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Research Associate 1

Ireland, Cork · Job Posted March 19, 2026
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Job Description

Overall Purpose of the Role Perform and document scientific experiments in collaboration with cross‑functional stakeholders as part of the BCoE or site strategy, and/or in support of BioMarin’s commercial and clinical product portfolio.

Job Responsibility

  • Perform and document scientific experiments in collaboration with cross‑functional stakeholders as part of the BCoE or site strategy, and/or in support of BioMarin’s commercial and clinical product portfolio
  • Execute defined procedures under close supervision to support BCoE studies and investigation activities involving lab‑scale upstream processes in a multi‑product lab
  • Identify routine experimental issues and resolve them by following SOPs and BPDs
  • Produce accurate, reproducible data and maintain laboratory quality through adherence to safety and SOPs
  • Perform daily mammalian cell culture expansion and bioreactor monitoring, including sampling and in‑process analysis using standard bioprocess analytical equipment
  • Execute and complete projects with supervision
  • Generate, review, and share raw data with peers and project leads
  • Maintain up‑to‑date documentation of laboratory work, including storage and archiving in accordance with GLP
  • Support maintenance of lab instructions, BPDs, SOPs, and templates
  • Support maintenance and calibration of lab equipment with required documentation
  • Contribute to evaluation of new equipment
  • Demonstrate strong teamwork and communication skills
  • Actively contribute to maintaining and improving workplace and laboratory safety
  • Comply with applicable GxP regulations, SOPs, HSE, and other laboratory guidelines
  • May be required to work periodically outside normal business hours

Requirements

  • Bachelor’s degree or higher in Science or Engineering (or equivalent experience)
  • Minimum of 1 year of experience in the pharmaceutical industry or equivalent strong laboratory experience
  • Working knowledge of pharmaceutical regulatory requirements appropriate to the role and understanding of cGMP manufacturing processes for biologics
  • Learn core scientific techniques quickly and demonstrate understanding of key scientific principles and protocols (batch, fed‑batch, perfusion processes)
  • Understanding of microbial cell expansion and fermentation processes is desirable
  • Understanding of downstream purification processes is desirable

Nice to have

  • Understanding of microbial cell expansion and fermentation processes
  • Understanding of downstream purification processes

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