GMP QC Microbiology Scientist

BioSpace

Ireland (WV)

On-site

USD 42,000 - 99,000

Full time

2 days ago
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Job summary

Regeneron is seeking a QC Microbiology Associate Scientist/Scientist to join the QC Tech Resources team in Raheen, Limerick. You will validate methods and equipment for sterility, bioburden, and endotoxin testing, write technical documents, and culture organisms for investigations and development.

The role emphasizes GMP QC laboratory experience, aseptic techniques, and strong problem-solving skills, with opportunities to contribute to regulatory inspections and continuous improvement.

Qualifications

  • Experience in GMP QC laboratories and aseptic techniques.
  • Ability to validate methods and equipment for sterility, bioburden, endotoxin testing, and microbial identifications.
  • Proven ability to write technical documentation and investigations within a regulated environment.

Responsibilities

  • Validate methods and equipment for sterility, bioburden, endotoxin testing, and microbial identifications.
  • Write technical documentation including position papers, validation reports and investigations.
  • Culture organisms, conduct research, and characterize them for investigations and development.
  • Review new test procedures and assays for accuracy and compliance.
  • Evaluate new methodologies, techniques, and equipment as needed.
  • Oversee contract laboratory testing to ensure quality and compliance.

Skills

Troubleshooting
Problem solving
Attention to detail
Written and oral communication

Education

BS/BA in Microbiology or related field

Job description

Regeneron is seeking a QC Microbiology Associate Scientist/Scientist to join the QC Tech Resources team in Raheen, Limerick. You will validate methods and equipment for sterility, bioburden, and endotoxin testing, write technical documents, and culture organisms for investigations and development.

The role emphasizes GMP QC laboratory experience, aseptic techniques, and strong problem-solving skills, with opportunities to contribute to regulatory inspections and continuous improvement.

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