BioMarin Pharmaceutical

Seeking a Customer Engagement & Marketing Manager in Shanghai. Lead external partnership projects for Voxzogo® in China, managing timelines, budgets, and cross-functional teams. Requires 5+ years pharma industry experience, strong project management skills, and fluency in English.

Join BioMarin's Technical Operations team in Novato as a Manufacturing Associate. You will support cutting-edge biopharmaceutical manufacturing processes, including cell culture and protein purification. This role requires a science degree or relevant experience in a regulated GMP environment. We...

Join our team in Cork as a Packaging Technician. You will operate the packaging suite, ensuring safety, quality, and cGMP compliance. Ideal candidates have 2+ years of team experience and strong attention to detail. This role offers a dynamic, regulated environment in the pharmaceutical sector.

Join BioMarin in Cork as a Maintenance Planner Scheduler. You will plan and schedule all maintenance activities in our biologics manufacturing facility. The role requires expertise in CMMS and GMP experience within the bio-pharmaceutical industry. Be a key liaison, ensuring efficient operations a...

Join BioMarin's QA team in Cork as a Packaging Specialist. Provide vital Quality oversight for pharmaceutical packaging, ensuring GMP compliance and process improvement. This role requires 5+ years of QA experience in pharma/biotech and strong knowledge of FDA/EMEA regulations. Drive quality init...

Lead our Global Pharmacovigilance (GVP) Compliance team, ensuring adherence to FDA, EMA, and global regulations. You will manage the GVP audit program, support regulatory inspections, and mitigate compliance risks. This senior role offers competitive benefits and requires 10+ years of PV quality/...

Join BioMarin's high-performing team in Cork as a Biotechnician. This role requires a Bachelor's in Biotechnology or related field and proficiency in manufacturing equipment. You will perform cell culture/purification operations, troubleshoot processes, and author GMP documentation. We seek an or...

Join our team in Cork as an Operations Compliance Specialist. You will manage Manufacturing Operations documentation and ensure GMP/GDP compliance within a regulated healthcare environment. The role requires expertise in technical writing, data analytics, and Veeva QMS. This is a key position for...

Join our External Quality team in Cork as a QA Quality Specialist. You will manage key Quality Systems like Deviations, CAPAs, and Change Controls, ensuring regulatory compliance. The role involves data analysis, cross-functional collaboration, and driving continuous improvement. A Bachelor's in ...

Lead a high-performing cell biology and analytical pathology team in San Rafael. Drive preclinical research for rare genetic diseases, leveraging your PhD and 10+ years' expertise in disease models and histopathology. Enjoy competitive benefits including medical insurance, bonus potential, and st...

Join our Enzymatic and Metabolic In Vivo team in Petaluma, CA, as a Scientist II. You will design and execute key rodent studies to develop novel therapeutics for genetic metabolic disorders. This role requires a PhD with extensive in vivo metabolic disease research experience. We offer competiti...

Lead regulatory strategy and submissions for global clinical programs as a Regulatory Affairs Manager. This US-based role requires a life sciences degree and 4+ years of nonclinical/clinical RA experience. You will prepare for health authority interactions and manage IND/CTA maintenance. The posi...