Pete Piliero, M.D.

Pete Piliero, M.D.

Pete Piliero, M.D.

Pete Piliero, M.D.

Vice President of Medical Affairs

Peter J. Piliero, M.D., is an Infectious Disease specialist and global Medical Affairs leader, having held significant clinical and leadership positions over the last 28 years at GSK Consumer Healthcare, Boehringer Ingelheim, Merck, Mallinckrodt and Albany Medical College.

Pete joined Melinta from GSK Consumer Healthcare, where he led Medical Affairs Americas. Prior to that role, he spent 12 years at Boehringer Ingelheim in Clinical Development and Medical Affairs. There, he led high-performing teams in various therapeutic areas including Virology, Immunology, CNS, Metabolism and Women’s Health. At Merck, Pete led Global Medical Information followed by U.S. Medical Affairs. At Mallinckrodt, Pete was responsible for global Scientific Affairs as well as the overall strategic planning, governance and management of the global Field Medical organization.

Prior to joining the pharmaceutical industry, Dr. Piliero was Associate Professor of Medicine at Albany Medical College. He practiced there for 11 years as an Infectious Disease and HIV specialist, providing patient care and directing the Clinical Pharmacology Studies Unit.

Since 2017, Pete has been an active member of the Medical Affairs Professional Society. He is currently a member of the Board of Directors and the Vice Chair of the Executive Committee.

 

I am honored to work alongside this truly committed team to achieve our vision – ensuring that all patients with life-threatening illnesses who need our innovative therapies will receive them

Jisoo Park

Jisoo Park

Jisoo Park

Chief Business Officer

Jisoo is a global pharmaceutical business development leader with a proven track record. Previously, Jisoo served as Vice President of Business Development and M&A at Covis Pharma. At Covis, Jisoo led global business development and M&A, including transformational buy-side and sell-side M&A, licensing and financings. In less than five years, Jisoo led seven deals worth roughly $2 billion in transaction value, helping expand the organization beyond the U.S. and into more than 50 markets.

Prior to Covis, he was an investment banker in J.P. Morgan’s Global Healthcare team in New York and San Francisco, where he advised companies in the pharmaceuticals, biotech and life sciences industries on M&A, equity and debt financings.

He holds a B.S. in Economics and Statistics from Carnegie Mellon University.

“Melinta is on a mission to make the most meaningful impact for patients with life-threatening illnesses and I’m excited to join the team in the middle of such great momentum. I look forward to working with this truly committed team toward continued growth and expansion to serve patients in need in the U.S. and beyond.”

Melinta is on a mission to make the most meaningful impact for patients with life-threatening illnesses and I’m excited to join the team in the middle of such great momentum. I look forward to working with this truly committed team toward continued growth and expansion to serve patients in need in the U.S. and beyond.

Doug Girgenti, M.D

Doug Girgenti, M.D

Doug Girgenti, M.D

Vice President of Drug Development

Doug is a seasoned physician with more than twenty-five years of clinical and industry experience. After studying genetics and microbiology at Cornell University and Cold Spring Harbor Laboratory, and medicine at SUNY at Stonybrook School of Medicine, Doug completed residency training in Internal Medicine and Pediatrics through the Yale University School of Medicine. He served as a practicing Internist and Pediatrician in New York for about ten years, last serving as Medical Director of ARC of Rockland, NY, caring for adults and children with cognitive and other developmental disabilities. Since transitioning to clinical research and development, he has led global clinical programs for Wyeth, Pfizer, Boehringer-Ingelheim, and Magenta Therapeutics, developing investigational vaccines targeting Staphylococcus aureus and invasive pneumococcal disease, and numerous small and large molecules in the fields of immunology, stem-cell transplantation, nephrology, ophthalmology, cardiology, and rare diseases.

 

I look forward to helping lead the way for more sustainable growth through clinical and developmental success while keeping patients at the center of our legendary future.

Kelley Ford

Kelley Ford

Kelley Ford

Vice President, Manufacturing and Supply
Technical Operations, Supply Chain, Quality

Kelley Ford is a forward-thinking technical leader in the pharmaceutical industry with a depth of experience across the product lifecycle for analytical, drug substance, and drug product. She’s been an integral part of Melinta’s success since 2016.

Before joining our team, Kelley served as Director of Manufacturing Science & Technology at AbbVie, where she managed the technical operations and third-party manufacturing process for specific product lines.

Previous to that, she held several technical operations positions at AbbVie/Abbott. For nearly 20 years, she was intricately involved in the development, manufacturing, and lifecycle support for several globally marketed pharmaceutical products.

She began her career at Sandoz as a process development chemist.

Kelley holds a B.A. in General Science from the University of Iowa, a B.S. in Chemistry from Elmhurst College, and a Ph.D. in Organic Chemistry from Northwestern University.

We don’t just create life-changing pharmaceuticals. We create value, innovations, a focus on under-served patients and disruptive shifts in markets where we know there’s a better way forward.

Susan Blum

Susan Blum

Susan Blum

Interim Chief Financial Officer, Vice President of Finance & Chief Accounting Officer

Susan is a financial and accounting leader with more than 20 years of diverse experience strengthening corporate financial strategy, efficiencies, and controls. She’s been an integral part of Melinta’s financial and accounting team since 2016.

Before joining Melinta, Susan served as Corporate Controller at Textura, where she oversaw the accounting function and played a lead IPO role with responsibility for centralizing accounting functions post-acquisition.

Before Textura, she held leadership roles at Orbitz Worldwide, Inc., where she directed global technical accounting processes. And before that, Susan managed the SEC reporting and revenue functions at Facet Biotech and PDL BioPharma.

Susan began her career in public accounting at Ernst & Young, where she worked with a diverse client base ranging from large, public international SEC engagements to development-stage enterprises.

She holds a B.S. in Business Commerce from Santa Clara University and is a certified public accountant.

Melinta is well-positioned for growth and financial sustainability, the two things that will help us maintain our momentum and take big steps forward. It’s exciting to think about what our future holds and the success we’ll achieve.

Jennifer Sanfilippo

Jennifer Sanfilippo

Jennifer Sanfilippo

General Counsel

Jennifer is a seasoned life sciences industry executive with demonstrated success in general management, legal, and compliance.

Before Melinta, Jennifer held several leadership roles at The Medicines Company. She led legal and compliance counsel for multiple business units guiding commercial, medical, market access, and regulatory activities in those roles

Before The Medicines Company, Jennifer was an attorney at Porzio, Bromberg & Newman, P.C., a law firm specializing in the life sciences industry. She advised pharmaceutical, medical device, and biotech companies on a variety of legal, regulatory, and compliance issues.

Jennifer holds a B.A. in History, magna cum laude, from New York University and a J.D. from the Rutgers School of Law, where she was managing editor of the Rutgers Law Review.

 

I’m proud of our commitment to each other and our patients, and how we operate with quality and integrity always in mind. We’re small but nimble, and our culture of collaboration means that we can make a big impact for our patients.