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Cindy Rogers
Cindy Rogers
research associate | Sana Biotechnology, Inc.
Massachusetts, Webster, United States
Cindy Rogers
Summary
Cindy Rogers is an accomplished Executive Director specializing in GCP/GLP Quality Assurance, with over 20 years of experience in bioanalytical assay development. She has a robust background in evaluating and quantifying biologics and small molecules across pre-clinical and clinical settings. Her extensive knowledge of GLP and GCP regulations is complemented by her experience in QA auditing across various organizations including CTOs and CROs. Cindy has held significant roles at reputable companies such as Sana Biotechnology and bluebird bio, demonstrating her leadership in the field. She holds a BS in Biomedical Science from Framingham State University. Her career reflects a commitment to excellence in quality assurance and regulatory compliance in the biopharmaceutical industry. Cindy is known for her strategic thinking and ability to navigate complex regulatory environments, making her a valuable asset in any organization.
Cindy Rogers
Work Experience
Executive Director GCP/GLP QA at
Sana Biotechnology, Inc.
August 2022 - Present
Cindy Rogers
Education
Framingham State University, BS, biomedical science
January 1984 - January 1988
Frequently Asked Questions about Cindy Rogers
What is Cindy Rogers email address?
Cindy Rogers's primary email address is ************@sana.com. To view the full verified email and additional contact details, sign up for free with Muraena.
What company does Cindy Rogers work for?
Cindy Rogers is a research associate at Sana Biotechnology, Inc..
Where Cindy Rogers graduated from?
Cindy Rogers holds a degree in null from Framingham State University.
How can I directly contact Cindy Rogers?
To contact Cindy Rogers directly, you can use the email address ************@sana.com. Complete contact information is available upon registration with Muraena.
Who is Cindy Rogers?
Cindy Rogers is an accomplished Executive Director specializing in GCP/GLP Quality Assurance, with over 20 years of experience in bioanalytical assay development. She has a robust background in evaluating and quantifying biologics and small molecules across pre-clinical and clinical settings. Her extensive knowledge of GLP and GCP regulations is complemented by her experience in QA auditing across various organizations including CTOs and CROs. Cindy has held significant roles at reputable companies such as Sana Biotechnology and bluebird bio, demonstrating her leadership in the field. She holds a BS in Biomedical Science from Framingham State University. Her career reflects a commitment to excellence in quality assurance and regulatory compliance in the biopharmaceutical industry. Cindy is known for her strategic thinking and ability to navigate complex regulatory environments, making her a valuable asset in any organization.
Cindy`s contact details
************@sana.com
************@genzyme.com
*******@bluebirdbio.com
Colleagues
Operations Roles of Increasing Responsibility [Technician to Supervisor]
Senior Director
Research Fellow
Columnist
Intern, Biochemical and Cellular Pharmacology
Assistant Professor of Molecular Biology
Postdoctoral Fellow
Formulations scientist
Finance Specialist / Research Operations Specialist
Sr Scientist & Sr Group Leader