BioMarin Pharmaceutical Inc.

BioMarin Pharmaceutical Inc. At BioMarin, we are committed to transforming lives through genetic discovery. At BioMarin, patients are at the heart of what we do.

Applying our knowledge to make a transformative impact is not just a calling, but an obligation to those who will benefit most. The end goal has always been better lives and now we can reach more. And the more people we reach, the more our impact can grow. The BioMarin page is a place to connect with and learn about our company. We will provide company news and updates, as well as share s

tories from our patients. Our goal is to engage with our community by providing useful and interesting information, and fostering open and respectful dialogues about the diseases we seek to treat. While we are committed to fostering important relevant discussions and respect the rights of everyone to voice their opinions, we ask that users/followers of our social media channels are respectful to other members and follow our Community Guidelines. See our full Community Guidelines here: https://www.facebook.com/BioMarinOfficial/app/145740286161845

Our PRIDE Employee Resource Group (ERG) is honoring both the history of the LGBTQ+ movement and the work still ahead thr...
06/03/2026

Our PRIDE Employee Resource Group (ERG) is honoring both the history of the LGBTQ+ movement and the work still ahead through a series of events during Pride Month, including volunteer opportunities, flag raisings and participation in the Sonoma County Pride Parade. We’re looking forward to this year’s programming, which reflects the power of visibility, education, allyship and connection in building a culture of belonging. Hear from PRIDE chairs Morgan McDaniel, Carlos Calderon and Daniel Turley on what this month means to them and how authentic leadership helps turn inclusion into action.

Several of our colleagues had the opportunity to connect with members of the achondroplasia community at the annual Asso...
06/02/2026

Several of our colleagues had the opportunity to connect with members of the achondroplasia community at the annual Association for Information and Study of Achondroplasia Conference (AISAC) in Rimini, Italy. Members of the BioMarin Advocacy team met with people living with achondroplasia, their families, physicians and patient association leaders for two days of learning and connection.

Expert-led sessions explored multidisciplinary care, research updates and treatment approaches, with audience participation reflecting the community’s strong engagement and commitment to helping people around the world living with skeletal dysplasias.

It was especially meaningful to see skeletal dysplasia patient association leaders from Poland, Spain, the United Kingdom and the United States come together to strengthen international collaboration in support of the achondroplasia community.

Thank you to Marco Sessa, President of AISAC, the AISAC team and all the attendees who helped make the event so impactful.

06/01/2026

Dr. Mina Nguyen-Driver is a clinical psychologist who for years has helped young people living with rare conditions figure out how to optimize their mental health and well-being. In the first episode of our video podcast series, “Why Do I Pheel This Way,” she joins co-hosts Londyn and Connor to discuss the importance of consistency and why managing the potential cognitive effects of phenylketonuria (PKU) and high phenylalanine (Phe) levels is particularly important during adolescence.

“You want to do whatever you can do so that the brain development you’re doing right now is the building blocks for today, tomorrow, when you’re in your 30s, 40s, 50s and so on,” says Dr. Nguyen-Driver, who will join each episode in the series for a segment called 3 Phe Questions.

Watch the full first episode here: http://ms.spr.ly/6189vbrBJ

Kim Warner made a long-distance move to the San Francisco Bay Area 12 years ago and took what was, at the time, a tempor...
05/29/2026

Kim Warner made a long-distance move to the San Francisco Bay Area 12 years ago and took what was, at the time, a temporary opportunity in Talent Acquisition at BioMarin. Today, she leads our Early Talent Program, which is preparing to welcome more than 130 interns globally this summer, including approximately 50 in the United States.

In our DNA of BioMarin employee profile series, Kim reflects on her own career journey, her passion for expanding access for early-career talent, and the role connection and belonging play in building stronger pathways for the future.

Read more: http://ms.spr.ly/6187vZx3t

05/28/2026

What is a typical day like for teens living with phenylketonuria (PKU)? In the first episode of our new video podcast series, “Why Do I Pheel This Way,” hosts Londyn and Connor get real about their daily routines, how they know when their phenylalanine (Phe) levels are high and the importance of maintaining consistency while navigating the life changes that come with adolescence.

Joining the co-hosts for special segments in this episode are Londyn’s mom, Kylie, and Dr. Mina Nguyen-Driver, a clinical psychologist who specializes in working with young people with rare conditions such as PKU.

Watch the full episode here: http://ms.spr.ly/6182vZrVy

05/28/2026

What is a typical day like for teens living with phenylketonuria (PKU)? In the first episode of our new video podcast series, “Why Do I Pheel This Way,” hosts Londyn and Connor get real about their daily routines, how they know when their phenylalanine (Phe) levels are high and the importance of maintaining consistency while navigating the life changes that come with adolescence.

Joining the co-hosts for special segments in this episode are Londyn’s mom, Kylie, and Dr. Mina Nguyen-Driver, a clinical psychologist who specializes in working with young people with rare conditions such as PKU.

Watch the full first episode here: http://ms.spr.ly/6185vZrsZ

We asked members of our Asian and Pacific Islander (APIC) Employee Resource Group (ERG) to reflect on the importance of ...
05/26/2026

We asked members of our Asian and Pacific Islander (APIC) Employee Resource Group (ERG) to reflect on the importance of this community as we celebrate Asian American, Native Hawaiian and Pacific Islander (AANHPI) Heritage Month. Members expressed a deep appreciation for the ERG, noting that it provides opportunities to network, share their traditions and identities with colleagues of all backgrounds, and feel a sense of belonging.

Read what else Amy Phan and Sang Kim have to say about the role APIC plays in fostering an inclusive culture and sense of community.

We asked members of our Asian and Pacific Islander Coalition (APIC) Employee Resource Group (ERG) to reflect on the impo...
05/26/2026

We asked members of our Asian and Pacific Islander Coalition (APIC) Employee Resource Group (ERG) to reflect on the importance of this community as we celebrate Asian American, Native Hawaiian and Pacific Islander (AANHPI) Heritage Month. Members expressed a deep appreciation for the ERG, noting that it provides opportunities to network, share their traditions and identities with colleagues of all backgrounds, and feel a sense of belonging.

Read what else Amy Phan and Sang Kim have to say about the role APIC plays in fostering an inclusive culture and sense of community.

Congratulations to Kendra Gottsleben and her nonprofit Rare by Design on marking a successful fifth year of The Style Sh...
05/22/2026

Congratulations to Kendra Gottsleben and her nonprofit Rare by Design on marking a successful fifth year of The Style Show, an annual fashion event for individuals living with rare conditions and disabilities.

With more than 300 attendees, this year’s event delivered an elevated and accessible experience designed to welcome everyone. From the redesigned runway to thoughtful accessibility features throughout the space, every detail reflected the heart behind the show and its continued growth.

“We wanted to make sure accessibility was part of it,” says Kendra, who is living with mucopolysaccharidosis type VI, also known as Maroteaux-Lamy syndrome. “Seeing people from different backgrounds and abilities all together in one space is what community is all about.”

We were proud to again sponsor The Style Show and celebrate this milestone moment alongside such a remarkable community.

Learn more about Kendra and Rare by Design: http://ms.spr.ly/6182vnDSy

Employees from our Northern California sites laced up their walking shoes and came together for a company hike in suppor...
05/21/2026

Employees from our Northern California sites laced up their walking shoes and came together for a company hike in support of the National PKU Alliance Alliance initiative.

Held each May by the National PKU Alliance during PKU Awareness Month, Move Your Pheet helps raise awareness through fundraising and community engagement.

NPKUA Executive Director Catherine Warren joined approximately 100 of our colleagues for a meaningful day outdoors near our Northern California sites at China Camp State Park, where participants enjoyed beautiful weather and shared in a common purpose.

Thank you to the NPKUA and to all of our employees who participated for helping continue our longstanding support of the community. And congratulations to our NPKUA partners on another successful year of Move Your Pheet!

Learn more about Move Your Pheet: http://ms.spr.ly/6188vVXUw

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