9 pharmaceutical jobs found in New York, NY

As Regeneron continues to push the boundaries of science to create life-changing medicines for people with serious diseases worldwide, we're evolving our capabilities to cultivate a culture of safety, environmental stewardship, and compliance. In this newly formed role as Director of Occupational Toxicology, you will provide robust, scientifically-sound hazard analysis, risk profiles, and risk mitigation strategies for novel therapeutics handled in our laboratory, scale-up, and manufacturing settings. Success in this role will require partnering with our EHS teams and key stakeholders across Regeneron to support the evolution of our occupational toxicology programs and business strategies. This role is based at our Corporate Research HQ in Tarrytown, NY and is not open to remote assignments As Director EHS, Occupational Toxicology, a typical day may include: Responsible for development and life cycle management of ADEs, OELs, and SDS documentation, including risk...

We are seeking a Director to join our Clinical Development team. The Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Director leads in a matrix environment as part of a cross-functional team and may contribute to drug-candidate development projects through early and/or late phase development. The Director reports to the Internal Medicine Clinical Development Unit Lead of Clinical Scientists and collaborates closely with Medical Director(s)to provide scientific expertise vital to design and deliver on clinical studies and programs. As a Director, a typical day may include the following: May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist; Member of the Clinical Study Team and Global Clinical Sub Team Contributes to program team meetings,...

Regeneron, located in Tarrytown, NY is seeking an energetic Process Development Engineer I to support technology transfer and business operations in the Technology Transfer & Logistics (TT&L) group within Preclinical Manufacturing and Process Development. In this role, you will lead production process transfer to support preclinical and clinical manufacturing at internal and external sites, as well as manage and coordinate a wide variety of departmental business operations. A Typical Day in This Role Might Look Like: Lead cross-functional teams to complete process transfer and establishment of production processes at internal and external clinical manufacturing facilities, with a focus on early-stage programs. Work to ensure the successful start-up of manufacturing production campaigns. Drive team cooperation to facilitate resolution of cross-functional issues and/or provide value-adding solutions. Ensure effective, accurate and timely communication...

Regeneron is seeking a Process Development Engineer I as a full-time position to work in the Purification Development group within Pre-Clinical Manufacturing and Process Development (PMPD). In this exciting role you will be primarily involved in the design and implementation of viral clearance studies to demonstrate virus safety of biotechnology products throughout the product development cycle from Phase I clinical trials through commercial licensure. A Typical Day in The Role Might Look Like: Design and leads multiple viral clearance projects with supervision Develops and qualifies scale-down models for viral inactivation, chromatography and membrane filtration unit operations Travels to external laboratories (20 – 25%) to execute viral clearance studies in accordance with GLP Collaborates with cross-functional groups to coordinate study logistics Summarizes studies and results in electronic laboratory notebooks, technical reports, and regulatory filings...

Regeneron's Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking an energetic Process Development Engineer II as a full-time position to work in the Purification Development group. In this role, you will accelerate early-stage medicine development and scientific understanding, developing speed-to-clinic processes. This involves developing scalable downstream unit operations through bench and pilot scale experiments to transfer technical process knowledge for manufacturing. A Typical Day in the Role of Process Development Engineer II Might Look Like: Perform process development for clinical processes through bench scale and pilot scale experiments Document experiments, results, and findings in electronic laboratory notebook Maintain instruments and tackle instrumental/experimental problems Development or onboarding of new technology and automation to increase process throughput and efficiency of preclinical...

We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs. As an Associate Director a typical day may include the following: May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist Contributes to program team meetings, scientific advisory boards, study...

Regeneron Pharmaceutical’s Analytical Chemistry Group is seeking a highly motivated Sr. Scientist to join our group. Sr. Scientists work with LC-MS technologies to guide and support development and characterization of therapeutic protein candidates and other modalities. We apply and solid understanding of various LC-MS platforms and applications to solve analytical problems. A Typical Day in the Role of Sr Scientist Might Look Like: Design, complete, and optimally communicate analytical characterization of biotherapeutics, including monoclonal and bispecific antibodies, Fc-fusion proteins, and other modalities (adeno-associated virus, mRNA, siRNA, etc.) to support drug discovery and development. Lead and deliver on characterization activities to elucidate product quality attributes like post-translational modifications, sequence variants, charge variants, size variants, and host cell proteins. Form and maintain inter-departmental collaborations to solve any potential drug...

Our Analytical Chemistry Group (ACG) at Regeneron is seeking a highly motivated Scientist in support of Regeneron R&D programs. In this exciting role, you will work in a mass spectrometry lab and focuses on the biochemical characterization of emerging novel therapeutic modalities as well as therapeutic monoclonal antibodies at all stages of development. A Typical Day In The Role of Scientist Looks Like: Develop primarily LC-MS based analytical methods to support various R&D programs. Perform LC-MS data analysis using various software and bioinformatic tools to elucidate the quality attributes of therapeutic proteins and other novel modalities. Support R&D activities and regulatory applications and deepen our knowledge of antibody therapeutics and other emerging novel modalities. Perform sample preparation and LC-MS-based experiments independently based on SOPs and document experiments, results and findings in electronic laboratory notebook (ELN) entries...

We are seeking an Associate Director within the Formulation Development Group of Regeneron Pharmaceutical Inc. at Tarrytown, NY. This role will lead clinical and commercial formulation and drug product development activities for peptides, monoclonal antibodies (mAb), antibody-drug conjugates (ADC), fixed dose combinations, and combination products. Specialized focus on obesity and metabolic disease. A typical day in this role might look like: Leads clinical and commercial formulation and drug product development activities for peptides, monoclonal antibodies (mAb), antibody-drug conjugates (ADC), fixed dose combinations, and combination products. Specialized focus on obesity and metabolic disease. Applies demonstrated knowledge of risk management and application of QbD principles to formulation and drug product development. Integrates analytical and process development. Interacts broadly and collaboratively with other Regeneron functions and stakeholders including...