Process Development Associate II - PreClinical Manuf. and Process Dev

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.

Summary

This position could support any of the groups across our Pre-Clinical Manufacturing and Process Development effort.
The various subgroups within the department are as follows:

• Cell Culture Development: Screen and identify top tier candidate biologics, select cell lines, develop new methodologies and processes for cell line medium and feed, and optimize cell culture processes for clinical and commercial manufacturing products. Includes supporting technology transfer to GMP manufacturing.

• Bioreactor Scale-Up and Development: Cultivate mammalian cells for production of biologics using bench and pilot scale bioreactors, characterize scalability of clinical and commercial processes, analyze data, troubleshoot processes and equipment, develop process controls. Includes supporting technology transfers to GMP manufacturing.

• Purification Development: Design, optimize, and characterize purification strategies for biologic medicines from preclinical through licensure. Includes supporting technology transfer to GMP manufacturing.

• Process Development Analytics: Positions in process analytics team focus on the development, optimization and running of assays that support characterization of pre-clinical and clinical processes for both upstream (cell culture & medium development) and downstream (purification) functions.

• Technology Transfer & Logistics: Using project management tools and techniques, coordinate and optimize departmental business operations within PMPD and with other customers throughout REGN. Lead process transfers of clinical protein candidates to our clinical and commercial production teams, provide financial forecasting & data analyses to identify resource constraints and optimization.

Requirements
Preclinical Manufacturing and Process Development is seeking candidates with a minimum of a BS (MS welcome to apply) in Chemical Engineering, Biochemical Engineering, Bioengineering, Biotechnology /Biochemistry, GPA of at least 3.0; 3.4 preferred. Use knowledge and experience to solve problems and promote the exchange of ideas and knowledge in all directions. Applicant should exhibit analytical and critical thinking, ability to work effectively within a team environment, and comfort working within tight or rapidly evolving timelines are all part of the job.

This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.

To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.