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Pierre Fabre

Allogeneic cell therapies development and commercialization

Quality Assurance, Qualification and Validation Intern

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

About the Job

Requirements

  • The candidate must be preparing a diploma at bac +5 level.
  • The candidate must have strong Microsoft Office skills.
  • The candidate should demonstrate responsiveness and anticipation, adaptability, versatility, and teamwork.

Responsibilities

  • Assist the Quality Assurance Manager in the Qualification and Validation service at the Gien site.
  • Participate in qualification of new equipment, such as a coating turbine.
  • Write the associated documentation for new equipment qualification.
  • Carry out tests associated with new equipment qualification.
  • Define the qualification strategy for transfers of paste products between packaging lines.
  • Write the associated documentation for product-transfer qualification.
  • Carry out tests associated with product-transfer qualification.
  • Participate in daily service activities, including maintaining the qualified and validated status of systems.

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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