Cameron Shore Email & Phone Number

Bellevue, Washington, United States

Kent, Washington

Sample and test shop solutions to ensure proper chemical concentration of tanks according to FAA and client specification. Testing solutions following cGLP guidelines, as well as client and FAA specifications. Accurate and timely entry of data into LIMS software following cGLP, and FAA compliant processes. Standard and solution preparation for lab use following appropriate lab methods and SOP. Peer review of laboratory testing and shop processes. Managing data, physically and virtually as to be readily available upon request. Timely communication of data, issues, solutions to problems across the shop and inside the lab. Troubleshooting and problem-solving a wide range of issues from lab instrumentation to shop solutions.

Columbia, Missouri

Performed routine experiments and procedures following applicable regulatory (DEA, EPA, FDA) guidelines in a cGMP environment for study documentation requirements as defined by protocol, method, and SOP. Carried out first level data analysis; prepared data and reports of completed projects ensuring quality for publication for clientele. Utilized various laboratory equipment, and software for product analysis as well as to develop processes and methods. Performed advanced mathematical/statistical calculations on data for clients then present said data in an easy to read report. Managed data review to ensure the quality/integrity of reports, raw data, and electronic data is up to standard with cGMP requirements as well as appropriate methods, protocols, SOP’s were followed for completeness, traceability, and accuracy. Trained staff on techniques, software, and equipment necessary to perform laboratory assignments. Worked effectively as a team and individually to meet deadlines to ensure client satisfaction and earn more loyal customers.

Columbia, Missouri

Performed routine experiments and procedures following applicable regulatory (DEA, EPA, FDA) guidelines in a cGMP environment for study documentation requirements as defined by protocol, method, and SOP. Carried out first level data analysis; prepared data and reports of completed projects ensuring quality for publication for clientele. Utilized various laboratory equipment, and software for product analysis as well as to develop processes and methods. Performed advanced mathematical/statistical calculations on data for clients then present said data in an easy to read report. Managed data review to ensure the quality/integrity of reports, raw data, and electronic data is up to standard with cGMP requirements as well as appropriate methods, protocols, SOP’s were followed for completeness, traceability, and accuracy. Trained staff on techniques, software, and equipment necessary to perform laboratory assignments. Worked effectively as a team and individually to meet deadlines to ensure client satisfaction and earn more loyal customers.

Columbia, Missouri

Performed routine experiments and procedures following applicable regulatory (DEA, EPA, FDA) guidelines in a cGMP environment for study documentation requirements as defined by protocol, method, and SOP. Carried out first level data analysis; prepared data and reports of completed projects ensuring quality for publication for clientele. Utilized various laboratory equipment, and software for product analysis as well as to develop processes and methods. Performed advanced mathematical/statistical calculations on data for clients then present said data in an easy to read report. Managed data review to ensure the quality/integrity of reports, raw data, and electronic data is up to standard with cGMP requirements as well as appropriate methods, protocols, SOP’s were followed for completeness, traceability, and accuracy. Trained staff on techniques, software, and equipment necessary to perform laboratory assignments. Worked effectively as a team and individually to meet deadlines to ensure client satisfaction and earn more loyal customers.

Kansas City, Missouri Area

Executed sample retrieval and preparation of raw materials used in intermediate and final products. Testing of raw materials, intermediates and finished products following methods and SOPs for each product to ensure quality of the product against a set specification. Accurate recording of data and observations following correct SOP’s and cGMP guidelines. Maintained awareness of and complies with regulatory and cGMP, ICH requirements for data recording and experimentation. Trained personnel on laboratory methods, equipment, and procedures. Timely communication of data to other departments and across shifts to promote teamwork and efficiency. Formation and critique of methods and SOP’s.

Graduate Certificate In Software Design And Development, Computer Software Engineering, 3.4

Object-oriented programming, data structures and algorithms in C++. Design and testing of software systems. Systems programming. Core.

Bachelor Of Science (B.S.), Biochemistry And Molecular Biology, 3.55

Activities and Societies: Central Cheer SquadBiomedical/Cellular and Molecular Biology