Hermine Cobb - Sales Associate Resume Simple
To obtain a position in a company that will allow me to utilize my skills and experience to benefit mutual growth and success. I am a self-motivated, dependable, and a team player.
  • auditing, testing, investigations, writing, process development, filing, responsible, fda, data entry
  • change control, testing, supervisor, compliance, training, responsible, audits, research, implementation
  • 2017-12-252017-12-25

    Sales Associate

    Global Services

    • Management of laboratory investigations, including filing, archiving, and tracking of samples. Perform data entry and review.
    • Performed method development, validation, and stability studies for the FDA and DEA audits. Developed and implemented new cleaning procedures and processes.
    • Member of the team responsible for the development and validation of new product testing and troubleshooting. Reviewed and revised the technical documents.
    • Assisted in the writing of standard operating procedures (SOPs) and protocols. Reviewed and evaluated QC documents for accuracy and completeness.
    • Performed auditing of data for accuracy and completeness. Maintained accurate and complete records of all study activities. Assisted in the development and revision of standard operating procedures.
    • Performed technical support for the development of new product line. Supported the development of a robust product line. Collaborated with the Architect and the project team to develop and implement new products.
  • 2017-12-252017-12-25

    Research Associate III

    South County Hospital

    • Responsible for the implementation and training of new SOP and procedures in compliance with cGMP and OSHA regulations. Maintained records and files for all testing.
    • Completed projects as assigned by supervisor and cGMP. Participated in the development and validation of new methods. Trained new employees.
    • Performed internal audits of the research department and developed a new method for eliminating the occurrence of repeat investigations. Also, I was trained in the process of the validation of the company.
    • Performed technical support for the development of new and existing cGMP and current standard operating procedures (SOPs) and protocols.
    • Development of a new method for the validation of a new instrument for the detection of residual solvents. The results were Used in the investigation of the problem.
    • Worked with cross functional teams to ensure timely completion of projects. Performed routine and complex assays on the development of the final product.


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