Medication Support Liaison

• Jun 2023 - Present

Pharma Consultant

• Jan 2020 - Mar 2023

1. Providing medical information to pharmaceutical companies regarding new drugs 2. Evaluating the safety and efficacy of new drug formulations to ensure they meet regulatory standards 3. Develop strategies to educate consumers about new medications to ensure they are used safely and effectively 4. Recommending regulatory changes to improve the efficiency of drug manufacturing processes 5. Develop and maximize social marketing strategies based on Monitoring and Evaluation findings 6. Makes sound recommendations to improve productivity, solutions to issues affecting quality, and health and safety. 7. Provide monitoring and evaluation team with regular recommendations/inputs on quality control assessments 8. Monitors and evaluates selling points on regular basis and provide the technical team with the recommendation 9. Ensures compliance with importation, distribution, and stock management, equipment, Show less

Process Engineer

• Jan 2018 - Dec 2019

 Hand on support manufacturing and troubleshooting in machine bottelpack 364 and process enhancement activities.  Lead and conduct Shop Floor Meting (SFM) with HOD’s, Engineers, Technicians and Line leaders.  Will monitor and verify the Hygiene Program activities.  Manage equipment vendors to resolve technical issues and perform calibration for each machine.  Participate in Project Reduce Rework in filling area.  Complete key in and reviewing the Batch Manufacturing Record for each batch. Show less

Quality Assurance

• Apr 2017 - Oct 2017

 Performing In-Process QA activities primarily routine in-process checks, line clearance and etc. for Drug Product and Drug Substance facility. Online reviewing of Drug Product and Drug Substance batch records and monitoring of Drug substance manufacturing activities. Involving in investigations related to QA and Production activities and implementation of CAPA as per the investigation outcomes. Prepared QMS related documents to continuing improve test method by revising related SOP. Adhered to Good laboratory practice (GLP), Good documentation practice (GDP) and Current goods manufacturing practice (cGMP As expertise in microbiology and In- Process involved in various internal and major external audits such as FDA, EMA and NPRA. Show less

Quality Control Microbiologist

• Dec 2015 - Apr 2017

 Performed receiving of microbiological sample, performed subculture and isolates identification using VITEK 2 Compact. Performed Gram staining, fungal staining, biochemical test and any other quality control test. Interpretation of microbiological result, prepared test report and prepared trending data of microbial isolates which obtained from Environmental monitoring, water and product sample. Performed microbial isolates preservation using cryobeads and created isolates library. Expert in handling equipment related to microbiological identification process such as VITEK 2 Compact, Microscope, Stereoscopic zoom microscope, Biological safety cabinet, incubator and autoclave. Successfully accomplished various investigations by involving identifying microbiological contamination in media fill failure, OOS and OOT. Show less

QA Analyst

• Dec 2015 - Apr 2017