Chi tiết tuyển dụng

Tuyển dụng Analytical Development Manager

Địa điểm tuyển dụng: Đồng Nai
Mức lương: Thỏa thuận
Tin xác thực Lượt xem: 184

Thông tin tuyển dụng nhanh

Kinh nghiệm: Chưa có kinh nghiệm

Yêu cầu bằng cấp: Không yêu cầu

Số lượng cần tuyển: 0

Ngành nghề:

Hình thức làm việc: Toàn thời gian cố định

Chức vụ: Thực tập sinh

Yêu cầu giới tính: Không yêu cầu

Mô tả công việc

Belonging to Research, Development & Licensing (RDL) Asia Department and reporting directly to Pharmaceutical Development Manager, this position will have the following key mission:
 To manage and plan the internal or external Analytical Studies to ensure the follow-up of studies within the required time limits and according to allocated budgets
 To propose an analytic strategy, from Evaluation up to Registration phase, adapted to the targeting countries (different for HQ or local projects), taking into account need of reagents, standards, equipment…
 To lead and monitor the writing part II for registration dossier
 To participate in working groups (investigations) with Head Quarter and other Virbac R&D affiliates if needed
 To monitor technical product compliance
 To perform the transfer of technical documents to factory and / or other laboratories
 To manage the personnel and organization of Analytical laboratory, ensuring the achievement of qualitative and quantitative goals of the laboratory through the performance of team
 To manage the budget of Analytical laboratory.

Quyền lợi được hưởng

- 13th month salary, Annual Bonus; possible training in France
- Health Insurance Gras Savoye; Interaction with foreigners, prove Vietnamese talent
- Shuttle bus; special benefits for managerial level

Yêu cầu công việc

 Bachelor of Master of Chemistry/ Pharmacy or scientific degree with strong chemistry content
 Minimum of 3 years’ experience in the similar positions at multinational companies
 Good knowledge/experience of analytical technique, instrumentation and qualification procedures in pharmaceuticals ingredients/ products qualification and quantification methods
 Strong experience of working in a cGMP/GLP environment. Having knowledge of ICH guidelines and pharmacopoeia requirements
 General knowledge of the pharmaceutical drug development process.
 Strong experience of method development, method validation and method transfer requirements.
 Good understanding of statistical tools in applied analytical chemistry
 Proven leadership skill and strong personal skills
 Good at English & IT skills (data processing software…)
 Ability to work under pressure, teamwork, determined.
 Working place: Song May IZ, Trang Bom, Dongnai.
We will contact the suitable candidates.

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Thông tin liên hệ

Người liên hệ:

Địa chỉ: 6F, 17 Ba Huyen Thanh Quan Str, Dist.3, HCMC

Hạn nộp hồ sơ: 03/04/2019

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