Marilyn Panahi
About Marilyn Panahi
Marilyn Panahi is the Vice President of Quality with over 35 years of experience in the life science industry, specializing in regulatory and manufacturing quality assurance.
Marilyn Panahi Vice President of Quality
Marilyn Panahi serves as the Vice President of Quality in the life science industry. With over 35 years of experience, she has been instrumental in guiding quality assurance processes across various companies. Her roles have spanned both public and private life science companies located primarily in the San Diego area. Her career is marked by her extensive expertise in regulatory and manufacturing quality assurance, focusing on ensuring compliance and maintaining high standards of quality.
Marilyn Panahi Education and Specialized Training
Marilyn Panahi received her Bachelor of Science degree in Microbiology from San Diego State University. She furthered her education with specialized certificates from the University of California San Diego in Science of Regulatory Affairs for the Drug and Biologic Industry and in Quality Assurance/Control for the Drug and Biologic Industry. Additionally, she completed the Oriel Stat A Matrix Class for Quality Systems for Medical Devices, focusing on FDA’s QSR and ISO 13485 compliance.
Marilyn Panahi Experience in Life Science Industry
With a career spanning more than three decades, Marilyn Panahi has accumulated extensive experience in the life sciences sector. She has held various quality assurance leadership roles, managing and implementing GLP and GMP quality systems. Her work has been critical in developing robust regulatory and quality frameworks within the organizations she has served. Her expertise ensures that companies meet stringent industry standards, thereby maintaining product safety and efficacy.
Marilyn Panahi Quality Systems Implementation
Marilyn Panahi has a deep background in the implementation and management of GLP and GMP quality systems. Her knowledge includes establishing processes that comply with regulatory requirements and maintaining high standards of practice. Her role often involves identifying areas for improvement and introducing best practices that ensure ongoing compliance and enhance the overall quality of manufacturing processes in the life science field.