Associate Scientist, Product Biochemistry

The Product Biochemistry group is seeking a highly motivated Associate Scientist to support the in‑depth biochemical and biophysical characterization of biotherapeutic molecules. The successful candidate will contribute to method development, assay support, and technology innovation efforts that advance research, pre‑clinical, and clinical programs.

This role involves close collaboration with cross‑functional teams and supports programs from early‑stage research to post-commercial activities. This role will primarily focus on GxP characterization and stability testing of reference standards.

As an Associate Scientist, a typical day may include: Perform biochemical and biophysical characterization experiments to assess quality attributes of protein- and/or oligonucleotide‑based therapeutics using techniques such as capillary electrophoresis, size exclusion chromatography coupled to multi-angle light scattering (SEC-MALS), dynamic light scattering (DLS), fourier transform infrared spectroscopy (FT-IR), fluorescence spectroscopy, circular dichroism (CD), differential scanning fluorimetry (DSF), and general lab techniques (pH, analytical balance, sample preparation).

Develop, optimize, and run light scattering–based assays (e.g., SEC-MALS, DLS, and related methods) with manager guidance to support molecule characterization and method qualification. Analyze and interpret experimental data; identify trends and communicate key findings to project teams.

Accurately document all laboratory activities, data, and analyses in electronic laboratory notebooks (ELN) in accordance with established procedures. Oversee and maintain GxP lab equipment in adherence with quality assurance (QA) standards.

Writing SOPs, summary of analysis (SoA’s), reports and recording information in a GxP controlled environment Prepare clear, well‑organized summaries of results (figures, tables, graphs) for presentations, reports, and regulatory‑supporting documentation.

Present experimental results at group, departmental, and cross‑functional meetings. Maintain, troubleshoot, and operate essential laboratory instrumentation; ensure readiness of equipment and supplies. Follow laboratory safety practices and contribute to an organized, compliant lab environment.

This role may be for you if: You enjoy working in a fast-paced environment You are a fast learner and have desire to expand your skill set and learn new techniques You are detail oriented, well-organized and can multi-task You are a team player You have strong communication skills To be considered, you must have the following: Hands‑on experience with general laboratory operations and data organization, working under managerial supervision.

Fundamental technical proficiency in analytical methodologies such as: Size Exclusion Chromatography (SEC), UV‑Vis spectrophotometry, spectroscopic-based methods (i.e., CD and FT-IR) Understanding of biochemical and biophysical characterization principles for proteins and/or oligonucleotides.

Strong organizational skills with the ability to prioritize multiple tasks while keeping up with proper documentation Clear written and verbal communication skills; ability to work both independently and collaboratively. Scientific curiosity, attention to detail, and a willingness to learn new techniques and technologies.

Preferred Qualifications Experience with additional analytical platforms such as HPLC/UPLC, light scattering (e.g., SEC-MALS, DLS), CD spectroscopy, fluorescence, FT-IR, and DSF. Exposure to analytical method development and assay optimization.

Familiarity with late‑stage development, comparability, or regulatory‑supporting studies. Experience working in a GxP lab and following SOP’s. Experience with writing technical documents (e.g., SOP’s). Education and Experience Bachelor’s degree in Biochemistry, Biophysics, Chemical Engineering, Biomedical Engineering, or a related scientific discipline with approximately 0 - 5 years of post-degree laboratory experience, or Master’s degree in Biochemistry, Biophysics, Chemical Engineering, Biomedical Engineering, or a related scientific discipline with approximately 0 - 3 years of post-degree laboratory experience.

Physical and Work Environment Laboratory‑based roles require routine standing, sitting, handling laboratory equipment, and lifting light to moderate weights. May involve exposure to common laboratory chemicals and instrumentation in a regulated research environment.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate.

The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process.

If you have any questions, please speak with your recruiter. Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position. Salary Range (annually) $70,300.00 - $110,100.00