Jill Green

Assistant Regulatory Operations Manager @ KalVista Pharmaceuticals

About Jill Green

Jill Green is an Assistant Regulatory Operations Manager at KalVista Pharmaceuticals, Inc., with a strong background in quality assurance and regulatory operations. She has over 13 years of experience in the pharmaceutical industry and has held various roles that demonstrate her expertise in managing regulatory submissions and enhancing administrative efficiency.

Work at KalVista Pharmaceuticals

Jill Green currently serves as the Assistant Regulatory Operations Manager at KalVista Pharmaceuticals, Inc., a position she has held since 2021. In this role, she leverages her extensive experience in regulatory operations to manage compliance and documentation processes. Her responsibilities include ensuring that regulatory submissions meet industry standards and facilitating communication between internal teams and external regulatory bodies.

Previous Experience in Regulatory Operations

Before joining KalVista Pharmaceuticals, Jill Green worked for a decade at Porton Biopharma Ltd as a Validation Document Controller. In this capacity, she developed a strong foundation in quality assurance and validation processes. Additionally, she held various roles in regulatory operations, including a position as a QA Documentation Officer at Public Health England, where she managed quality assurance documentation for two years.

Education and Expertise

Jill Green has a robust educational background in business and administration. She studied at Severn Business School, earning an EBMA Advanced Level 5 Diploma in Business Administration. Her qualifications also include a Level 3 Legal Secretary Diploma from New Skills Academy and an EBMA Level 4 Diploma in Administrative Management. She has further enhanced her skills with courses in operations management and Microsoft Office.

Achievements in Regulatory Compliance

Jill Green has played a critical role in managing audits, acting as the interface for both internal and external audits, including those by the FDA and MHRA. Her expertise in GxP guidelines has been instrumental in enhancing customer-focused environments. She is recognized for developing innovative solutions and implementing process improvements that have increased administrative efficiency and customer satisfaction.

Career Progression and Skills

Jill Green's career spans over 20 years, during which she has transitioned through various roles in regulatory operations and quality assurance. Her experience managing SEND datasets is crucial for regulatory submissions in the pharmaceutical industry. She excels in leadership roles, inspiring team improvements while maintaining positive dynamics, and has contributed to several high-profile projects by ensuring effective documentation flow.

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