Quality Project Manager
Вакансия № 27660839 в населенном пункте (городе) Алматы, Казахстан от компании "Johnson & Johnson" на сайте Мультирегиональный Электронный Центр Занятости Населения (ЦЗН).
Уважаемый соискатель вакансий, Вы можете перейти на сайт прямого работодателя "Johnson & Johnson" для ознакомления с информацией о компании (фирме, организации, ИП). Смотрите Веб-сайт "Johnson & Johnson" - http://www.jnjru.ru
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Организация работает в следующих сферах деятельности: Промышленное оборудование, техника, станки и комплектующие; Товары народного потребления (непищевые); Медицина, фармацевтика, аптеки; .
Репутация компании "Johnson & Johnson" 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 № 27660839 добавлена в базу данных: Понедельник, 8 апреля 2024 года.
Дата обновления этого объявления: Среда, 1 мая 2024 года.
| Рейтинг вакансии: 10,4 из 100 баллов |
Работодатель предложит заработную плату по результатам собеседования с соискателем работы.
Janssen as a part of Johnson & Johnson Family of Companies is looking for a strong candidate for a Quality Project Manager located in Almaty.
You’ll lead provision of consulting, informational and other support for the creation and roll-out of a quality system at a pharmaceutical warehouse, which will be operated by a legal entity that will be created by a company of the Johnson & Johnson group for purposes of wholesale of medicines in Kazakhstan (“Newco”) in line with the regulations of Kazakhstan and J&J policies, standards and procedures.
YOUR responsibilities & YOUR impact:
- Consulting support on development and implementation on the following:
- Development and roll-out of a quality management system at the Warehouse;
- Development of the quality management and oversight of supplier (3PL);
- Development of the optimal schedule for preparing & implementation required quality framework and quality management system for all 3PL activities (assembling, packing, storing, inspecting, labeling and delivering finished goods to customers);
- Preparation of the necessary documentation and requirements for quality management systems in accordance with the legislation of the Republic of Kazakhstan and company standards;
- Development of controls and quality standards for all distribution and inventory management activities (e.g. receiving, pick, pack, lot reconciliation);
- Development of requirements for repackaging and relabelling operations, temperature control;
- The appropriate handling of distribution related customer complaints (Delivery Service Issues) including track and trend and mitigation of Quality related issues;
- Discussion and alignment of the suggested schedule and step-plan of preparation of the Warehouse with other members of the project team;
- Control over compliance with the requirements of the legislation of the Republic of Kazakhstan in the field of circulation of medicines at all stages of preparation of the Warehouse for operation;
- Control over compliance at the Warehouse with Good Practices (GDP) in the field of quality.
We would love to hear from YOU, if you have:
- Diverse business background, preferably with direct experience in Pharm segment, with specific quality, regulatory and regulatory compliance competencies in the areas of: customer service, distribution and commercial customer interface. Experience in positions of increasing responsibility, with broadly based quality management experience;
- Proven success in DC Q&C management with customer and business focus;
- Quality improvement programs, risk reduction projects, supply chain added value solutions;
- Understanding the linkages in quality and regulatory compliance in delivery to customer and health authority;
- Compliance experience, QMS experience;
- Change management and project management experience, strong presentation skills, issue remediation experience, collaborative approach, managing complexity;
- Analytical skills with a Bifocal approach - ability to zoom-in/zoom-out for tactical, high-level and detailed, etc.;
- Previous experience interfacing with global regulatory agencies, e.g., FDA, EMA, MHRA, TGA, notified bodies, etc, and a history of success and credibility resolving complex regulatory compliance issues;
- Master degree in engineering, pharmacy, scientific, business disciplines. Will accept the equivalent relevant industry experience if no degree;
- Organized, and able to leadwork effectively with people within a complex social, cultural and political environment;
- Must have excellent communication skills, able to inspire trust and quickly build credibility within the Quality & Compliance, Supply Chain, and Commercial organizations;
- Must have strong collaboration and influence management skills to partner effectively across functions and operating units;
- “Hands-on” operational orientation;
- Accountability, with a strong desire to commit, be held accountable and be rewarded for delivering results. Recognizes and builds support for change. Engages in constructive conflict;
- Ability to fit in well culturally in a complex organization.
This is what awaits YOU at J&J:
- An opportunity to be part of a global market leader;
- A dynamic and inspiring working environment;
- Many opportunities to work on challenging projects and assignments;
- Possibilities for further personal as well as professional development;
- Many employees benefit.
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