Ruby Survi Email & Phone Number

Boston, Ma, Us

Boston, Ma, Us

Student MemberAs a current student member of the ISPE Boston Area Chapter, I am actively engaged in the following roles:- Networking: Building and expanding my professional network by connecting with industry leaders and fellow regulatory affairs professionals.- Educational Development: Participating in seminars, workshops, and conferences to stay abreast of the latest developments and best practices in pharmaceutical engineering and regulatory affairs.- Professional Growth: Engaging in educational and training programs to enhance my skills and knowledge in regulatory affairs, with a focus on ensuring the safety and efficacy of medical products.- Community Involvement: Collaborating with peers and experienced professionals to contribute to the advancement of regulatory practices and standards within the pharmaceutical industry.This role is an exciting opportunity for me to deepen my understanding of regulatory affairs, stay updated on industry trends, and contribute to the ISPE community. I am committed to leveraging this experience to further my career and make a positive impact in the field.

Collaborated with senior researchers and faculty members in conducting literature reviews, data collection, and analysis related to pharmaceutical research projects.Leadership role in coordinating project activities, including setting timelines, delegating tasks, and ensuring project milestones are met.Organized and maintained research data, ensuring accuracy and confidentiality. Utilized appropriate software tools for data analysis and visualization.

Assisted faculty members in preparing for lectures, workshops, and laboratory sessions. Help set up equipment, distribute materials, and ensure a conducive learning environment for students.

Hyderabad, Telangana, India

Conducted routine quality checks on raw materials, intermediates, and finished products to ensure compliance with established quality standards and regulatory requirements.Assisted in the review and updating of Standard Operating Procedures (SOPs) related to quality control and assurance processes, contributing to enhanced operational efficiency.Participated in internal audits and inspections to identify areas for improvement and ensure adherence to Good Manufacturing Practices (GMP) and company quality policies.Supported the validation of analytical methods and equipment, ensuring accuracy and reliability in product testing procedures.Collaborated with cross-functional teams to investigate and resolve quality-related issues, implementing corrective and preventive actions (CAPAs) to mitigate risks and improve product quality.Contributed to the documentation and management of deviation reports, change controls, and non-conformance events, ensuring timely resolution and compliance with regulatory requirements.Engaged in training sessions and workshops on quality assurance principles and practices, enhancing knowledge and understanding of pharmaceutical quality management systems.

Master Of Science - Ms, International Relations And Affairs, 4.0/4.0 Gpa

8.3/10.0 Gpa

Intermediate Education, 9.6/10 Gpa

Secondary Education