Project Manager in Life Sciences, Magle Group. I’m a dedicated and quality-focused Project Manager with a strong foundation in life sciences and a proven track record across pharma, biotech, and medical device development. My experience spans the full project lifecycle—from early-stage drug development and GMP manufacturing to regulatory submissions, stakeholder engagement, and cross-functional coordination. I’ve led CMC projects for clinical trial applications, managed DS/DP development and manufacturing, and served as the primary contact for CMOs and CROs. I oversee budgets, risk planning, and supply agreements, ensuring compliance with ISO 13485, GMP, and Class II/III medical device standards. Earlier in my career, I also served as QC Lead in GMP stem cell manufacturing, contributing to audits, sample coordination, and process improvements. I’m passionate about combining science, quality, and teamwork to deliver meaningful results. I believe people make the workplace, and I bring a positive, empathetic, and solution-oriented mindset to every project and team I lead.