14 сен

project manager in pharma manufacturing

ориентир по рынку
вакансия зп не указана
в среднем 236 267 ₽
Загрузи резюме, чтобы видеть мэтчи с вакансией

подготовьтесь к отклику

ai-инструменты

Чтобы адаптировать резюме под вакансию или составить сопроводительное письмо, загрузите резюме

описание

The company provides IT services and IT consulting.

задачи

  • Lead large, complex pharma programs involving manufacturing, supply chain, operational sites, and technology/application implementations;
  • Develop and manage project plans, milestones, dependencies, resources, governance, RAID logs, risks/issues, and executive reporting;
  • Drive application/system deployment and site readiness across manufacturing or supply chain sites;
  • Work directly with site teams to drive actions, resolve roadblocks, manage competing priorities, and ensure implementation readiness;
  • Identify and manage project and operational risks, develop mitigation plans, escalate appropriately, and drive issues to closure;
  • Coordinate cross-functional stakeholders across business, IT, manufacturing, supply chain, quality, and site leadership;
  • Drive change management, including stakeholder alignment, communications, training, adoption, and resistance management;
  • Support new product launch and commercialization activities, including manufacturing and supply-chain readiness where applicable;
  • Communicate project status, risks, decisions, and recommendations clearly to senior leadership.

требования

  • Senior project or program management experience within pharma or biopharma;
  • Experience in pharma supply chain or manufacturing operations;
  • Experience with application/system implementation or deployment at operational or manufacturing sites;
  • Experience with PMO governance and program execution;
  • Experience in risk and issue management;
  • Experience with RAID logs and risk registers;
  • Experience in dependency and milestone management;
  • Experience with site readiness and operational deployment;
  • Experience in a pharma/GxP regulated environment;
  • Validation, change control, CAPA, and compliance exposure;
  • Strong stakeholder and executive management skills;
  • QA or QC experience is acceptable;
  • Nice to have: multi-site implementation or rollout experience, new product launches, commercialization, manufacturing or supply-chain launch readiness.

условия

  • 100% Remote;
  • USA EST working hours;
  • Contract for 12+ months;
  • 40 Hours per week / 8 hours per day.

Если просят выйти из iCloud, прислать код из SMS, запустить или установить что-то, перевести деньги — не соглашайтесь: это мошенничество.

Про зарплаты

Анонимные данные по зарплатам и грейдам.
Можно сверить вилку с рынком.

Посмотреть зарплаты

Если просят выйти из iCloud, прислать код из SMS, запустить или установить что-то, перевести деньги — не соглашайтесь: это мошенничество.