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Cryoport Systems

Global temperature-controlled life sciences logistics

Quality Assurance Specialist & Interim Delegated Pharmacist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLouvres, FranceNo salary listedIn-person

About the Job

Requirements

  • A pharmacy diploma and authorization to practice in France are required.
  • Eligibility to perform the duties of an interim delegated pharmacist is required.
  • Registration or eligibility for registration with the French National Order of Pharmacists is required.
  • At least 2 years of experience in the pharmaceutical industry, pharmaceutical logistics, or a biologistics environment, or at least 6 months of quality control experience in a pharmaceutical or biologistics environment, is required.
  • Knowledge of pharmaceutical quality standards and Good Manufacturing Practices is required.
  • Knowledge of Good Distribution Practices is required.
  • Experience in at least one of the following areas is required: biobanks and biological resources; pharmaceutical production; pharmaceutical logistics; biologistics; cell and gene therapies; advanced therapy medicinal products; vaccines; clinical batches; sterile injectable products; mammalian cell culture; immunotherapy; or aseptic pharmaceutical processes.
  • Proficiency with Microsoft Office tools and comfort working in digitalized environments are required.
  • Fluent French and English, both written and spoken, are required.

Responsibilities

  • Participate in deploying and maintaining the site's quality management system.
  • Ensure quality procedures are applied and regularly updated.
  • Contribute to continuous improvement projects for the quality system.
  • Participate actively in developing and evolving quality processes.
  • Ensure activities comply with applicable regulatory requirements and internal standards.
  • Perform quality checks and verify customer orders conform before shipment.
  • Identify, investigate, and monitor quality nonconformities and deviations.
  • Participate in the evaluation and qualification of new equipment.
  • Support operational teams in applying quality and regulatory requirements.
  • Help secure the flows of biological and pharmaceutical products.

Desired Qualifications

  • Experience within a contract development and manufacturing organization is an asset.
  • Knowledge of ISO 9001 requirements is appreciated.

About the Company

Cryoport Systems

Global temperature-controlled life sciences logistics

Cryoport Systems provides global, temperature-controlled supply chain services for life sciences, handling the logistics and storage of critical therapies, vaccines, and materials that must be kept at specific temperatures. Its offering includes end-to-end support for clinical trials and commercial products, ensuring products are kept at the right temperatures from pickup to delivery through specialized packaging, refrigerated storage, and temperature monitoring across a worldwide network. The company differentiates itself by providing an integrated, trusted cold-chain platform that covers multiple stages of the supply chain and is already supporting hundreds of clinical trials and leading therapies. The goal is to help life sciences companies move, store, and deliver irreplaceable products safely and efficiently, enabling patients to receive treatments on time.

Company size
51-200
Company stage
IPO
Headquarters
Brentwood, TN
Founded
1990

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