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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Director – Medical Device Quality Assurance

Regulatory & Quality (Life Sciences)Updated on Nov 5
Full-timeEast Greenbush, NY, USA$175.7k - $292.7k /yr

About the Job

Requirements

  • A BS/BA and 12+ years of experience in the medical device or combination product industry, or an equivalent combination of education and experience.
  • Understanding of applicable industry regulations, including 21 CFR Part 4, 21 CFR Part 820, and ISO 13485.
  • Demonstrated knowledge of combination product development requirements, specifically related to Design Controls.
  • Current knowledge and/or experience with quality assurance systems such as CAPA, deviations, investigations, and change control.

Responsibilities

  • Provide Quality Assurance oversight of the Medical Device / Combination Products function.
  • Collaborate across the organization to provide development support.
  • Develop strategies and processes to strengthen the integration of Combination Product development into the organization.
  • Create resource plans to ensure adequate Quality Assurance support of combination product development projects and other projects across the organization.
  • Lead all aspects of the professional development of the Medical Device Quality Assurance team, including managers and engineers.
  • Drive the department toward optimal performance, reducing errors and improving efficiencies.
  • Set goals for the department to align with corporate Quality Assurance goals.
  • Collaborate with internal collaborators, external partners, and agencies.

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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