RD Analyst
- Thỏa thuận
- Toàn thời gian
Hạn nộp hồ sơ: 03/12/2026 (Còn 25 ngày)
Ứng tuyển sớm để được ưu tiên
Kết nối với Nhà tuyển dụng để tìm hiểu thông tin và gia tăng cơ hội trúng tuyển
Nhà tuyển dụng đang online
Company Description
Danapha Pharmaceutical JSC is a leading Vietnamese pharmaceutical company with over 60 years of experience in developing and manufacturing high-quality medicines. The company operates three manufacturing plants in which one is compliant with EU-GMP and a dedicated R&D center.
Role Description This full-time on-site RD Analyst role is based at Danapha Pharmaceuticals in Đà Nẵng. The RD Analyst will support research and development activities by designing and executing laboratory experiments, analyzing data, and contributing to the development and optimization of pharmaceutical formulations and processes.
Daily responsibilities include preparing and testing samples, documenting methods and results in accordance with regulatory and internal quality standards, and collaborating closely with scientists, production teams, and quality assurance. The role also involves participating in method validation, preparing technical reports, assisting with regulatory submissions, and helping implement new technologies or processes in line with EU-GMP and other relevant guidelines.
Qualifications
Strong analytical and laboratory skills, including experience with experimental design, data collection, and interpretation.
Knowledge of pharmaceutical R&D processes, formulation development, and method validation in compliance with EU-GMP or equivalent standards.
Familiarity with quality systems, documentation practices, and regulatory requirements relevant to pharmaceutical products.
Proficiency with common scientific and data analysis software; ability to prepare clear technical reports and presentations.
Bachelor's degree or higher in Pharmacy, Pharmaceutical Science, Chemistry, Biochemistry, or a related field.
Strong attention to detail, problem-solving abilities, and capacity to work accurately under time constraints.
Effective communication and teamwork skills, with the ability to collaborate across R&D, production, and quality functions.
Prior experience in a pharmaceutical R&D or QC/QA laboratory is an advantage; understanding of international markets is a plus.
Danapha Pharmaceutical JSC is a leading Vietnamese pharmaceutical company with over 60 years of experience in developing and manufacturing high-quality medicines. The company operates three manufacturing plants in which one is compliant with EU-GMP and a dedicated R&D center.
Role Description This full-time on-site RD Analyst role is based at Danapha Pharmaceuticals in Đà Nẵng. The RD Analyst will support research and development activities by designing and executing laboratory experiments, analyzing data, and contributing to the development and optimization of pharmaceutical formulations and processes.
Daily responsibilities include preparing and testing samples, documenting methods and results in accordance with regulatory and internal quality standards, and collaborating closely with scientists, production teams, and quality assurance. The role also involves participating in method validation, preparing technical reports, assisting with regulatory submissions, and helping implement new technologies or processes in line with EU-GMP and other relevant guidelines.
Qualifications
Strong analytical and laboratory skills, including experience with experimental design, data collection, and interpretation.
Knowledge of pharmaceutical R&D processes, formulation development, and method validation in compliance with EU-GMP or equivalent standards.
Familiarity with quality systems, documentation practices, and regulatory requirements relevant to pharmaceutical products.
Proficiency with common scientific and data analysis software; ability to prepare clear technical reports and presentations.
Bachelor's degree or higher in Pharmacy, Pharmaceutical Science, Chemistry, Biochemistry, or a related field.
Strong attention to detail, problem-solving abilities, and capacity to work accurately under time constraints.
Effective communication and teamwork skills, with the ability to collaborate across R&D, production, and quality functions.
Prior experience in a pharmaceutical R&D or QC/QA laboratory is an advantage; understanding of international markets is a plus.
Thông tin chung
- Thu nhập: Thỏa thuận
Việc làm tương tự khác
CÔNG TY CỔ PHẦN TẬP ĐOÀN FECON
Bắc Ninh, Đồng Nai, Tuyên Quang
20,000,000 - 28,000,000 VND
CÔNG TY CỔ PHẦN QUỐC TẾ NHẬT PHÁT TOKYO
Hồ Chí Minh
29.500 TWD/tháng
CÔNG TY CỔ PHẦN CÔNG NGHỆ TIÊU CHUẨN SINH HỌC VĨNH THỊNH VINHTHINH BIOSTADT JSC
Hồ Chí Minh
Từ 8 triệu - 10 triệu
CÔNG TY CỔ PHẦN GIÁO DỤC QUỐC TẾ IELTS ARENA
Hà Nội
18.000.000 - 25.000.000 VND
Công ty Cổ Phần Tin học Giải Pháp Tích Hợp Mở
Hồ Chí Minh
Thỏa thuân
Thông tin công việc
Vị trí:
Nhân viên
Hình thức làm việc:
Toàn thời gian
Việc làm tương tự
Cảnh báo dấu hiệu lừa đảo tuyển dụng
Đội ngũ hỗ trợ của JobOKO sẵn sàng đồng hành, tư vấn và giới thiệu những cơ hội việc làm phù hợp, giúp Ứng viên tự tin phát triển sự nghiệp và chinh phục mục tiêu nghề nghiệp bền vững.
Hotline CSKH
1900.63.63.84
Công ty Cổ phần JobOKO Toàn cầu
Đội ngũ hỗ trợ của JobOKO luôn chủ động tư vấn các giải pháp tuyển dụng tối ưu, cam kết đồng hành và hỗ trợ Quý Nhà tuyển dụng đạt được hiệu quả tuyển dụng bền vững.
Hotline CSKH
02473.068.388
Công ty Cổ phần JobOKO Toàn cầu