QC Resources & Method Transfer Specialist

Initial Therapeutics, Inc.; Ireland; On-site; EUR 37,000 - 88,400; Full time

Job summary

Regeneron seeks a QC Technical Resources Specialist to support assay development and validation within the QC group. The role involves coordinating transfers, managing sample requests, and ensuring regulatory compliance across multiple sites.

Strong independence and teamwork are required, with proficiency in MS Office and project management tools. The position is based in Raheen, Limerick, and salary ranges are provided as a guide for annual compensation.

Qualifications

• BS/BA in life sciences or related field with relevant experience in a cGMP environment.
• 4-5 years of relevant cGMP experience for Senior Specialist.
• MSc preferred for Senior Specialist; ability to work independently in a global team.

Responsibilities

• Support assay development/validation from readiness to validation.
• Manage sample/material requests to ensure operational readiness.
• Coordinate analytical assay transfer internally and externally.
• Review analytical development and validation reports for technical correctness and regulatory compliance.
• Communicate method updates to partners and track progress.

Skills

MS Office

Project management

Independence

Education

BS/BA in life sciences

MSc in life sciences

Tools

cGMP

Job description

Regeneron seeks a QC Technical Resources Specialist to support assay development and validation within the QC group. The role involves coordinating transfers, managing sample requests, and ensuring regulatory compliance across multiple sites.

Strong independence and teamwork are required, with proficiency in MS Office and project management tools. The position is based in Raheen, Limerick, and salary ranges are provided as a guide for annual compensation.