3 дня назад
Project Manager (Pharmaceutical CDMO)
90 000 - 120 000$
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Project Manager (Pharmaceutical CDMO): Leading complex new product development, introduction, and customer-driven CDMO projects across pharmaceutical manufacturing with an accent on scope, schedule, cost, quality, regulatory compliance, and cross-functional coordination. Focus on managing NPI/NPD programs through all stages, coordinating technical transfers and plant readiness, resolving project risks and interdependencies, and presenting status to senior management.
Location: Athens, Greece
Target salary range: $90,000–$120,000 per year
Company
Founded in 1873, is a global pharmaceutical CDMO developing and manufacturing active pharmaceutical ingredients and finished dosage forms across 16 sites.
What you will do
- Lead complex new product development and introduction programs through all seven NPI/NPD stages.
- Manage customer-driven CDMO projects from kick-off through completion, coordinating cross-functional and external manufacturing teams.
- Control project scope, schedules, budgets, risks, quality attributes, milestones, action items, and interdependencies.
- Coordinate plant readiness, permits, capital appropriation, documentation, production scheduling, and SAP setup for new products.
- Lead technical transfers from development to internal or external production and support validation and regulatory submissions.
- Prepare project updates for senior management and facilitate communication with customers, suppliers, and internal stakeholders.
Requirements
- Bachelor’s degree in Chemistry, Chemical Engineering, or a related field.
- At least 6 years of experience in the pharmaceutical or biotechnology industry.
- Experience with pharmaceutical active ingredient manufacturing, drug development, drug technology, and project management processes.
- Experience with cGMPs at an FDA-regulated site, process safety practices, and environmental standards.
- Ability to manage multiple priorities, communicate technical information clearly, and work autonomously.
- Hands-on experience with Microsoft Office, including Excel, Word, and Project.
Nice to have
- Advanced education in a relevant field.
- Project management professional or business excellence certification.
Culture & Benefits
- Collaborative environment focused on safety, quality, sustainability, and professional growth.
- Medical, dental, and vision insurance.
- Flexible Spending Account and HSA options, life insurance, disability coverage, and pet insurance.
- Generous paid time off, sick leave, holiday time off, and 401(k).
- Up to 25% travel may be required for introductions at other facility locations.
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