Quality Assurance Specialist

Job description:

  • Participate in the process of building and developing documents in the quality system
  • Implement and distribute quality system documentation
  • Conduct internal training on the process system and guidelines of the Pharmaceutical Quality System
  • Participate in the change control process, change opinions within the scope of the Quality Assurance System
  • Participate and carry out internal inspection and “Gemba walk” at Davipharm to ensure the quality system and quality of products
  • Recognize and perform system activities (e.g., deviations, CAPA, change control, risk assessments) according to quality risk management and guidance. Digital registration and CAPA coordination
  • Coordinate corrective and preventive actions (CAPA) to ensure effective and timely implementation of established procedures, including initiation of actions to prevent non-compliance
  • Implement the discrepancies registration process to ensure effective and timely implementation according to the established process, using Problem Solving tools
  • Carry out the Change control number registration process, ensuring effective and timely implementation according to the implemented process
  • Implement quality projects to develop the Pharmaceutical Quality System at Davipharm
  • Participate in periodic Product Quality Reviews, including analyzing trends and determining appropriate actions
  • Implement and monitor quality process improvement indicators and ensure their implementation
  • Do other ad-hoc assignments from direct supervisor

Job requirement:

  • Pharmacist, Engineer, bachelor, intermediate pharmacist
  • Knowledge of pharmaceutical law, GMP requirements, manufacturing processes, testing process, validation
  • Knowledge of Pharmaceutical Quality system
  • Ability to perform risk assessment
  • 2 years of experience in pharmaceutical factory
  • Ability to analyze and solve problems.
  • Ability to work under high pressure and intensive deadlines
  • Understanding of systematic process of WHO GMP, EU GMP in the pharmaceutical industry.
  • MS Office 365: Microsoft Excel, Word
  • Meticulous, honest
  • Ability to interact with colleagues at all levels throughout the company
  • Good command of English skills

Please contact our Recruiter or apply via email recruitment@davipharm.info