Quality Coordinator

• Oct 2017 - Present

Business Development Manager

• Jun 2013 - Present

1- Identifies ideas by researching industry and related events, publications, and announcements; tracking individual contributors and their accomplishments.2- Locates or proposes potential business deals by contacting potential partners; discovering and exploring opportunities.3- Develops negotiating strategies and positions by studying integration of new venture with company strategies and operations; examining risks and potentials; estimating partners' needs and goals.4- Closes new business deals by coordinating requirements; developing and negotiating contracts; integrating contract requirements with business operations.5- Protects organization's value by keeping information confidential.6- Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.7- Enhances organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.

Quality Control & Quality Assurance inspector

• Oct 2011 - Oct 2017

Quality Control/Quality Assurance Duties and Skills Sample raw, packaging materials, labels, check containers for proper content label and of any shipping damage Measure packaging materials and record results, create or propose new packaging specifications Approve incoming materials, in-process production and finished products by confirming specifications, conduct visual inspection, measurement (weight variation, hardness, thickness, friability and disintegration tests) for tablets and capsules• Experience with chromatography analysis assays and method development/Validation techniques include specificity, linearity, limit of detection, quantization limit, accuracy and precision• Excellent knowledge of analytical, preparative and process HPLC, TLC, UV-Vis including the operation of other laboratory equipments, maintenance and trouble-shooting, Very good LC-MS knowledge and data interpretation Conduct various stability studies (forced degradation, pH, solubility and shelf-life) that complies with FDA/ICH regulations Reject and returning unacceptable materials, returning products for re-work, confirming re-work and communicating required adjustments to production supervisor Document inspection results by completing reports and logs, summarizing re-work and waste and input data into quality database using Enterprise Resource Planning (ERP) software Perform routine ATP swabbing test on multiple equipments and surfaces, also monitor temperature and humidity in warehouse and production area Report any out of specification (OoS) to the QC/QA manager for investigation and assist with corrective and preventive action (CAPA) Participate in internal audits prior to upcoming external audits  Maintain safe and healthy work environment by following standards and procedures that complies with legal regulations Write and review SOPs In addition to many other duties and responsibilities

Research Scientist

• Aug 2002 - Apr 2008

• Synthesized peptide analogs by solid or solution phase chemistry in a timely manner using a combination of manual and automated synthesizing methods, creating many potential cancer and cardiovascular drug candidates• Maintained and repaired instrumentation including automated peptide synthesizers, HPLC and lyophilizer saving approximately $40,000 in repair and maintenance costs• Excellent Mass Spectrometry (MS) data analysis and Interpretation (MALDI)• Used effective bargaining skills and efficient chemical inventory management to regularly save over 25% on chemical costs• Developed and optimized synthetic procedures maximizing the final yield percentage of the drug• Used HPLC and TLC to identify drug products and ensure purity• Performed protocols for stability studies and wrote reports complying with FDA regulations • Provided work-related training to new and existing employees, also trained some co-op students• Issued certificate of analysis (CoA) for drug substances and reviewed standard operating procedure (SOP)