Kathleen Taggart - Project Manager Resume Simple
SUMMARY
A highly motivated, detail-oriented, and results-driven professional with over 15 years of experience in the pharmaceutical industry. Proven ability to manage multiple projects and meet deadlines.
SKILLS
  • cgmp, compliance, validation, design, sops, technical writing, usp, training, writing, glp, documentation, analytical
  • technical writing, cgmp, investigations, lc ms, safety, compliance, quality, training, validation, testing, computer, writing, hplc, troubleshooting, dissolution, fda, glp, formulation, analytical
WORK EXPERIENCES
  • 2017-12-252017-12-25

    Project Manager

    Sikorsky Aerospace Maintenance

    • Wrote training manuals, validation protocols, and SOPs for new and existing projects. Developed and implemented processes for the design and execution of the validation process.
    • Coordinated with project teams to develop and implement new and existing protocols. Developed and implemented training programs for data management.
    • Development of analytical methods, validation protocols, SOPs, and cGMP documents for compliance with USP, EP, and JP.
    • Assisted in writing and editing of the validation documents, including the development of the protocols, and the documentation of the analytical test methods.
    • Trained and mentored junior analysts on GLP and data validation projects. Provided support for troubleshooting and resolving issues. Performed data entry and statistical analysis.
    • Created and maintained project specific reports, including troubleshooting and data management. Developed and implemented a comprehensive and detailed report for the use of the analytical test.
  • 2017-12-252017-12-25

    Scientist I

    Udemy

    • Provided training and supervision to chemists, interns, and technicians in the Microbiology department. Prepared and analyzed samples, validation and data verification for compliance with GLP and cGMP requirements.
    • Performed analytical testing on raw materials, in-process, finished products, stability, and stability samples using HPLC, GC, and wet chemistry.
    • Extensive experience in writing and revising SOP's, validation protocols, and reports for the formulation of manufacturing processes. This includes troubleshooting of the instrument, and the maintenance of the HPLC.
    • Provided analytical support and troubleshooting for HPLC, GC, FTIR, and dissolution. Conducted method validation and quality assurance.
    • Performed investigations of OOS results in a timely manner and documented all corrective actions taken as necessary. Reviewed and evaluated safety reports for the department.
    • Trained in the use of HPLC, GC, and other instruments. Trained in the use of various computer programs.

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