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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Quality Assurance Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeEast Greenbush, NY, USA$62.4k - $110k /yr

About the Job

Requirements

  • A Bachelor of Science degree in life sciences or a related field is required; proven experience may substitute for the education requirement.
  • For Associate QA Specialist level, 2 or more years of experience are required.
  • For QA Specialist level, 4 or more years of experience are required.
  • Ability to perform physical requirements for the entirety of a shift of up to 10 hours in a cleanroom environment, including bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation, and lifting, pushing, or pulling up to 50 pounds.
  • Ability to wear full cleanroom attire, which may include laundered undergarments, a gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves, and sanitizing agents during gowning.
  • Ability to remove jewelry, makeup, and nail adornments while wearing cleanroom attire.

Responsibilities

  • Support Quality Assurance initiatives on topics related to the start-up and operations of a drug product facility.
  • Work on and potentially lead efforts to establish new programs, including the start-up of formulation, filling, inspection, assembly, and pack-and-label teams.
  • Assess existing procedures and documents for suitability for drug product operations and identify a path forward for establishing procedures when current documents are inadequate.
  • Develop, write, review, and approve standard operating procedures, specifications, and other documents, including operations and facility procedures, quality training materials, and batch documentation.
  • Maintain project timelines to support evolving business needs.
  • Perform on-the-floor quality reviews of equipment logs, training records, testing results, batch records, and supporting documents.
  • Review and approve electronic and paper-based documents.
  • Provide mentorship during on-the-floor manufacturing.
  • Support audits, inspections, and investigations.
  • Perform material quarantine and segregation, and conduct line clearances.
  • Contribute to continuous-improvement initiatives.
  • Adjust the schedule based on facility start-up, filling, and manufacturing needs.
  • Collaborate with cross-functional internal teams.

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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