Jill Green Email & Phone Number

I am a dedicated, reliable and organised business professional with a versatile administrative support skill set developed from many years’ experience organising and supporting departments within the customer service, financial and pharmaceutical industries. I currently support regulatory document management functions, investing my time in understanding the requirements and regulations for global submissions to regulatory authorities. Every day is different from quality control checking, formatting and publishing of pharmaceutical documentation, to managing SEND datasets, to discussing clinical stage progressions. I can decipher priorities and have the maturity to deal with sensitive and confidential information, whilst ensuring attention to detail throughout. I am challenged by situations that necessitate diligence and precision in demanding and stimulating environments to meet accuracy, quality and agreed service levels.Prior to career advancement into the regulatory field, I spent 13 years at a Final Drug Product company supporting key quality and engineering aspects such as document management, change control and quality administrations, transitioning within roles in Quality Assurance and Validation.With an understanding of GxP guidelines, I apply this knowledge to all aspects of my work and actively transfer this application within the customer focused environments, communicating and negotiating at all levels, building strong and respectful working relationships. I excel in resolving employer challenges by developing innovative solutions, systems and implementing process improvements proven to increase administrative efficiency and customer satisfaction. I have successfully contributed and supported several high profile projects by using my organisational skills and applying a detailed-orientated approach to ensure there is effective information flow and adequate trace-ability of documentation as changes and upgrades commence.I have been the critical interface for both internal and external audits, independently and promptly delivering requested information during audits and inspections (FDA, MHRA, Independent). I am challenged in positions where I can utilise my existing skillset but also transfer my knowledge and experience by leading others, inspiring improvements whilst retaining positive team dynamics.

Listed skills include Pharmaceutical Industry, Quality Assurance, Gmp, Change Control, and 45 others.