Staff Scientist, Analytical Formulation Development

Tarrytown, NY, United States
Sep 10, 2020
Required Education
Associate Degree
Position Type
Full time
We are seeking a Staff Scientist to join our Formulation Development Group in Tarrytown, NY to support key analytical method development and method characterization. Our group drives the development of fit for purpose methods utilized to measure purity and stability of antibody-based drug product formulations and drug product images. These newly created analytical methods we utilize at various stages of clinical and commercial development, including creation and performance qualification of methods to support IV studies. We are looking for someone who will proactively carry out research on protein formulation, protein stability, protein characterization, and innovative analytical technologies.

A Typical Day Might Look Like The Following:

- Developing and qualifying analytical methods to drive formulation development, process development, and stability testing for various programs

- Leading other scientists and research associates in conducting research and developmental activities; Serve as Analytical Team representing in cross functional meetings

- Overcoming challenges related to methods used to assess product quality and stability

- Setting goals, assigning tasks, and providing performance management and development

- Authoring and refining sections of regulatory and technical documents, method SOPs, method performance reports, and method transfer as it bolsters pharmaceutical development

This Role Might Be For You If:

- You can work productively as an independent and within a multi-faceted environment

- You have excellent communication skills in order to share new findings with the team

- You are deeply passionate about science with an interest in drug development and discovery

To be considered for this opportunity, you must have a PhD in analytical chemistry, chemistry, biochemistry, pharmaceutical science, chemical or biomedical engineering or a related field. We would like someone who also possesses at least 3 years of proven experience developing analytical methods for biological drug products and/or characterizing biological drug products. Knowledge and experience in protein stability characterization, degradation pathway identification and particle analysis using biochemical and biophysical tools. A good understanding of ICH guidelines and familiar with analytical requirement for drug product development such as stability study, IV and SC administration is desirable.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!
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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.