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Pierre Fabre

Allogeneic cell therapies development and commercialization

Expert Quality Intern

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Internship · Winter 2027Castres, FranceNo salary listed

About the Job

Requirements

  • The candidate must be preparing a Bac+5 qualification: a scientific Master's degree specializing in Quality, engineering-school training, pharmacy-faculty training specializing in Quality, or equivalent training.
  • An ability to analyze and synthesize information is desirable.
  • An ability to communicate orally is desirable.
  • Interest in quality systems and digital transformation is desirable.

Responsibilities

  • Participate in implementing and monitoring deployment of the tool's quality-event management module, including deviations, CAPA, and changes.
  • Support users in adopting the new processes and tools.
  • Contribute to preparing training sessions and support materials.
  • Collect and analyze feedback from Operations users and deploy necessary improvement actions.
  • Contribute to deploying performance indicators related to the implemented processes.

Desired Qualifications

  • An ability to analyze and synthesize information.
  • An ability to communicate orally.
  • Initiative and an interest in teamwork.
  • Interest in quality systems and digital transformation.

About the Company

Pierre Fabre

Allogeneic cell therapies development and commercialization

Pierre Fabre Pharmaceuticals (US) develops and commercializes allogeneic cell therapies for oncology and rare diseases. It focuses on bringing next-generation, donor-derived cell therapies to patients with high unmet medical needs and deepens partnerships with biotech companies to advance products through clinical manufacturing and distribution in the US.

Company size
5,001-10,000
Company stage
Seed
Total funding
$13.8M
Headquarters
Toulouse, France
Founded
1951

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