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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Quality Control Supervisor

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRensselaer, NY, USA$78.7k - $128.7k /yr

About the Job

Requirements

  • Requires a Bachelor of Science or Bachelor of Arts in Life Sciences or a related field, with a Master of Science preferred, and 5+ years of progressive, relevant experience, preferably in the pharmaceutical or biotechnology industry; equivalent combinations of education and experience are accepted.
  • Supervisory or leadership experience is required.
  • Prior management or supervisory experience is identified as a desired qualification.
  • Experience working in a good manufacturing practice (GMP) environment is identified as a desired qualification.
  • Ability to manage multiple assignments and shifting priorities using organizational and project-management skills.
  • Strong attention to detail and prioritization skills.
  • Ability to communicate clearly and effectively with direct reports, peers, and leadership.

Responsibilities

  • Provide front-line support for laboratory activities, including testing and release of drug product packaging and medical device components.
  • Supervise QC staff, distribute workload, and monitor progress.
  • Review study protocols and reports.
  • Attend meetings to stay informed about development and manufacturing priorities and activities.
  • Ensure compliance with applicable current good manufacturing practice (cGMP) regulations and standard operating procedures (SOPs).
  • Organize laboratory investigations and assay troubleshooting as necessary.
  • Perform personnel-management functions, including timesheet submissions, vacation scheduling, personnel development, and performance evaluations.
  • Write and revise SOPs, methods, protocols, and reports.
  • Oversee daily operations of activities in the area.
  • Support internal and regulatory audits.
  • Ensure personnel receive proper and timely training.
  • Ensure safety standards are maintained.

Desired Qualifications

  • A Master of Science degree is preferred.
  • Relevant experience in the pharmaceutical or biotechnology industry is preferred.
  • Prior management or supervisory experience is desired.
  • Experience working in a GMP environment is desired.

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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