Sharareh Rezaei
Lewisburg,PA
Summary
Innovative and detail-oriented Chemical Engineering graduate student with extensive academic and industrial experience in pharmaceutical sciences and advanced material research. Skilled in designing and optimizing drug delivery systems and biomaterials, with expertise in cutting-edge analytical techniques such as HPLC, DLS, and TEM. Proven track record in quality assurance, formulation development, and process optimization, ensuring compliance with GMP and SOP standards. Adept at data analysis, problem-solving, and collaboration in interdisciplinary teams. Driven by a passion for advancing healthcare solutions through engineering, with a commitment to excellence and precision in both research and industry settings.
Overview
8
8
years of professional experience
Work History
Teaching Assistant
Bucknell University
08.2023 - Current
- Provided instructional support to faculty during laboratory and lecture sessions, ensuring smooth delivery of course material.
- Assisted students in understanding complex concepts, conducting experiments, and troubleshooting technical challenges in laboratory settings.
- Prepared laboratory setups, including equipment calibration and materials organization, to facilitate hands-on learning experiences.
- Evaluated student assignments, lab reports, and exams, offering constructive feedback to improve their understanding and performance.
- Maintained a safe and organized lab environment by enforcing safety protocols and ensuring compliance with university guidelines.
- Supported curriculum development by creating instructional materials and providing input on course design.
Research Assistant
Bucknell University
08.2023 - Current
- Designed and led research projects focusing on the stability and efficiency of liposome-based drug delivery carriers, optimizing their composition for enhanced performance.
- Strategically employed saturated (DMPC) and unsaturated (DOPC) lipids to evaluate their combined effects on liposome stability, degradation, and response to thermal stress.
- Utilized advanced analytical techniques including:
- DLS (Dynamic Light Scattering): For size distribution and stability assessments.
- HPLC (High-Performance Liquid Chromatography): For precise compositional analysis.
- Electron Microscopy (TEM and SEM): For structural imaging at nanoscale resolution.
- Developed experimental protocols to simulate diverse thermal conditions, uncovering degradation dynamics and lipid interactions under elevated temperatures.
- Generated reproducible data sets to support stability optimization, contributing to advancements in therapeutic delivery systems.
- Collaborated with faculty to enhance the uniformity and size of hydrogel beads for potential biomedical applications, focusing on improving processing techniques.
- Conducted solubility tests to determine optimal emulsion conditions for material preparation.
- Designed and tested filtration techniques to refine bead size and uniformity, identifying effective filter combinations for improved outcomes.
- Investigated the relationship between material properties and processing conditions, contributing to the broader understanding of hydrogel behavior.
- Prepared detailed reports and presented findings, showcasing advancements in material optimization for biomedical use.
R&D and QC Specialist
Niak Pharmaceutical Company
08.2019 - 06.2023
- Conducted chemical and physical analyses to ensure raw materials, intermediates, and finished products met stringent pharmacopoeia's standards (USP, BP, etc.).
- Performed stability testing of pharmaceutical products under various storage conditions, documenting results in compliance with GMP guidelines.
- Operated and maintained advanced laboratory equipment, including HPLC and UV-Vis spectrophotometers, ensuring accurate and reproducible results.
- Created and reviewed Standard Operating Procedures (SOPs) for laboratory practices to maintain regulatory compliance.
- Collaborated with production teams to address and resolve quality discrepancies during manufacturing processes.
- Monitored batch records to ensure traceability and compliance with quality standards.
- Developed and optimized formulations for new pharmaceutical products, focusing on improving efficacy, stability, and manufacturability.
- Conducted feasibility studies for new product development, evaluating the technical and regulatory requirements.
- Designed and performed experiments to analyze the stability and degradation patterns of formulations under varying conditions.
- Assessed the physicochemical properties of active pharmaceutical ingredients (APIs) and excipient for compatibility and performance.
- Prepared detailed reports and documentation for regulatory submissions and internal knowledge sharing.
- Worked collaboratively with cross-functional teams, including marketing and production, to ensure successful product launches.
Feasibility Study Specialist
Armin Moshaveran Company
03.2017 - 09.2021
- Followed all company policies and procedures to deliver quality work.
- Optimized customer experience by delivering superior services and effectively troubleshooting issues.
- Gathered, organized and input information into digital database.
- Improved customer satisfaction rates through proactive problem-solving and efficient complaint resolution.
- Conducted comprehensive feasibility assessments for diverse business ventures, including startups, expansions, and investment opportunities across various industries.
- Evaluated technical, operational, financial, and market factors to determine project viability and success potential.
- Developed detailed business models, cost-benefit analyses, and risk assessments to guide strategic decision-making.
- Collaborated with clients and stakeholders to gather requirements and provide tailored recommendations for project implementation.
- Prepared and presented feasibility reports outlining actionable insights, timelines, and resource allocation strategies to ensure informed decision-making.
Quality Assurance Technical Assistant
Paksaz Shimi Hirkan Company
06.2017 - 08.2019
- Supported the development, implementation, and maintenance of quality assurance systems to ensure compliance with industry regulations and standards.
- Assisted in preparing and reviewing technical documents, including SOPs, work instructions, and quality manuals, to align with organizational policies.
- Conducted audits and inspections of processes and products to identify non-conformities and recommend corrective actions.
- Coordinated with cross-functional teams to resolve quality issues and enhance process efficiency.
- Monitored quality metrics and prepared detailed reports to track progress and identify areas for continuous improvement.
- Provided technical support and training to staff on quality assurance processes and compliance requirements.
Education
Master of Science - Chemical Engineering
Bucknell University
Lewisburg, PA08-2025
Bachelor of Science - Chemical Engineering
Golestan University
Gorgan, Iran04-2018
Skills
- Analytical skills
- Data analysis
- HPLC (High-Performance Liquid Chromatography) for separation and quantification
- DLS (Dynamic Light Scattering) for particle size distribution
- TEM (Transmission Electron Microscopy) for high-resolution imaging
- Quality assurance and control
- Formulation development
- Stability testing
- GMP (Good Manufacturing Practices) compliance
- SOP (Standard Operating Procedures) documentation
- Process optimization
- Effective communication
Languages
Persian
Native or Bilingual
Turkish
Native or Bilingual
Spanish
Limited Working
English
Native or Bilingual
Timeline
Teaching Assistant
Bucknell University
08.2023 - Current
Research Assistant
Bucknell University
08.2023 - Current
R&D and QC Specialist
Niak Pharmaceutical Company
08.2019 - 06.2023
Quality Assurance Technical Assistant
Paksaz Shimi Hirkan Company
06.2017 - 08.2019
Feasibility Study Specialist
Armin Moshaveran Company
03.2017 - 09.2021
Master of Science - Chemical Engineering
Bucknell University
Bachelor of Science - Chemical Engineering
Golestan University
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