About Loyal Loyal is a clinical-stage veterinary medicine company developing longevity drugs for dogs. Our mission is to help dogs live longer, healthier lives. Were pioneering a new category of veterinary prescription drugs that proactively and
Position Summary The Executive Director, CMC QA will provide strategic, operational, and technical quality leadership across all Ultragenyx programs inclusive of biologics, small molecule, gene therapy, and ASO. This leader will oversee CMC QA responsibilities spanning program QA
Cardiology Administrative Coordinator The Cardiology Administrative Coordinator will be responsible for performing clerical, scheduling, and administrative functions that support the daily operations of the cardiology departments. This individual will collaborate with clinical staff to provide efficient,
Position Summary ultra-focused – Work together to fearlessly uncover new possibilities The Senior Manager, CMC QA will be responsible for the Product Complaints, Annual Product Quality Review and CMC Change Control Review Board programs and will maintain strategic
Executive Director, CMC QA Novato, CA; South San Francisco, CA Why Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of
CMC Asset Lead As the CMC Asset Lead, you will be an integral part of the PO&T Nephrology team, focusing on the development and launch of Biogens nephrology assets. Your initial focus will be on overseeing a critical
BioMarin is seeking a highly motivated candidate with drug product development experience to oversee formulation development and manufacturing activities. The role may serve as SME in formulation development or as DP Partner Team Lead, coordinating with
BreezeBio is a rapidly-growing, early-stage company that is developing a proprietary and novel delivery platform with the potential to transform genetic medicine. Our interdisciplinary team works together across chemistry, payload design, formulation, and screening and preclinical
Ultragenyx Pharmaceutical in California seeks an Executive Director, CMC QA to provide strategic, operational, and technical quality leadership across biologics, small molecules, gene therapy, and ASO. You will lead a team of 8–12 professionals and ensure phase-appropriate
BreezeBio in South San Francisco, CA is seeking a Senior Consultant to lead CMC development and manufacturing activities for late‑phase programs. You will manage in‑house and CDMO manufacturing, ensure timing aligns with development plans, and drive regulatory-ready
Hybrid Position: San Francisco (or) San Diego My client is a late-stage clinical biopharmaceutical company focused on addressing some of the most challenging mechanisms of cancer resistance through innovative, science-driven drug development. This opportunity offers the
Ultragenyx is seeking a Senior Manager, CMC QA in Novato, California. This role involves overseeing product quality reviews, managing the Change Control Review Board, and ensuring compliance with regulatory standards. The ideal candidate has over 8 years
SUMMARY/JOB PURPOSE (Basic purpose of the job): Exelixis is expanding its Antibody-Drug Conjugate (ADC) platform to advance a growing pipeline of oncology bioconjugates. We are seeking a Senior Principal Scientist with deep expertise in conjugation chemistry
Olema Oncology is a clinical-stage biopharmaceutical company committed to transforming the standard of care and improving outcomes for patients living with breast cancer and beyond. It’s an exciting time to be part of Team Olema, with
Who We Are BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis
Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle
At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented
SUMMARY/JOB PURPOSE: The Executive Director, Regulatory Affairs has oversight for all regulatory activities for new development programs, pre-IND through BLA/NDA and post-approval. Responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Additionally,