QC Analyst, Drug Product – GMP Release & Data

Regeneron

Limerick

On-site

EUR 25,000 - 40,000

Full time

14 days+
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Job summary

Regeneron in Raheen, Limerick, Ireland is seeking a QC Analyst (Drug Product) to join the QC Chemistry, Drug Product Testing team. The role supports testing and release of biopharmaceutical products for commercial and clinical programs.

The position requires a BS/BA in Life Sciences or related field and a minimum of 2 years of industry experience in a GMP-regulated laboratory. You’ll work in a fast-paced environment focused on quality, compliance, and continuous improvement.

Qualifications

  • BS/BA in Life Sciences or related field.
  • QC Analyst: minimum of 2 years of relevant industry experience.
  • Experience reviewing analytical testing in a GMP-regulated laboratory.
  • Strong organizational and teamwork skills with a commitment to quality.

Responsibilities

  • Perform testing to support product release and stability programs.
  • Review testing documentation to ensure GMP compliance and quality standards.
  • Support validation, qualification, and transfer of analytical test methods.
  • Investigate laboratory events with cross-functional teams.
  • Write and maintain SOPs and test procedures.
  • Complete required trainings and maintain compliance.
  • Manage laboratory supplies for routine operations.
  • Support continuous improvement initiatives in the lab.

Skills

QC testing
GMP compliance
Documentation review
Analytical method transfer
Cross-functional collaboration
Training compliance
Problem solving
Attention to detail

Education

BS/BA in Life Sciences or related field

Job description

Regeneron in Raheen, Limerick, Ireland is seeking a QC Analyst (Drug Product) to join the QC Chemistry, Drug Product Testing team. The role supports testing and release of biopharmaceutical products for commercial and clinical programs.

The position requires a BS/BA in Life Sciences or related field and a minimum of 2 years of industry experience in a GMP-regulated laboratory. You’ll work in a fast-paced environment focused on quality, compliance, and continuous improvement.

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