BioMarin Pharmaceutical

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's QA team in Novato, USA, as a QA Associate. Provide vital quality oversight, support deviations/CAPAs, and ensure high-quality product delivery. Promote continuous improvement within cross-functional teams. Enjoy benefits including bonus potential, stock incentives, and comprehensi...

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 our team as a Maintenance Technician in Cork, Ireland. You will maintain critical GMP equipment in a Biologics manufacturing facility, focusing on drug product fill finish and packaging. This role requires a relevant engineering qualification and 3+ years' GMP experience. Be a key player in ...

Seeking a Manufacturing Associate for a contract role in Novato, working a rotating 12-hour night shift. You will perform biopharmaceutical manufacturing processes like cell culture and purification in a cGMP environment. The role requires a science degree or relevant experience, strong teamwork,...

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 in Cork as a Process Validation Associate. You will coordinate multi-modality validation projects in a cGMP environment for drug substance and product processes. This role requires a BA/BS degree and 8+ years of relevant GMP experience. You will execute validation protocols and supp...

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 ...

Join our Supply Chain Operations team in Cork as a Warehouse Planner. This role requires a degree and 3+ years of planning experience in a regulated manufacturing warehouse. You will manage stock levels on SAP, coordinate shipments, and ensure compliance with cGMP standards. Strong ERP knowledge ...