Вакансия № 11710111 на должность "Quality assurance&Quality control Manager/Менеджер службы контроля качества (Elets)" в городе (регионе) Липецк, Россия от компании "Syngenta" на сайте Электронный Центр Занятости Населения
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Организация работает в следующих сферах деятельности: Сельское хозяйство; .
Репутация компании "Syngenta" в отзывах работников:
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Обязательное требование к опыту работы искомого сотрудника: 3–6 лет.
График работы: полный день.
Тип занятости: полная занятость.
Вакансия № 11710111 добавлена в базу данных: Пятница, 29 марта 2024 года.
Дата обновления этого объявления: Вторник, 23 апреля 2024 года.
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Работодатель предложит заработную плату по результатам собеседования с соискателем работы.
Dear candidates,
This vacancy is opened in Elets. We are ready to discuss the possibility of relocation.
Role Purpose
QA: Monitor and advise on the performance of Syngenta QMS, applying Syngenta Quality Policy through all manufacturing activities in order to meet product standards and customer satisfaction required. Provide technical expertise and define Quality procedures, based on Syngenta Quality Codes of Practice.
QC: Ensure the correct application of the Quality Control Plan in site activities, including full implementation of QCoP 005 (Residual Impurity Management), based on Syngenta QMS Standards and Territory/ Regional/ Global regulatory requirements. Manage on site / off site Quality laboratory staff and activities.
Accountabilities
QC Mgr:
- Organize and plan lab activities and resources according to the production workload
- Ensure repeatability and reliability of lab results
- Implement and maintain the relevant accreditation of the lab and quality procedures.
- Ensure appropriate KPI reporting of agreed quality metrics, system records are updated and timely reporting of any quality incidents
- Recruitment and management of laboratory staff using Syngenta individual Performance management and definition of individual training needs and plans
- Identification of training needs
- Ensure that Syngenta Quality policies and standards are followed
- Budget responsibility for laboratory and associated quality cost centres on site
- As a member of the site leadership team, proactively contribute to the development and implementation of site strategy
QA Mgr:
- Referring to Global and Local Quality Standard to develop Quality Policy and Standard for Implementing consistently in the site
- Ensuring the development and implementation of the annual quality plan, strategies, objectives in compliance with QMS
- Ensuring the development of specifications for packaging, leading its quality improvement projects, participating in developing new packaging initiatives together with Marketing and Purchasing functions.
- Dealing with Government officer and Global Quality Function related to Quality to ensure that all activities is being compliance with local registration.
- Handle the supplier & customer complaints; follow up the corrective / preventive action of the non conformity.
- Organize and monitor supervision in NC, Customer complaint investigation process to ensure that rood causes is verified and corrective and preventive input action to avoid of recurrence.
- Meeting Company Quality Manual / Objectives
- As a member of the site leadership team, proactively contribute to the development and implementation of site strategy.
Knowledge & Experience
- Quality Management professional with + 5 years’ experience in the implementation of quality and continuous improvement across a sizeable manufacturing organization, with line management experience.
- Experience in a chemical or pharmaceutical manufacturing environment is essential.
- Analytical laboratory experience with in-depth knowledge of QC processes.
We offer:
- A competitive salary/compensation and bonus opportunities;
- Voluntary medical insurance, life insurance;
- Meal allowance;
- Regular professional trainings;
- Extended paid vacation, employee assistance program.
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