• Represent the full range of Manufacturing and Quality capabilities to customers with Softgels, VeggieSoft Softgels, Gummies, Tablets, Capsules, Powders, probiotics and Liquids dosage forms.• Support the Business Development Managers in providing quick answers and problem-solving for formulation and manufacturing issues• Provide industry intelligence to assist the company to improve product offerings and services

• Design formulations and test plans, develop manufacturing process, and prepare stability batches for confections, semi solid and liquid products.• Ensure seamless technology transfer of processes between pilot plants and into final commercial manufacturing plants.• Design and optimize various formulation and filling unit operations including active ingredients dissolution of dispersion, mixing, emulsification, and bottle/tube filling.•Evaluate research to maintain and improve lines. • Develop project plans, coordinate projects and manage projects team activities; develop workable implementation plans, monitor transition and evaluate results.• Evaluate relevant characteristics of raw materials and experimental batches to develop robust manufacturing practices• Provide technical support to the organization, including Quality, Regulatory, Product Development, Product, Brand, Customer service and sales team by answer questions and providing supporting documents. • Responsibilities include qualifying new raw materials (excipients and APls), recommending specifications for products and designing and evaluating product manufacturing processes using quality by design principles for materials and process parameters evaluation and qualification.• Responsible for formulation and reformulation efforts. • Generate, distribute and implement knowledge about raw materials, formulations and manufacturing process.

• Prepare samples and conducting instrumental analyses (HPLC, GC, LC-MS, etc.) in the analytical laboratory; experience working and extracting API from different biological matrices. • Design formulations and test plans, develop manufacturing process, and prepare stability and clinical batches for solid, semi solid and liquid products. • Ensure seamless technology transfer of processes between pilot plants and into final commercial manufacturing plants. • Design and optimize various formulation and filling unit operations including active ingredients dissolution of dispersion, mixing, emulsification, and bottle/tube filling. • Experienced in granulation (fluidized bed coater, spray dryer, pan coater, extrusion), milling and microencapsulation ( extrusion, fluidized bed, spray drying)• Develop project plans, coordinate projects and manage projects team activities; develop workable implementation plans, monitor transition and evaluate results. • Evaluate relevant characteristics of raw materials and experimental batches to develop robust manufacturing practices• Working knowledge of experimental designs and clinical manufacturing, validation. and report writing for regulatory submissions.• Proficient with interpreting and implementing cGMPs, cGLPs, ICH, USP, FDA, DEA and OSHA guidelines.• Experience in product lifecycle - Product and process development, clinical trials. validation and regulatory submissions, commercial GMP manufacturing• Responsibilities include qualifying new raw materials (excipients and APls), recommending specifications for products and designing and evaluating product manufacturing processes using quality by design principles for materials and process parameters evaluation and qualification.• Leading the formulation optimization and scale up studies based on in-depth understanding of manufacturing processes for solid, semi-solid and liquid dosage forms

• Work closely with Formulation and Analytical team to develop liquid, semi solid, solid or confectionary dosage (gummies) prototypes. • Pre-formulation and formulation studies of gummies, scale up and transfer to manufacturing. • Prepare samples and conducting instrumental analyses (HPLC, GC, LC-MS, etc.) in the analytical laboratory on macro and trace Vitamins and minerals; experience working and extracting API from different biological matrices. • Maintain and apply current knowledge of cGMP documents and guidance, other FDA/ICH guidance and SOPs.• Help method development for Centrum Clusivol (liquid Centrum) analytical assay. • Works in the lab making prototype scale batches using manufacturing equipment including, but not limited to blenders, tablet presses, coating pans. Preparation of GMP batches• Proficient in tablet physical characterization tests (hardness, Friability, DT, Color Quest); powder flow characterization test (Ring Shear Cell Tester, Flodex, Bulk and Tapped Density); particles size analysis (Sonic Sifter, QicPic, Rotap). • Experienced in granulation (fluidized bed coater, spray dryer, pan coater, extrusion), milling (hammer mill, pin mill).• Experience in powder processing technologies such as mixing, high shear and fluid bed wet granulation, spray drying roller compaction.• Experience in emulsion/suspension (homogenizer, polymerization)• Communicating data and conclusions in clear oral and written reports.• Transferring process knowledge to and conducting scale-up experiments at manufacturing sites.• Support the development, validation and transfer of analytical methods in support of API and/or drug product manufacture and/or stand-alone analytical projects.• Help design and actively participated in consumer studies.• Experience in tech transfers

• Subject expert in microscopy techniques. • Understood the mechanisms involved in the transduction of salty and sour taste at the receptor level in the taste receptor cells. • Thorough understanding the science/principle of Cellular Regulation of Salt Taste Transduction

Understood the electrical activity of the heart at the cell, membrane, and channel level.• Investigated the mechanisms on the regulation of mechanosensitive and volume-sensitive ion channels in cardiac myocytes.• Redox regulation of lipid raft formulation in coronary arterial endothelial cells.• NADPH oxidase-associated electron currents and superoxide production in single coronary arterial smooth muscle cells.

• Prevent, diagnose and treat conditions of the cardiovascular system• Performed limited invasive procedures, such as cardiac catheterizations, defibrillator implants and pacemaker insertion.• Investigated protective effective of Tetrandrine on experimental myocardial ischemia and reperfusion injury