Associate Scientist, Bioanalytical Sciences

Regeneron Pharmaceuticals•Tarrytown, GA

2d•$93,900 - $153,300•Onsite

About The Position

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Scientist to join our Bioanalytical Sciences Quality Control team in an on-site capacity. In this role, you will perform quality control review of documentation, building foundational GxP knowledge while beginning to independently interpret findings and solve problems within defined procedures while collaborating with QC management, peers, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

Requirements

Bachelor's or Master's degree and 0-3 years of relevant post-degree experience
Conduct yourself with professionalism and integrity while maintaining a strong work ethic
You communicate clearly and concisely, and you listen actively to understand the needs of your team and stakeholders
You adapt readily to changing priorities in a fast-paced environment
You're invested in your own professional development and welcome giving and receiving feedback
You bring scientific curiosity to your work, asking thoughtful questions to deepen your understanding

Nice To Haves

Foundational knowledge of GxP principles and industry practices/standards is a plus

Responsibilities

Build foundational knowledge of established QC processes by reviewing, verifying, and acknowledging documentation under the direct supervision of management
Assemble available resources to perform QC, learning to evaluate the quality of various forms of documentation
Manage multiple documentation types at once, sharpening your ability to multi-task effectively
Develop foundational problem-solving skills by learning appropriate approaches to resolve findings
Collaborate with and engage stakeholders across functions to improve documentation quality
Participate in QC sub-team and group meetings, sharing the results of your work with others
Provide cross-functional support as needed, broadening your exposure across the organization