NITTO DENSEN KOGYO VIỆT NAM

Company Description

Danapha Pharmaceuticals is a leading pharmaceutical manufacturing and trading company in Vietnam. The company operates two GMP-WHO standard pharmaceutical factories for Eastern medicine and non-beta lactam drugs, along with a new GMP-EU standard factory under construction in the high-tech zone of Đà Nẵng. The work environment is friendly, with a professional work ethic that supports personal development.

Role Description

This is a full-time on-site role for a QA Manager - GMP_EU Factory at Danapha Pharmaceuticals located in Đà Nang. The QA Manager will be responsible for overseeing quality assurance activities in the GMP-EU factory, ensuring compliance with regulatory standards, and implementing quality control measures to maintain product quality and safety on a day-to-day basis.

Qualifications

• Quality Assurance, Regulatory Compliance, and Quality Control skills
• Knowledge of GMP-EU standards and pharmaceutical manufacturing processes
• Experience in conducting quality audits and inspections
• Strong attention to detail and analytical skills
• Excellent written and verbal communication skills
• Ability to work effectively in a team and cross-functional environment
• Bachelor's degree in Pharmacy, Chemistry, or related field
• Certifications in Quality Management or QA/QC would be beneficial