Hi, I'm Lizzandra and I'm a professional with over 10 years of experience in validation testing/strategy/protocol development and quality compliance. Some of my accomplishments include:

• Leading multiple teams to develop and implement project execution plans without operational impact, on-time, and within budgets.

• I am also adept in system and process assessments, regulatory compliance, and preparing documents for equipment, utilities, and computer systems.

I work closely with teams of engineers and contractors to streamline and improve software processes.

Georgia is the Director & Head of Promotional Review and Operations (PRO) at Alexion AstraZeneca Rare Disease, leading MLR transformation across multiple brands and indications. She specializes in modernizing review processes, embedding AI-driven insights, and fostering a culture of accountability to accelerate launch readiness while ensuring compliance. A people-centered leader, Georgia prioritizes team development, clear communication, and trust-based influence, and also leads philanthropic initiatives through the Edna May Morris Foundation.

Highly effective and accomplished Information Technology Leader and Technical Project Manager with extensive multi-industry experience in Pharmaceuticals and Biotechnology. Recognized for exceptional expertise in business analysis for Life Science in both GxP and non-GxP environments. Known as a collaborative leader, team builder and mentor skilled at leveraging technology to drive business solutions from planning through execution.

With over 18 years of experience in pharmaceutical manufacturing and quality assurance, Hugo currently serves as General Manager at Alcon, overseeing operations in Fort Worth, Texas. He has held leadership roles in manufacturing, quality assurance, and compliance at Alcon and Novartis across the US, UK, and Brazil. His expertise spans quality management systems, regulatory compliance, process validation, and continuous improvement, driving operational excellence while ensuring adherence to cGMP and global regulatory standards.

Technical writer and quality professional focused on clear, consistent communication in regulated environments. I specialize in deviation investigations, CAPA reporting, and continuous improvement documentation—translating technical findings into actionable insights.

I believe that quality work starts with quality writing. My goal is to make every report, guide, and process document not only compliant but understandable. I work with Excel, Teams, Word, PowerPoint, Dynamic, Veeva, and Veeva Vault in my daily line of work.

I also have a background in Lean Manufacturing, Six Sigma, TRS, SAP, and MES. Feel free to contact me at my email as I check it everyday.

The Pop in Your Job: What drives me in my work is knowing I am making a difference in patient care. I strive to ensure quality is upheld and to ensure proper and timely manufacturing so that all patients can receive the care they need. The medicine we create improves quality of life and even saves some as well.

Alexion, AstraZeneca Rare Disease is focused on pioneering new possibilities for the rare disease community. We are driven by a mission to change what it means to live with a rare disease. A leader in rare disease for more than three decades and today continues to build a diversified pipeline across disease areas with significant unmet need, using an array of innovative modalities. As part of AstraZeneca, Alexion is continually expanding its global geographic footprint to serve more rare disease patients around the world. It is headquartered in Boston, US. Alexion’s pioneering legacy in rare disease is rooted in being the first to translate the complex biology of the complement system into novel medicines. Alexion pushes boundaries to accelerate the discovery of life-changing medicines. Headquartered in Boston, Massachusetts, Alexion has offices around the world and continues to expand its reach to benefit more people globally.

We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet. For more information, visit www.astrazeneca.com.

We are a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We prioritise innovation in specialty medicines and vaccines to prevent and treat disease.

Alcon helps people see brilliantly. As the global leader in eye care with a heritage spanning over 75 years, we offer the broadest portfolio of products to enhance sight and improve people’s lives. Our Surgical and Vision Care products touch the lives of more than 260 million people in over 140 countries each year living with conditions like cataracts, glaucoma, retinal diseases and refractive errors. Our more than 25,000 associates are enhancing the quality of life through innovative products, partnerships with Eye Care Professionals and programs that advance access to quality eye care. Learn more at www.alcon.com.

As a premier, independently owned CDMO with over 65 years of sterile injectable manufacturing experience, Simtra BioPharma Solutions offers world-class cGMP sterile fill/finish, technical expertise, quality service, and a uniquely collaborative approach. Pharmaceutical and biotech companies partner with us when they face formulation challenges, clinical supply hurdles, surges in demand due to market fluctuations, or risk mitigation concerns. Our teams are driven to offer our clients tailored and versatile solutions to help them bring their products to market so they can get to the patients who need them. (Simtra is a tradename of Baxter Oncology GmbH and Simtra US LLC).