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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

QC External Lab Coordinator

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRensselaer, NY, USA$25.24 - $39.47 /hr

About the Job

Requirements

  • A bachelor's degree in Biology, Chemistry, Microbiology, or a related scientific field is required.
  • Experience with current Good Manufacturing Practice (cGMP) is preferred.
  • The role may require on-call availability during off-hours, including weekends and holiday breaks, to support critical shipments or entry of results.

Responsibilities

  • Serve as the primary operational liaison between Contract Testing Laboratories and internal partners, including Quality Control, Quality Assurance, Regulatory Affairs, Manufacturing, and Supply Chain teams.
  • Lead cross-functional meetings with Contract Testing Laboratories and internal partners to establish project timelines, discuss technical issues, supervise progress, and drive issue resolution.
  • Monitor Contract Testing Laboratory performance metrics, turnaround times, testing capacity, and schedule adherence; identify growing risks and implement mitigation plans as appropriate.
  • Use a Laboratory Information Management System (LIMS) to review sample inventory against samples sent to and received from external laboratories, resolve discrepancies, and maintain sample integrity.
  • Coordinate activities between external laboratories and internal subject matter experts to troubleshoot issues and identify root causes.
  • Coordinate on-time shipment of samples to Contract Testing Laboratories.
  • Coordinate receipt and entry of test data from Contract Testing Laboratories.
  • Provide technical support for invalid assays, deviations, and out-of-specification/out-of-trend investigations.
  • Initiate and complete corrective and preventive actions (CAPAs) and Change Controls in accordance with site procedures.
  • Write new standard operating procedures (SOPs) and update existing SOPs as needed.
  • Initiate and handle workflows in the electronic document management system.
  • Ensure all work follows applicable regulatory requirements, including cGMP, company policies, and SOPs.
  • Proactively identify and implement process improvements and lean initiatives.
  • Perform other duties relevant to the position as required.

Desired Qualifications

  • Experience with cGMP.

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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