Mô tả công việc
Mô tả Công việc
1. Compliance Implementation
Implement assigned compliance activities to ensure adherence to applicable standards.
Follow established procedures to support compliance with Good Practices (e.g., GLP, GMP).
Ensure data integrity (ALCOA+) principles are applied in daily R&D activities.
Keep updated with relevant regulatory requirements and internal procedures.
2. Change Control & Risk Assessment
Support to ensure proper documentation and timely submission for change control process.
Participate in risk assessments related to product development and process changes as assigned.
Assist in the investigation and documentation of deviations and non-conformances.
3. Documentation & Process Support
Prepare, review, and maintain R&D documentation to ensure compliance with good practices provisions.
Support process harmonization activities by following standardized procedures and templates.
4. Cross-functional Coordination
Coordinate with internal teams including Formulation Development, QA, QC, RA, and other departments for compliance-related activities.
Support communication and alignment of R&D documentation and requirements across functions.
5. Technical & Operational Support
Provide support during product registration, validation, and troubleshooting activities when required.
Participate in analytical method development or related laboratory activities as assigned.
6. Audit & Inspection Support
Support internal and external audits by preparing required documents and records.
Assist in tracking and following up audit findings and CAPA actions.
7. Equipment & GLP Compliance
Ensure proper use and maintenance of R&D equipment in accordance with GLP provisions
Maintain accurate and complete records related to equipment usage.
8. Training and Awareness
Conduct regular training sessions for staff on compliance management practices.
Promote a quality culture within the R&D department.
Yêu cầu
Yêu Cầu Công Việc
Official Education: Bachelor's degree or master's degree - Major should be related to pharmacy or organic chemistry
Work/ Skills/ Experiences
1-2 years in the quality field is preferred
Have good attention to detail and ability to thoroughly cross check self and others.
Have a structured and organised approach to document and record management.
Basic knowledge of regulatory requirements and industry standards.
Good attention to detail and organizational skills.
Effective communication and interpersonal skills.
Ability to work independently and as part of a team.
Good organizational and time management skills with the ability to prioritize and manage multiple projects and deadlines.
Flexibility to adapt to frequent project changes.
Supplementary Certificate
Proficient in MS Office (Word, Excel, PowerPoint)
Good command of English (speaking, reading, writing); TOEIC, etc
Quyền lợi
Chế độ bảo hiểm
Du Lịch
Phụ cấp
Xe đưa đón
Đồng phục
Chế độ thưởng
Chăm sóc sức khỏe
Đào tạo
Tăng lương
Nghỉ phép năm
CLB thể thao
Thông tin chung
Nơi làm việc
- 16 VSIP, Street 5, Vietnam-Singapore Industrial Park
Cách thức ứng tuyển
Ứng viên nộp hồ sơ trực tuyến bằng cách bấm nút Ứng tuyển bên dưới:
Hạn nộp: 04/06/2026
Rohto Pharmaceutical Co., Ltd là một trong những Tập đoàn Dược phẩm hàng đầu của Nhật Bản chuyên về các sản phẩm chăm sóc sức khoẻ và sắc đẹp với các sản phẩm nổi tiếng như Thuốc nhỏ mắt V.Rohto, Sunplay, Hada Labo, Selsun, Lipice, Lip On Lip, Remos, Blossomy, Acnes...Được ra đời năm 1899 và hiện đã có nhà máy tại nhiều quốc gia trên khắp châu lục, Rohto ngày càng khẳng định được vị thế của mình trong lòng người tiêu dùng trên khắp thế giới.
Tiếp nối sự phát triển của tập đoàn,...
Quy mô công ty
Từ 501 - 1000 nhân viên
