Formulation & Process Intern: Scale-Up Lab to Pilot

(1206) Opella Healthcare Group SAS

Compiègne

Sur place

EUR 11 000 - 17 000

Plein temps

Il y a 11 jours
Générateur de candidature

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Résumé du poste

Opella Healthcare Group SAS is offering a 6-month internship in Drug Product Development & Delivery at our Compiègne site. The role focuses on formulation and process engineering for optimization and scale-up, including raw materials study and DOE-driven parameter definition.

You will work with formulation and analytical teams to plan pre-formulation studies, produce lab and pilot batches, and ensure quality and safety standards are met. Fluency in French/English is required.

Qualifications

  • Currently pursuing a degree in Engineering, Pharmaceutical or Scientific related fields.
  • Knowledge of process engineering and DOE is desirable.
  • Previous laboratory experience and formulation knowledge are a plus.
  • Analytical and synthesis abilities are valued.
  • Strong communication skills and ability to work collaboratively in a team.

Responsabilités

  • Realize a bibliography study on raw materials and patent landscape.
  • Liaise with raw materials suppliers.
  • Manufacture first pre-formulation studies and define process parameters.
  • Produce laboratory and pilot scale batches for scaling up.
  • Propose DOE and QBD approaches to define and optimize parameters.
  • Study analytical data from compatibility studies and lab batches.
  • Write protocols, batch records and reports for technical trials.
  • Collaborate with R&D teams for formula and process implementation.
  • Ensure compliance with safety and quality standards.

Connaissances

Process engineering
DOE
Lab experience
Analytical skills
Teamwork
French/English

Formation

Engineering/Pharmaceutical degree

Outils

AI tools

Description du poste

Opella Healthcare Group SAS is offering a 6-month internship in Drug Product Development & Delivery at our Compiègne site. The role focuses on formulation and process engineering for optimization and scale-up, including raw materials study and DOE-driven parameter definition.

You will work with formulation and analytical teams to plan pre-formulation studies, produce lab and pilot batches, and ensure quality and safety standards are met. Fluency in French/English is required.

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