Senior Business Quality Specialist
Вакансия № 108867 от компании Johnson & Johnson на Электронной Службе Занятости Населения Москвы.
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☑ Основной блок:
Опыт работы: 3–6 лет.
Тип занятости: полная занятость.
График работы: полный день.
Зарплата: по результату собеседования.
Место работы (точный адрес): Россия, Москва, Крылатская улица, 17К3, м. Крылатское.
☑ Актуальность объявления:
Это объявление № 108867 добавлено в базу данных: Четверг, 6 февраля 2025 года.
Дата его обновления на этом интернет-ресурсе: Воскресенье, 16 марта 2025 года.
☑ Статистика предложения работы № 108867:
Прочитано соискателями - 260 раз(а);
Отправлено откликов - 0 раз(а);
☑ Репутация компании "Johnson & Johnson":
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☑ Подробности о вакантном месте:
Johnson & Johnson (Medical Devices division) is looking for a strong candidate with communication and interpersonal skills, team-oriented, self-motivated, multi-task management and problem-solving abilities for Senior Business Quality Specialist role based in Moscow, Russia.
Reporting line: Business Quality Lead, Russia & CIS
Senior Business Quality Specialist will support development and maintenance of the local Quality Management System. Role will be responsible for various QA activities, such as maintenance and execution of Internal Quality Audit Program and driving process improvements, addressing CAPA (Corrective action Preventive Actions).
Ensures effective communication and training are deployed throughout the Organization on Quality Management System elements. This position will report to Quality function.
Main Responsibilities:
- Ensures the maintenance of quality records, nonconformance, project outcomes, and that stakeholder input is filed in an accurate and timely manner
- Management and Review of the change control process, tracks the approval process / action execution
- Contributes to the development of corrective action / preventive action plans and monitors implementation
- Management of the nonconformance
- Reports on execution and closure of corrective and preventive actions, nonconformance, strong cooperation with CAPA, NC Owners
- Performs GAP assessment evaluation against corporate standards and support process improvement implementation
- Monitors and Leads investigations, recognizes trends and presents reports for assigned quality processes
- Reviews reports on current quality systems and supports improvements in order to enhance quality
- Execution of Internal Audits within Company, assures preparation for External Audits and Health Authorities Inspections
- Support Escalation process of Quality Compliance matters
- Monitors trends, identifies issues, recommends and implements appropriate actions
- Develops implements and reviews Standard Operating Procedures, Work Instruction and other Quality Documentation
- Provide Quality support in Supplier Management process, assessment of suppliers based on Quality Assurance criteria, company quality policy, standards and local regulations
- Management of product complaints, timely reporting into local system, data trending.
- Handling Customer Complaints
Requirements:
- Higher education
- 2 years+ experience in Quality Assurance within Pharmaceutical, Medical Devices or FMCG business
- Knowledge of GMP and GDP preferred
- It is preferred that the job holder is an experienced internal auditor or certifies lead auditor
- English on upper-intermediate level as a must
- Excellent interpersonal, collaboration, networking and communication skills
- Readiness for business trips
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