Sr Assoc Scientist, Formulation Development

Regeneron's Formulation Development Group (FDG) is seeking a Sr. Associate Scientist who will be planning, optimizing, designing, executing, and documenting Drug Product process development studies, including developing scaled-down models. The candidate will work closely with FDG leads and scientists to support development activities across multiple programs and ensure a seamless technology transfer to the manufacturing team. In addition, the Sr. Associate Scientist will also support full functionality and maintenance of the state-of-the-art process development facility, including procurement, installation, maintenance, training, and equipment operation.

A Typical Day In The Role Might Look Like

• Manage equipment installation, operation, maintenance, calibration, and repairs.
• Work closely with key members of formulation development and facility management teams to ensure full functionality of Drug Product Pilot Facility (DPPF).
• Conduct filling campaigns to support toxicological studies, equipment commissioning, and related activities.
• Procure consumables and continuously update the inventory for the DPPF.
• Independently design and execute Drug Product (DP) process development activities for different unit operations across multiple programs.
• Assist in developing small scale models to effectively mimic manufacturing unit operations and support technology transfer to manufacturing teams.
• Work very closely with FDG leads/scientists to ensure seamless progression of multiple late-stage process-related activities.
• Able to effectively engage with others and work in cross-functional teams to support process development.
• Communicate relevant information in a clear and transparent manner, and effectively collect information through strong listening skills.
• Bring in new ideas from literature or external practices, and engage in active questioning to understand context and interpretation of work.
• Demonstrate strong problem-solving skills.
• Prepare, review, and edit technical reports.
• Comfortably shift gears and priorities to meet changing business needs as required.
  
  
  

This Job Might Be For You If

• You have strong initiative and drive to complete challenging tasks and learn new technologies.
• You are capable of multi-tasking, working both independently and within a team environment.
  
  
  

This position requires a BS degree in Biomedical or Chemical Engineering, Pharmaceutical Sciences, or related field with at least 1 - 3 years of relevant industry experience. Experience with Drug Product (formulation and process) development and characterization. Solid understanding of analytical instruments used for protein therapeutics characterization, such as HPLC-based chromatographic techniques (icIEF, SEC, IEX), biophysical methods (DLS, DSC, and UV-Vis), and particle characterization methods (MFI and HIAC). Prior research experience in the areas of protein structure, stability, and protein aggregation. Basic understanding of common protein degradation pathways. Ability to work independently or in a team setting; strong problem-solving skills; quickly adapt to change to support accelerated timelines; efficient time management. Experience with coding and statistical software is a plus (JMP, R).

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible 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 parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$79,100.00 - $129,100.00