Job summary

Job Responsibilities

• Certification and releasing finished products to the market

• Organization, implementation and improvement of the Pharmaceutical Quality System. Controls and assessment of the functioning of the quality system

• Initiating and coordinating corrective and preventive actions. Coordination of deviations and complaints process and supervision of CAPA activities in order to eliminate negative events

• Establishing indicators for the improvement of quality processes and ensuring their implementation and preparation of report according to procedures.

• Implementation and care for the use of Problem Solving tools

• Full integration of the quality system in cooperation with the Production Department in production area with other areas of the company

• Coordination of activities leading to compliance with GMP requirements

• Coordination of activities related to the availability of products in accordance with the objectives

• Supervision of the process of developing, reviewing and approving documentation in quality system

• Performing internal trainings (as a trainer) of procedures/ instructions/ amendments system to quality documents and guidelines of the Pharmaceutical Quality System

• Team management in terms of achieving business goals, team development, prioritizing, recruiting

• Participation in the investigation of complaints, ensuring their efficient and timely implementation in accordance with the implemented procedure.

• Do other ad-hoc assignments from direct supervisor.

Experience requirements

• Pharmcist, Engineer, bachelor, intermediate pharmacist

• At least 3 years of experience in QA department

• Knowledge of pharmaceutical law, GMP requirements, manufacturing processes, testing process, validation.

• Excellent knowledge of the implementation of Pharmaceutical Quality system.

• 2-3 years of experience in pharmaceutical factory (operational area).

• Ability to analyze and solve problems.

• Ability to work under high pressure and intensive deadlines.

• Understand the systematic process of WHO GMP, EU GMP in the pharmaceutical industry.

• MS Office 365: Microsoft Excel, Word, Auto cad

• Good command of English skills.

Education requirements

• Pharmcist, Engineer, bachelor, intermediate pharmacist

If you are keen on the role, please directly contact Ms. Khanh Vy via Zalo: 0908 609 952 or email: khanhvy.nguyen@adecco.com

Contact Person

• Khanh Vy Nguyen
• Adecco
• Tel.