Thông tin tuyển dụng nhanh
Kinh nghiệm: Chưa có kinh nghiệm
Yêu cầu bằng cấp: Không yêu cầu
Số lượng cần tuyển: 0
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:
6F, 17 Ba Huyen Thanh Quan Str, Dist.3, HCMC
Hạn nộp hồ sơ: