Danielle Posey Email & Phone Number

Los Angeles, CA, US

United States

Technical writer in the regulatory affairs department.

United States

Created and edited technical documentation to support the understanding and use of products, software, and machinery in the medical device industry. Collaborated with SMEs and stakeholders to determine pertinent information. Wrote SOPs, validation protocols and reports, user manuals, IFUs, software requirement specifications, and material specifications.

Irvine, California

QA Chemistry and Microbiology. Gained skills in aseptic technique and cell culture. Improved skills in technical documentation in a FDA regulated environment. Acquired leadership skills by training peers and new hires to product testing procedures.

Irvine, California

Performed routine testing on products in the QA Chemistry laboratory. Gained skills in wet chemistry, data analysis, and technical documentation. Followed FDA requirements for medical devices and ISO 13485.

Fullerton, CA

Undergraduate student researcher in a biophysics laboratory. Utilized Matlab to analyze experimental data which was used to write a scientific paper. Fabricated microfluidics devices to be used for future experiments.