Вакансия № 1663654 на Электронной Службе Занятости Населения от компании Рост Групп на должность Специалист по GMP в населенном пункте Киев

☑ Основы вакансии:

Опыт работы: 3–6 лет.

Тип занятости: полная занятость.

График работы: полный день.

Зарплата: по результату собеседования.

Примерное место работы: Украина, Киев.

☑ Актуальность объявления:

Это объявление № 1663654 добавлено в базу данных: Воскресенье, 31 марта 2024 года.

Дата его обновления на этом интернет-ресурсе: Вторник, 23 апреля 2024 года.

☑ Репутация компании "Рост Групп":

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☑ Подробности о вакантном месте:

International pharmaceutical company announces vacancy of Head GMP.

Main responsibilities:

• Management of Ukrainian GMP certification
• Preparation of the full set of documents required for GMP certification and getting documents of acceptance of the results inspection PIC/S countries (GMP Conclusion), updating list of products for GMP Certificates or GMP Conclusions.
• Coordination Ukrainian GMP certification incl. inspections of the company and its affiliates and contract manufacturing sites
• To coordinate and if necessary to participate in GMP inspections of the company and its affiliates and contract manufacturing sites;
• To coordinate CAPA availability and advise on fulfillment;
• Planning of the inspection schedule, accompaniment of the inspectors, tracking of the documentation at the end of the circle, follow up for CAPA;
• To coordinate GMP submissions for the Company and its affiliates as well as contract manufacturing sites;
• Ensure continuous import of medicinal products in the company distribution.
• Conducting/coordinating audits of the company and its affiliates and contract manufacturing sites
• Participation in GMP audits of the company and its affiliate companies as well as contract manufacturing sites;
• Update of GMP certificates as necessary;
• Ensure assessment of the company and its affiliates for compliance with GMP and Global Procedures.
• Internal and external audits and inspections, and quality reviews
• To perform audits of third-party suppliers/subcontractors for all GXP and health-regulated activities directly or through an associate;
• To ensure any time audit/inspection readiness;
• To conduct internal audits and inspections for all GXP and health-regulated activities directly or through an associate;
• To carry-out periodic quality reviews (meetings);
• Ensure any time audit readiness of the company and also to ensure that the third parties distribute the products in line with Ukrainian local legislation and internal SOPs.

Requirements:

• Education: Higher pharmaceutical or chemical or biology education;
• Experience is minimum five years in the GMP field;
• Strong knowledge of Pharma legislation of Ukraine;
• Strong knowledge of the Ukrainain GxPs (GMP, GDP, GSP);
• English - proficiency is not a must, but will be an advantage;
• Advanced user of MS Office;
• Good communication, interpersonal, and influencing skills, good team player.

Company offers:

• Competitive remuneration and social package;
• Products of high quality;
• Work in professional team.
• You can send your detailed CV with photo to

☑ О компании:

Логотип (эмблема, торговая марка, бренд) компании:

Сфера деятельности компании: Медицина, фармацевтика, аптеки; Услуги для бизнеса; .

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