● Implement accreditation requirements including clean room, air generator, water generator, equipment, and drug production devices according to GMP principles.
● Prepare and report validation protocols, quality assurance of equipment, and validation of production processes.
● Identify potential quality risks in all processes and provide solutions to minimize them (based on risk management and process control).
● Plan, implement, and monitor the integration of operations and organizational processes.
● Analyze the results of quality control tests, provide feedback, and interpret the results to the relevant units.
Requirements
● Ability to direct and lead work teams.
● Proficient in analyzing problems and providing creative solutions.
● A persistent and serious person in achieving goals.
● Proficient in working with laboratory equipment and devices.
● Proficient in immunology, microbiology, and biochemistry.
● At least three years of work experience.