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Sanofi

Global pharma company; vaccines and R&D

Quality Control Microbiology Testing

Inspection & TestConfirmed live in the last 24 hours
Full-timePearl River, NY, USA$69k - $99.7kIn-person

About the Job

Requirements

  • Bachelor's degree in Life Sciences, Biology, Chemistry, or a related field.
  • At least 1 year of laboratory or manufacturing experience.

Responsibilities

  • Execute analytical testing in a timely manner and adhere to committed schedules.
  • Perform tasks according to current good manufacturing practice (cGMP) and health, safety, and environment (HSE) requirements, including associated instructions, procedures, and records.
  • Record all required raw data, calculations, and task-related information in compliance with cGMP and data integrity requirements.
  • Maintain training and qualification to perform assigned analytical testing on various samples, including raw materials, in-process drug substance samples, and environmental monitoring samples.
  • Review quality control (QC) data from tests performed by other analysts, as delegated by management, and meet committed schedules.
  • Inform the manager promptly of quality or HSE events, including deviations and out-of-specification events, so investigations and impact assessments can be completed appropriately.
  • Participate in investigations in which the employee is involved, supporting appropriate investigation and impact assessment.
  • Execute assigned corrective and preventive actions (CAPAs) related to remediation plans and continuous improvements.
  • Maintain the laboratory, facilities, and instruments in a suitable quality and safety condition.
  • Build remediation plans related to inspection-readiness gaps, findings, and deviations.
  • Contribute to trending environmental monitoring and utilities monitoring data, and assist with or author periodic reports as needed.
  • Train team members in analytical testing and documentation after qualifying as a trainer, ensuring adherence to local and global standard operating procedures and cGMP requirements.
  • Keep the laboratory audit-ready and represent the laboratory team during audits and inspections.
  • Revise and update local procedures as needed to align with cGMP and current good laboratory practice (cGLP) guidelines and improve usability for laboratory activities.

Desired Qualifications

  • Experience in a pharmaceutical or related industrial environment.

About the Company

Sanofi

Global pharma company; vaccines and R&D

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company size
10,001+
Company stage
IPO
Headquarters
Paris, France
Founded
1973

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