
Regulatory Affairs Manager
Almaty, Almaty- Job Type: Full Time
- Job Level: Senior
- Travel: Minimal (if any)
Takeda has been translating science into breakthrough medicines for 240 years. Every step of the way, our teams have worked together to tackle some of the most challenging problems in drug discovery and development. Today, we’re a driving force behind innovative therapies that make a lasting difference to millions of patients around the world.
In R&D, all of our history and potential comes together in an environment that welcomes diversity of thought and amplifies every voice. Working closely with colleagues, you’ll play a key role in bringing our rich pipeline of products forward to help patients. Come join a team that’s earned trust for more than two centuries, and find out how advancing transformative therapies at Takeda will shape your bright future.
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Job Description
Job Title: Regulatory Affairs Manager
Location: Kazakhstan, Almaty
How you will contribute:
- Осуществление регистрации/ перерегистрации/ внесения изменений лекарственных препаратов в соответствии с местными нормативными актами и/или законодательством ЕАЭС.
- Запрос рег. досье у производителя, подготовка, подача в РО и отслеживание этапов экспертизы.
- Разработка и согласование локальных регистрационных документов, таких как инструкция по применению, макеты упаковок с подразделениями Компании/странами ЕАЭС/производственной площадкой;
- Взаимодействие с ГО для своевременного утверждения регистрации/ перерегистрации/ внесения изменений.
- Взаимодействие с коллегами из ЕАЭС стран ( РФ, РБ) для планирования, подачи и утверждения процедур приведения в соответствие/внесение изменений согласно правилам ЕАЭС.
- Взаимодействие с глобальной командой регистрации и производителем для планирования, подачи, подготовки досье и ответа на запросы РО.
- Техническая поддержка менеджеру по регистрации в отношении глобальных регуляторных систем, а именно ведение и своевременное обновление базы данных.
- Заключение договоров с РО на экспертизу, обеспечение оплаты всех пошлин;
- Одобрение промоционных и медицинских материалов;
- Отслеживание и подача в РО Периодических Отчетов о Безопасности (ПООБ);
- Обеспечивать координацию работы департамента со структурными подразделениями Компании и осуществлять регуляторную поддержку кросс-функциональных проектов;
What you bring to Takeda:
- высшее образование и стаж работы не менее двух лет в сфере регистрации лекарственных средств
- опыт подач по ЕАЭС законодательству
- уровень английского языка не ниже Up-intermediate (В2)
- хорошее владение ПК, технические навыки для работы в компьютерных системах и базах данных
- умение быстро обучаться
- хорошие коммуникационные и организаторские навыки
- умение работать в команде
More about us:
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Empowering our people to shine:
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations
Almaty, KazakhstanWorker Type
EmployeeWorker Sub-Type
Fixed Term (Fixed Term)Time Type
Full timeThe heart of our work
Shining a light on new perspectives
Working at Takeda
-
Inclusion
Here, you will feel welcomed, respected, and valued as a vital contributor to our global team. -
Collaboration
A strong, borderless team, we strive together towards our priorities and inspiring mission. -
Innovation
Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients. -
Top Workplace
Recognized for our culture and way of working, we’re one of only 17 companies to receive Top Global Employer® status for 2024. -
Work-Life
Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family. -
Empowerment
Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
We're Steadfast In Our Commitment to Four Key Imperatives
Patient
Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
People
Create an exceptional people experience.
Planet
Protect our planet.
Data & Digital
Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.
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