive medical, dental, vision, and prescription drug coverage.
  • Company-provided life, accidental death and dismemberment, and short- and long-term disability insurance.
  • Tuition reimbursement and student loan assistance.
  • Generous 401(k) match, flexible time off, paid holidays, and paid leave programs.
  • Culture emphasizing accountability, strategic problem solving, patient and customer centricity, impactful communication, respectful collaboration, and professional development.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →