About Phoenix

My career in the pharmaceutical space began in biopharma as a Quality Assurance Specialist. Having been groomed to view things with a quality mindset in a rigid cGMP environment, I thought it would be beneficial to jump to the operations side where I could employ the quality mindset to make impactful decisions. Following a stint as a Production Supervisor, I transitioned to the 503A/503B compounding space to learn another sect of the industry, while getting an early opportunity at a management position. As the firm's Sterile Manufacturing Manager, I helped develop a cGMP culture focused on right first-time execution. Additionally, I spearheaded the development of SOPs, Batch Records, and Work Instruction to ensure repeatability of processes while ensuring all data was documented accordingly. My goal with Phoenix is to continue down this path, keeping patient safety and quality assurance at the forefront, while partnering with firms across the country who may need some guidance. Let Phoenix assist your firm to elevate with confidence!