Rebecca Perrine (Atkins)

Rebecca Perrine (Atkins)

Senior Regulatory Affairs Specialist @ Boston Scientific

About Rebecca Perrine (Atkins)

Rebecca Perrine (Atkins) is a Senior Regulatory Affairs Specialist with extensive experience in regulated GMP/GLP laboratory environments, focusing on medical devices, pharmaceuticals, and biologics.

Current Role

Rebecca Perrine (Atkins) currently serves as a Senior Regulatory Affairs Specialist. She has been in this role since 2020. She focuses on ensuring compliance with regulatory standards for medical devices, pharmaceuticals, and biologics. Her extensive experience in navigating the regulatory landscape aids in streamlining product approval processes.

Previous Experience

Rebecca has held various roles in her career. Key positions include Regulatory Affairs Specialist II (2017-2020) and Biocompatibility and Safety Scientist (2017) in Marlborough, MA. She also worked as Project Development Advisor (2012-2014) and Study Coordinator (2012) in Northwood, OH. Earlier roles include Technical Support Specialist and Advanced InVitro Technologist in Toledo, OH, and Molecular Biologist at Uniformed Services University.

Educational Background

Rebecca Perrine (Atkins) studied at Wittenberg University, earning a Bachelor of Science in Biochemistry/Molecular Biology from 2006 to 2010. Her academic background laid a strong foundation for her career in regulatory affairs, focusing on biocompatibility and chemical characterization.

Expertise in Regulatory Affairs

Rebecca possesses extensive experience in regulated GMP/GLP laboratory environments. Her work spans medical devices, pharmaceuticals, and biologics, with specific expertise in viral mutagenesis, human cell culture, and mammalian cell culture. She has implemented numerous research-driven best practices to enhance regulatory compliance and effectiveness.

Focus on Biocompatibility

In the regulatory affairs domain, Rebecca has a strong focus on biocompatibility and chemical characterization. Her methodical approach aids in addressing challenges in the medical device industry, ensuring that products meet stringent regulatory standards for safety and efficacy.

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