LINH KIỆN ĐIỆN TỬ SEI

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 being built in the high-tech zone of Đà Nẵng. The work environment is friendly, with a professional work ethic that fosters personal development.

Role Description

This is a full-time on-site role for a QA Manager - GMP_EU Factory at Danapha Pharmaceuticals in Đà Nang. The QA Manager will be responsible for overseeing quality assurance activities, ensuring compliance with GMP-EU standards, managing quality control processes, conducting audits, and implementing quality improvement initiatives.

Qualifications

• Experience with GMP-EU standards and quality assurance in pharmaceutical manufacturing
• Knowledge of quality control processes and auditing procedures
• Strong problem-solving and decision-making skills
• Attention to detail and accuracy in documentation
• Excellent communication and leadership abilities
• Bachelor's degree in Pharmacy, Chemistry, or related field
• Quality Assurance certifications are a plus