Pharma R&D Specialist (Work Location: VSIP 2 - Binh Duong)

Report occurrence of any deviation or technical problem within 24 hours of detection and recommend necessary measures to prevent occurrence of the same incident.
Ensure compliance to Good Documentation Practices (GDP). Ensure that documents are accurate, up- to- date, and truthful at all times.
Conduct field investigation to determine true root causes of issues, if applicable.
Develop analytical methods, formula for new products as assigned by Regional R&D- Technical Services Lead
Monitor and review stability test results in accordance with the validation study.
Other duties as may be assigned
Helping Regional team in timely preparing and implementing regulatory- compliant procedures for corrections and corrective actions of technical issues.
Prepare process validation procedures.
Prepare ACTD dossiers
Prepare process validation reports.
Maintain records of relevant data and information gathered and other documents required by GMP, and regulatory agencies.

Professional Background

Can speak and write in English.
University graduate, major in Pharmacy preferred.
At least 5 years of experience working as R&D researcher/analyst in developing new products. Familiar with equipment used in Production/Pilot.

Competency Requirements

Organizational capability
Strong cooperation/team work
Sense of initiative and creativity
Quality of work: can maintain high standards even in pressing deadlines.
Reliability (responsible, completes works in timely and consistent manner)
Self- management capability

Laptop, Chế độ bảo hiểm, Du Lịch, Phụ cấp, Xe đưa đón, Đồng phục, Chăm sóc sức khỏe, Đào tạo, Tăng lương, Công tác phí, Nghỉ phép năm

Cập nhật gần nhất lúc: 2025-09-19 05:00:03