This position monitors the overall Quality System status of the distribution center while ensuring compliance with drug, medical device, and local regulations
Job Summary
This position monitors the overall Quality System status of the distribution center while ensuring compliance with drug, medical device, and local regulations.
The role involves writing and revising Standard Operating Procedures, conducting regular facility inspections, and coordinating corrective actions to maintain quality processes.
Candidates will liaise with TFDA officials during regulatory audits and assist in developing proactive strategies to prevent future system or process problems.
Matching Summary
This position monitors the overall Quality System status of the distribution center while ensuring compliance with drug, medical device, and local regulations.
Skills & Requirements
Must-have
GMP training for staff
Standard Operating Procedure writing
Facility inspection and reporting
Nice-to-have
Proactive strategy development
Client communication skills
Continuous improvement mindset
Key Requirements
Bachelor's Degree in Science related field
Pharmaceutical or medical device industry experience preferred