Management representative for the company’s quality program (ISO 9001, ISO 22000, FSSC 22000 V5.1, cGMP, Non-GMO, Halal, Kosher) in two locations.Develop, implement and update company administrative control procedures and department procedures to maintain compliance with company certifications or regulatory requirements (ISO 9001, ISO 22000, FSSC 22000, cGMP, Non-GMO).Implementation of certified Quality Management Software (QT9).Perform internal audits and vendor audits to ensure compliance to company, customer and regulatory requirements.Train company personnel on quality/safety programs, FDA Good Manufacturing Practices, and Food Defense Plan.Monitor CAPA and NCP completion and evaluation of effectiveness of root cause analysis and implemented corrective actions.

Establish, document and maintain Company's Quality Management SystemConduct QMS, GMP and HACCP trainings.Provide QMS and GMP training material to management.Ensure compliance with the GMP requirements for Disease Control, Cleanliness, Education and Training of personnel.Independently review QMS suitability and effectiveness.Independently plan and conduct internal and external audits / assessments and report results to management.

Chemical, physical and bacteriological analysis on manufacture samples, third party samples and company's finished products. Data analysis, laboratory safety and management and disposal of chemicals.

Consultant, architecture, develop and implementation of products. Development of biomedical devices.

Architecture, develop and implement products. Creating noninvasive glucose meter and project management.

Basic computer teaching to elderly people.

Software and hardware repair.