Thực tập sinh Đăng ký sản phẩm (Regulatory Affairs Intern)Công Ty TNHH Qualtech Consulting Corporation
Nơi làm việc: Hồ Chí Minh
Ngành nghề: Y tế - Dược, Thực tập, Hành chính - Văn phòng, Hóa học - Sinh học, Chăm sóc sức khỏe, Hóa học / Sinh học / Thực phẩm / Môi trường, Pháp luật/ Pháp lý
Lương: 4 - 9 triệu VNĐ
Hình thức: Thực tập
Ngày đăng: 12/07/2024
Hạn nộp: 11/08/2024
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Mô tả công việc
Introduction
Qualtech is an Asia Medical Device Consulting and Clinical Trial (CRO) Company with branch offices in China, Hong Kong, Indonesia, Japan, Malaysia, Philippines, Singapore, Vietnam, Thailand, Korea, USA and Germany. We are looking for a Talented Regulatory Affairs Intern who is fluent in English and be able to understand to medical device regulations in the countries we service for. Qualtech is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people.
Job description
Oversight of regulatory submissions for assigned projects/countries, which may include completion of submissions or notifications, as required.
Ability to read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
Investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.
Other duties as assigned.
Qualtech is an Asia Medical Device Consulting and Clinical Trial (CRO) Company with branch offices in China, Hong Kong, Indonesia, Japan, Malaysia, Philippines, Singapore, Vietnam, Thailand, Korea, USA and Germany. We are looking for a Talented Regulatory Affairs Intern who is fluent in English and be able to understand to medical device regulations in the countries we service for. Qualtech is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people.
Job description
Oversight of regulatory submissions for assigned projects/countries, which may include completion of submissions or notifications, as required.
Ability to read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
Investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.
Other duties as assigned.
Yêu cầu công việc
Requirements
Can workat least 24hours per weekfor a duration of4to 6 months.
Fresh graduates for senior students in related majors, such as biomedical engineering, biotechnology and medicinal chemistry
Fluent in Englishis a must, in other languages will be an advantage. Candidates who can speak Chinese will be a big plus.
Ability to manage multiple projects, set priorities to meet deadlines.
Keeping attention to details.
Strong interpersonal skills, both written and oral.
Basic skills in MS Office: Word, PowerPoint, Excel, Outlook.
Only recruiting female candidates.
Can workat least 24hours per weekfor a duration of4to 6 months.
Fresh graduates for senior students in related majors, such as biomedical engineering, biotechnology and medicinal chemistry
Fluent in Englishis a must, in other languages will be an advantage. Candidates who can speak Chinese will be a big plus.
Ability to manage multiple projects, set priorities to meet deadlines.
Keeping attention to details.
Strong interpersonal skills, both written and oral.
Basic skills in MS Office: Word, PowerPoint, Excel, Outlook.
Only recruiting female candidates.
Quyền lợi được hưởng
Benefits
Allowance:Thehourly rateranges fromVND 40,000 to 50,000, depending on ability.
Confirmation of completing the internship.
Have chances to become a full-time employee.
Professional, dynamic working environment.
Allowance:Thehourly rateranges fromVND 40,000 to 50,000, depending on ability.
Confirmation of completing the internship.
Have chances to become a full-time employee.
Professional, dynamic working environment.
Giới thiệu công ty
Công Ty TNHH Qualtech Consulting Corporation việc làm
11Bis Phan Ngữ, Phường Đa Kao, Quận 1, Thành phố Hồ Chí Minh, Việt Nam
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Vị trí Thực tập sinh Đăng ký sản phẩm (Regulatory Affairs Intern) do công ty Công Ty TNHH Qualtech Consulting Corporation tuyển dụng tại Hồ Chí Minh, Joboko tự động tổng hợp mức lương 4 - 9 triệu VNĐ, tìm thêm việc làm về Thực tập sinh Đăng ký sản phẩm (Regulatory Affairs Intern) hoặc công ty Công Ty TNHH Qualtech Consulting Corporation ở các link phía trên
Giới thiệu công ty
Công Ty TNHH Qualtech Consulting Corporation việc làm
11Bis Phan Ngữ, Phường Đa Kao, Quận 1, Thành phố Hồ Chí Minh, Việt Nam