Being a representative of company in connection with external parties and develop organization strategy in quality aspects. Manage both commercial and distribution quality functions- for examples product release, change control, deviation management and validation- to support sales and marketing, distribution and clients business. Ensure that operations are in compliance with international standards- including ISO9001, ISO13485, Good Distribution Practice(GDP), Good Manufacturing Practice(GMP) for secondary packaging and Good Clinical Practice(GCP)- local law and regulation and clients specific requirements. Provide guidance to teams enhancing their understanding in pharmaceutical quality system and technical requirement allowing self continuous improvement.

Ensure that operations are in compliance with international standards- including ISO9001, ISO13485, Good Distribution Practice(GDP), Good Manufacturing Practice(GMP) for secondary packaging and Good Clinical Practice(GCP)- local law and regulation and clients specific requirements. Provide guidance to teams enhancing their understanding in pharmaceutical quality system and technical requirement allowing self continuous improvement.

Manage resources, human and monetary, of production department ensuring products supplied to market as planner in term of quality, quantity and cost covering 2 large volume parenterals(LVP) and 2 medicinal food manufacturing plants.Direct 2 IV solution manufacturing plant and 2 medical food manufacturing plant

Maneuver Quality Control(QC) and Quality Assurance(QA) team expertise assuring quality of products manufacture by own facility and contract manufacturer. Acquire additional technological advancement into QC department in preparation for new product development and introduction.

Govern company quality system- including document control, deviation management and etc.- and also working with external GMP expert to deploy quality improvement initiation. Lead quality system integration during business acquisition.

●Established Faculty of Pharmaceutical Science, Burapha University during May-Dec 2010 acting as Deputy Dean on planning and quality assurance affairs.●Set up 2 drugstores for pharmacy student practice.●Set up sterile product dosage form manufacturing course.●Working with Thai FDA for PIC/S GMP guideline implementation.

Leveraged operation knowledge to QC staffs in preparation for Quality Assurance function setup.

Oversaw solid dosage form manufacturing division. Improved tablet production productivity for 2 times.

Created SOP and Master Batch Record of newly established manufacturing facility.