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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Principal Pathologist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeTarrytown, NY, USA$150.5k - $245.5k /yr

About the Job

Requirements

  • A Doctor of Veterinary Medicine or PhD in Pathology is required.
  • At least 2 years of professional experience relevant to the position is required.
  • Board certification in veterinary anatomic pathology (DACVP or DECVP) is required.

Responsibilities

  • Apply toxicologic pathology expertise to help shape research programs supporting the discovery and development of medicines.
  • Serve as study pathologist for in-house discovery studies and produce pathology reports that inform scientific decision-making and support regulatory submissions.
  • Provide digital or glass-slide pathology peer review for Regeneron toxicology studies conducted at contract research organizations.
  • Use digital image analysis when appropriate to strengthen study interpretation and scientific insight.
  • Contribute to the development of an in-house digital pathology program.
  • Present scientific contributions through internal and external forums supporting regulatory and discovery programs.
  • Contribute to scientific publications, including manuscripts, abstracts, posters, and oral presentations.
  • Participate in seminars, workshops, and conferences to stay connected with the toxicologic pathology community.

Desired Qualifications

  • Experience at a contract research organization is preferred.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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