Dawn Marshall
Sanofi
Senior Director Global Sterility Assurance
- Bachelor’s degree in Chemistry and Biology. Master’s degree in Business Administration.
- Certification in Nuclear Engineering
- 24 years combined experience in FDA regulated industries. 10 years in biopharmaceuticals.
- 22 years of combined management/supervisory experience.
- 9 ½ years as Senior Director, Director or Acting Director level.
- 7 years experience teaching at the college level.
- 6 years experience in the US Navy working directly with the nuclear propulsion systems on the submarines and carriers.
- 7 years as a speaker in the pharmaceutical industry on validation concepts
- QA/QC experience in pharmaceutical, food, and environmental laboratories.
- Experience in the qualification and validation of equipment, facilities, processes, and utilities in the pharmaceutical industry including master validation planning, commissioning, IQ, OQ, and PQ authoring, reviewing, execution, and exception closure as an executor, reviewer, and manager.
- Manufacturing and technical engineering and scientific support experience in the pharmaceutical, chemical, bio-pharmaceutical, and food industries.
- Environmental and safety experience in the regulated pharmaceutical and food industries.
- Experienced in both sterile and non-sterile pharmaceutical manufacturing
- Certification in Nuclear Engineering
- 24 years combined experience in FDA regulated industries. 10 years in biopharmaceuticals.
- 22 years of combined management/supervisory experience.
- 9 ½ years as Senior Director, Director or Acting Director level.
- 7 years experience teaching at the college level.
- 6 years experience in the US Navy working directly with the nuclear propulsion systems on the submarines and carriers.
- 7 years as a speaker in the pharmaceutical industry on validation concepts
- QA/QC experience in pharmaceutical, food, and environmental laboratories.
- Experience in the qualification and validation of equipment, facilities, processes, and utilities in the pharmaceutical industry including master validation planning, commissioning, IQ, OQ, and PQ authoring, reviewing, execution, and exception closure as an executor, reviewer, and manager.
- Manufacturing and technical engineering and scientific support experience in the pharmaceutical, chemical, bio-pharmaceutical, and food industries.
- Environmental and safety experience in the regulated pharmaceutical and food industries.
- Experienced in both sterile and non-sterile pharmaceutical manufacturing