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7 дней назад

Sr. Specialist, Project Management - Chemistry Manufacturing & Controls (CMC) (Hybrid)

117 000 - 184 200$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
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
Sr. Specialist, Project Management - Chemistry Manufacturing & Controls (CMC) (Hybrid) (CMC/drug and vaccine development): Managing integrated project plans and cross-functional development teams across the CMC continuum from Line of Sight to First in Human and Transfer to Supply, with an accent on project strategy, commercialization, and lifecycle management. Focus on building schedules, identifying risks, facilitating governance and team decisions, and removing obstacles across complex development programs.

Location: Hybrid; primary location in Rahway, New Jersey, United States. This posting is for residents of the United States, Canada, and Puerto Rico.

Salary: $117,000–$184,200 annually for the primary location; annual bonus and long-term incentive may also apply.

Company

hirify.global develops medicines and vaccines through its Research and Development organization.

What you will do

  • Manage moderate-complexity CMC development projects or support higher-complexity development strategies and plans.
  • Guide teams in creating, approving, and executing integrated project plans across development phases.
  • Build project schedules, integrate cross-functional activities, identify risks, and maintain critical project information.
  • Facilitate key team meetings, align stakeholders, provide project management insights, and follow up on decisions and actions.
  • Navigate corporate governance and business requirements to support informed decision-making.
  • Participate in CIPM and Global Project and Alliance Management initiatives and workstreams.

Requirements

  • Bachelor’s degree required; a scientific or applied discipline is preferred.
  • At least 3 years of experience in project management or a related role required.
  • Experience planning and executing strategies for drug or vaccine product registration, commercialization, or lifecycle management from an R&D, manufacturing, or commercial perspective.
  • Ability to translate relevant knowledge and expertise to other development teams and areas.
  • Ability to work independently, serve as a resource for colleagues and program teams, and collaborate effectively across diverse teams and networks.
  • Strong organization, attention to detail, problem-solving, communication, alignment-building, and issue-escalation skills.
  • Ability to adapt and respond effectively to changing priorities in a dynamic environment.

Nice to have

  • Clinical drug development experience and knowledge, including development phases and functional-area contributions to comprehensive strategies.
  • PMP certification or formal project management coursework or training.

Culture & Benefits

  • Hybrid work arrangement with 10% travel.
  • Regular employee status with medical, dental, vision, insurance, retirement benefits including 401(k), paid holidays, vacation, compassionate leave, and sick days.
  • Inclusive environment that values diverse experiences, respectful challenge, collaboration, and collective problem-solving.
  • Visa sponsorship is not available and relocation is not provided.

Hiring process

  • Applications are accepted until the day before the listed posting end date of November 11, 2026.
  • Current employees and contingent workers must apply through the designated internal application routes.

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