Назад
Company hidden
4 дня назад

Project Manager (Pharmaceutical)

90 000 - 120 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US/Switzerland
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
Project Manager (Pharmaceutical): Leading complex pharmaceutical new product development, introduction, and customer-driven CDMO projects across feasibility, development, manufacturing, and aftercare with an accent on scope, schedule, cost, quality, and regulatory compliance. Focus on coordinating cross-functional teams, managing technical transfers and plant readiness, resolving project risks, and delivering projects under cGMP, FDA, environmental, and process safety requirements.

Location: Athens, United States; onsite role with up to 25% travel to other facility locations

Target salary range: $90,000–$120,000 per year

Company

hirify.global is a global pharmaceutical contract development and manufacturing organization (CDMO) developing and manufacturing APIs and finished dosage forms across a network of 16 sites and three continents.

What you will do

  • Lead complex new product development and introduction programs through all seven NPI/NPD stages, from feasibility to aftercare.
  • Manage customer-driven CDMO projects, including proposals, deliverables, milestones, budgets, risks, and interdependencies.
  • Build and coordinate multidisciplinary project teams and facilitate communication with customers, suppliers, operations, and senior management.
  • Coordinate scheduling, permits, capital appropriation, plant readiness, documentation, and SAP setup for new products.
  • Review development and production documentation, test procedures, drug master file sections, validation materials, and regulatory submissions.
  • Lead technical transfers from development to internal or external production while ensuring cGMP, safety, environmental, and quality requirements.

Requirements

  • Bachelor’s degree in Chemistry, Chemical Engineering, or a related field.
  • At least 6 years of experience in the pharmaceutical or biotech industry.
  • Experience with pharmaceutical active ingredient manufacturing, drug development, drug technology, and project management processes.
  • Previous experience with cGMPs at an FDA-regulated site, process safety practices, and environmental standards.
  • Ability to manage multiple priorities, communicate technical information to non-technical audiences, and work autonomously with minimal supervision.
  • Strong computer skills, including hands-on experience with Microsoft Office, Excel, Word, and Project.

Nice to have

  • Advanced education in a relevant field.
  • Project management professional or business excellence certification.
  • Experience with commercial process improvement projects, line extensions, or external manufacturing networks.

Culture & Benefits

  • Medical, dental, and vision coverage.
  • Flexible Spending Account and HSA options.
  • Life insurance and short- and long-term disability coverage.
  • Pet insurance, generous PTO, sick leave, and holiday time off.
  • 401(k) plan and opportunities for professional growth in a global pharmaceutical organization.

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 →