QC Microbiology Scientist Full-time

QC Technical Resources Specialist

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & Where:

Location: Raheen, Limerick

What You'll Do:

• Supporting assay development/validation activities for the QC group from method readiness through to validation.
• Ensuring the operational readiness through management of sample / material requests.
• Coordinating analytical assay transfer internally and externally.
• Reviewing analytical development reports, assay and process validation reports and other technical documents for technical correctness and regulatory compliance.
• Communication of method updates to partners and tracks progress of updates.
• Coordinating multi-site trending and reviews and communicates information as needed to subject matter experts.
• Supporting method Lifecycle activities including method performance reporting, quality metrics and project timelines.
• Tracking team activities and timelines to ensure that the deliverables within the project plans are met and are on-time.
• Communication to management for validation/transfer timelines.
• Continuously driving to improve processes for improved performance.

The Environment and Physical Rhythms of This Role:

• Strong ability to work independently and part of a global team.
• Proficient with the Microsoft suite and project management tools.
• Effective time management.
• Excellent written and verbal communication skills.
• Ability to develop strategies and metrics to measure effectiveness.
• Identifying and effectively communicating risks.

Let's Find Out If We're a Fit:

• Associate Specialist: Requires BS/BA in a life sciences (or related) field and 0-2 years experience or equivalent combination of education and experience.
• Specialist: Requires BS/BA in a life sciences (or related) field and at least 2 years of relevant experience in a cGMP environment or equivalent combination of education and experience.
• Senior Specialist: Requires BS/BA/MSc in a life sciences (or related) field and 4-5 years of relevant experience in a cGMP environment or equivalent combination of education and experience.

Thrive Today. Grow Tomorrow.