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.
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.