обновлено 5 дней назад
Development Manager II (Small Molecule CMC)
60 750 - 85 050€
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
Development Manager II (Small Molecule CMC) (pharmaceutical development and manufacturing): Defining development strategies and managing scalable production and supply of small molecule technology components with an accent on CMC, GMP manufacturing, and external partner management. Focus on coordinating CDMOs, regulatory documentation, process scale-up, and reliable supply for clinical development programs.
Location: Oss, Netherlands
Annual base salary: €60,750–€85,050
Company
A global life sciences company developing and manufacturing technologies and medicines across more than 30 sites worldwide.
What you will do
- Define development strategies, roadmaps, milestones, and budgets for assigned small molecule technology components.
- Own the development and manufacturing processes, including scalable production, testing, release activities, and process and analytical development.
- Manage CDMOs, CROs, vendors, and external partners, including vendor selection, contract negotiations, manufacturing campaigns, and supply planning.
- Prepare and review regulatory, quality, financial, and compliance documentation in collaboration with cross-functional stakeholders.
- Support technical relationships with licensees and align component supply with clinical development requirements and demand forecasts.
- Mentor junior colleagues, coordinate subject matter experts, and support continuous improvement initiatives.
Requirements
- PhD in Chemistry, Organic Chemistry, Pharmaceutical Chemistry, or a related discipline.
- 5–10 years of industry experience in pharmaceutical development, process development, CMC, or GMP manufacturing.
- Strong knowledge of synthetic organic chemistry and pharmaceutical manufacturing processes.
- Experience with project and program management, including planning, budgeting, prioritization, and execution of parallel activities.
- Experience managing external development and manufacturing partners, including CDMOs and CROs.
- Knowledge of GMP manufacturing, ICH guidelines, pharmaceutical regulatory requirements, and cross-functional team leadership.
Nice to have
- Hands-on experience in small molecule API process development, process scale-up, and GMP manufacturing.
- Experience with CMC development and manufacturing of ADC linker-payloads, HPAPIs, or related technologies.
Culture & Benefits
- Agile career environment and dynamic working culture.
- Inclusive and ethical workplace.
- Performance-based compensation programs.
- Benefits provided according to role and location.
- Collaborative, accountable, excellence-focused, and diverse international work environment.
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