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1 день назад

Project Manager I (Biomanufacturing)

80 000 - 121 250$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Project Manager I (Biomanufacturing): Supporting client-facing drug manufacturing projects across technical transfer, development, manufacturing, and supply chain activities with an accent on project coordination, GMP compliance, and stakeholder communication. Focus on managing schedules, tracking risks and changes, coordinating cross-functional teams, and maintaining client deliverables through the project lifecycle.

Location: West Chester, Ohio, USA

Base pay: $80,000–$121,250 per year

Company

hirify.global is a technology-focused biomanufacturing company building a sustainable network of end-to-end manufacturing solutions for medicines.

What you will do

  • Manage assigned client-facing projects from initiation through completion.
  • Develop project plans, timelines, action-item logs, status reports, and project documentation.
  • Coordinate technical transfer, manufacturing readiness, development, and supply chain activities.
  • Act as the day-to-day client contact, facilitate project meetings, and communicate progress, risks, and milestones.
  • Coordinate Manufacturing, Quality, Supply Chain, MS&T, Regulatory Affairs, and Product Development teams.
  • Track budgets, forecasts, scope changes, risks, mitigation plans, and project commitments.

Requirements

  • Experience in project coordination, project management, manufacturing, development, or operations within biotechnology, pharmaceutical, CDMO, or related industries.
  • Understanding of pharmaceutical manufacturing processes and GMP requirements.
  • Strong organizational, communication, and stakeholder management skills with the ability to manage multiple priorities.
  • Experience with project management tools such as Microsoft Project, Smartsheet, or an equivalent platform.
  • Ability to meet the role's visual and computer-use requirements, including reading reports and documents and distinguishing colors.
  • Work authorization or visa sponsorship is not available for this position.

Nice to have

  • 2–4 years of relevant experience in biotechnology, pharmaceuticals, CDMO, CRO, manufacturing, development, or operations.
  • Bachelor’s degree in Life Sciences, Engineering, Pharmaceutical Sciences, Business, or a related discipline.
  • Experience with technical transfer, clinical manufacturing, commercial manufacturing, or the drug development lifecycle.
  • PMP certification or project management training.

Culture & Benefits

  • Annual cash bonus program and 401(k) plan with company match.
  • Medical, dental, and vision coverage, plus life and disability insurance.
  • Paid vacation, paid holidays, and other paid leaves of absence.
  • Tuition reimbursement, family-building benefits, and caregiving support.

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