Вакансия: Quality Assurance Manager

от компании (организации): Сarl Zeiss в городе (населенном пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Регистратура"
с оплатой труда: по договоренности

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Вакансия № 21554724 добавлена в базу данных сайта Электронный Центр Занятости Населения: Вторник, 13 мая 2025 года.
Дата обновления вакансии № 21554724 на сайте Электронного Центра Занятости Населения: Воскресенье, 29 июня 2025 года.

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Требования к опыту работы: 1–3 года
Тип занятости: полная занятость
График работы: полный день

Дополнительные сведения о вакансии: Quality Assurance Manager

ZEISS Russia & CIS develops and distributes technological solutions to science, education, innovation industry, manufacturing, and health service in Russia, the CIS countries & Ukraine.

As an international company, ZEISS Russia & CIS applies the Code of Conduct. It summarizes the general rules of conduct regarding various aspects of our business activities.

We are convinced that the success of the Company depends on each employee. Therefore we are focused on cooperation with professionals who combine enthusiasm, striving for perfection, flexibility of thinking and passion for innovation.
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We invite you to join our team as a Quality Assurance Manager.

Mail responsibilities:

Region of responsibility: Russia, Ukraine, Armenia, Belarus, Kazakhstan, Kyrgyzstan

• Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with corporate policies and that the performance and quality of services conform to established internal and external standards and guidelines.
• Leads audit and inspection preparation findings and liaises with auditing groups. Accompanies internal and external auditors\inspectors through all stages of the audits.
• Drive the improvement process in Quality field.
• To define, develop, revise internal program, working instructions, procedures etc. to assure compliance with global policy and local regulation.
• Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations to assure compliance.
• To prepare reports and/or necessary documentation and provides to applicable stakeholders, both internal and external.
• To establish Complaints Handling process.
• To perform Vigilance (Medical Device Reporting) process including data analysis, gathering information, reporting to the local Competent Authority.
• To perform action in the region regarding FSCA (including reporting to the local Competent Authority).

Requirements:

• Higher education, scientific background is a plus (Biology, Chemistry, Medical devices, Pharma).
• Knowledge of ISO 13485, ISO 9001.
• Experience in building Quality Management System, developing processes, procedures and complaints handling at least 3 year.
• Practice in developing SOPs, processes, working instructions.
• English - Upper-Intermediate (writing, speaking).
• Excellent interpersonal, collaboration, networking and communication skills.
• Leadership competencies.
• Analytical skills, strong decision making, high motivation.

Conditions:

• Competitive salary and bonus system.
• Medical insurance.
• Meal allowance.
• Mobile communication compensation.
• Comfortable office.
• Great opportunities for professional and career growth.

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Предыдущая вакансия:
Вакансия № 21554725 на должность Менеджер по работе с клиентами от компании Гранд Проект в городе (населенном пункте) Москва