Sundae Morant Email & Phone Number

Baltimore, Maryland, United States

Expertly analyze metabolic activity of human and animal cells utilizing advanced HPLC and LCMS techniques, enhancing understanding of biochemical processes.Develop and validate analytical methods tailored to client specifications, resulting in improved testing accuracy and efficiency.Oversee laboratory equipment maintenance, troubleshooting malfunctions and ensuring optimal operational readiness.Conduct comprehensive evaluations of chromatographic data, ensuring adherence to method parameters and quality standards.Uphold strict compliance with laboratory health and safety regulations, fostering a safe work environment.Implement effective tracking systems for testing schedules, significantly increasing laboratory throughput.Compile and report analytical data using Microsoft Excel, contributing to data integrity and actionable insights.

Piscataway, New Jersey, United States

✔ Analyze organic & inorganic compounds to determine their composition.✔ Conduct qualitative and quantitative experiments taking into account the volume and structure of ingredients.✔ Customize formulas and use different reagents to test chemical reactions.✔ Write technical reports of the test results.✔ Develop nonstandard tests for chemical products.✔ Maintain lab equipment and troubleshoot or report on malfunctions.✔ Refine chemical products to improve their quality.✔ Ensure compliance with laboratory health and safety guidelines.✔ Sterilize equipment and store materials in secure places.✔ Daily login and tracking of inhouse & subcontracting sample submission and distribution of samples to be analyzed.✔ Analyzed cleaning validation swab samples, using TOC instrumentation.✔ Coordinate Testing of OTC Imports, and creation of CofA’s.

Gaithersburg, Maryland, United States

✔ Formulate product prototypes, evaluate them for chemical and physical properties, performance, and stability.✔ Research product formulations and properties of raw materials.✔ Support scale-ups from prototype to commercial manufacture particularly to Good Manufacturing Practices (GMPs).✔ Obtain process technology and equipment information for production.✔ Support on technical service for operations and consumer relations.✔ Conduct research and field evaluations on new products.✔ Develop new products and improve the functioning of existing products.✔ Analyzed samples using HPLC, Viscometer, pH meter, Conductivity.✔ Conduct experimental trials on new materials and processes.✔ Determine the best processing conditions for producing experimental samples.✔ Devise prototype membranes for experimental purposes.✔ Carry out tests to evaluate the performance of new materials.✔ Collect & analyze test data, write reports, and draft specifications.✔ Prepare new coating for membrane formulations.

Alpharetta, Georgia, United States

✔ Develops, implements, and manages processes to ensure that products meet required specifications for quality, function, and reliability prior to delivery.✔ Communicates quality standards and parameters to the QA team, the product development team, and other appropriate staff.✔ Coordinates product testing processes.✔ Identifies and analyzes issues, bugs, defects, and other problems, particularly when problems recur in multiple products; recommends and facilitates solutions to these issues.✔ Reviews client, customer, and user feedback.✔ Maintains compliance with federal, state, local, and organizational laws, regulations, guidelines, and policies.✔ Design, implement and improve company quality standards.✔ Analyze data in order to find areas for growth.

Georgia

✔ Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures.✔ Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods.✔ Writing technical papers and reports, and preparing standards and specifications for processes, tests, and products.✔ Maintaining laboratory instruments, troubleshooting malfunctions, and purchasing new laboratory supplies.✔ Maintain contact with clients regarding updates/change requests for testing protocol and resolve any issues reported by customers regarding results of testing completed.✔ Compile and analyze test information to determine process or equipment operating efficiency and to diagnose malfunctions.✔ Create data charts and spreadsheets in Excel that summarized final results for method transfers and validations.

Duluth, Georgia, United States

✔ Involve in training and transfer of methods to and from QC and contract manufacturers as assigned.✔ Modify and validate analytical procedures to meet QC’s needs.✔ Support design and development of experimental protocols,✔ SOP’s, etc., consistent with cGMP/GLP.✔ Participate in special projects and department meetings via input, feedback, and execution of assigned tasks.✔ Execute special projects on analytical and instrument problem-solving.✔ Perform non-radioactive and biological QC on time and record the quality of the product.✔ Involve in procedure review and propose modifications and updates.✔ Ensure the work environment is clean and safe complying with safety and pharmaceutical regulation.✔ Conduct radiation safety duties conforming to regulations.✔ Report monthly on supplies for QC orders involving devices and reagents.✔ Contribute to industrial, R&D qualification, and validation activities and support routine maintenance.

Greater Atlanta

✔ Identify procedures and scenarios for the quality control of products and services. Design and implement testing plans for products.✔ Monitor efforts to resolve product issues and track progress.✔ Ensure that the final product satisfies the product requirements and meets end-user expectations.✔ Spot areas for improvement to enhance the product's efficiency.✔ Research the current market for similar products and compare results.✔ Ensure that safety standards and cleanliness are maintained.✔ Participate in internal assessments and audits where necessary.✔ Responsible for identifying and troubleshooting equipment problems.✔ Report or conduct an investigation on questionable test results.✔ Prepared Reference standards solutions for comparison in analytical sample testing, method development, quality analysis, and/or validation.✔ Followed Company policies, procedures including cGMP, SOP, Food Safety.✔ Created OOS report for out-of-specification test results.✔ Conducted routine metal alarm tests for Critical Control Point monitoring.

Baltimore, Maryland, United States

✔ Develop new pharmaceutical products, vaccines, medicines, and compounds such as antiseptics.✔ Provide laboratory services for health departments, for community environmental health programs and for physicians needing information for diagnosis and treatment.✔ Ensure data is recorded accurately in accordance with guidelines.✔ Remain up to date with scientific and research developments.✔ Perform laboratory analysis on all materials after appropriate sterilization.✔ Perform tests on all incoming ingredients and document all records.✔ Develop and prepare research papers and documents for all protocols.✔ Perform audits on various environmental programs and perform reviews.

Baltimore, Maryland, United States

✔ Coordinate with senior management to identify an area of interest.✔ Through modeling, form hypothetical chemical compounds to attain.✔ Utilize lab equipment to synthesize compounds.✔ Keep inventory of all chemicals with zero variance.✔ Travel to different locations for testing when requested.✔ Identify improvements that can be made to existing lab processes.✔ Prepare compounds, test solutions, and reagents to conduct tests, experiments, then advise and coordinate on test procedures.✔ Develop, improve and customize equipment, products, formulas, analytical methods, and processes.✔ Worked under GMP, cGMP, and FDA regulations.✔ Created and updated SOP and testing standards.✔ Gained knowledge of Process Excellence/Six Sigma concepts/tools.✔ Gained working knowledge of HPLC instrumentation.

Bachelor Of Science (Bs), Biology, General

High School Diploma, Biotechnology