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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Quality Assurance Specialist - On the Floor

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRensselaer, NY, USA$67.4k - $128.7k /yr

About the Job

Requirements

  • A Bachelor of Science or Bachelor of Arts degree in Life Sciences, Engineering, or a related field, or an equivalent combination of education and experience.
  • Senior QA Specialist level requires 6 or more years of relevant experience; QA Specialist level requires 2 or more years of relevant experience. The level will be determined based on experience.
  • Experience with drug substance.
  • Ability to wear full cleanroom attire, including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves, and use sanitizing agents such as IPA during gowning.
  • Ability to remove jewelry, make-up, and nail adornments when wearing cleanroom attire.

Responsibilities

  • Perform and lead on-the-floor activities supporting disposition of product and/or raw materials while ensuring compliance with Quality Assurance policies and procedures, current Good Manufacturing Practices, standard operating procedures, and Regeneron Standard Requirement Documents.
  • Represent Quality Assurance in complex or significant deviations, change controls, corrective and preventive actions, and related matters, including participating in investigations, evaluations, and problem resolution.
  • Represent the organization on behalf of Quality Assurance with external partners to communicate policies and procedures, liaise with partners, and provide input on regulatory communication.
  • Train and mentor employees by providing process and procedure education and conveying Quality Assurance organizational expectations.
  • Maintain a continuous on-the-floor presence and provide stakeholders with Quality Assurance guidance on events and questions in alignment with applicable policies.
  • Perform activities associated with product disposition, including manufacturing-record review, document review, and source-data review.
  • Review, edit, or approve controlled documents.
  • Review and approve investigations associated with products or processes.
  • Evaluate processes and procedures for continuous improvement.
  • Supervise direct reports.
  • Participate in employee training to ensure requirements are met.
  • Conduct at least monthly performance-feedback meetings with direct reports.

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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