Công Ty Cổ Phần Osr Việt Nam

Mô tả Công việc

• Revise and update Standard Operating Procedures (SOPs) related to assigned processes.
• Conduct training sessions on General Procedures (GPs) and specific processes for relevant staff.
• Perform regular risk assessments to identify and mitigate risks associated with assigned processes.
• Oversee product quality checks, blocking, releasing, and ensuring adherence to compliance standards.
• Follow up on Corrective and Preventive Actions (CAPA) to resolve quality-related issues.
• Control product master data, handle changes, and manage variations.
• Prepare and submit periodic reports for special controlled drugs as required by regulations.
• Maintain and ensure proper documentation related to Good Storage and Distribution Practices (GSDP).

Yêu Cầu Công Việc

Graduated from the University of Pharmacy

2 years of experience in a similar position.

Skilled in organizing work and problem solving, pharmacovigilance handling skills...