MedinCell® is a pharmaceutical company at commercial stage that develops innovative long-acting injectable medicines in many therapeutic areas based on our BEPO® technology.
We are looking for a Process DevelopmentEngineer to join our Process Development and Manufacturing team which main mission is to scale-up formulation until manufacturing process intended for clinical batches.
Deploy process and technology transfer for manufacturing of injectable formulations through scale-up to GMP clinical stage Contract Development & Manufacturing Organizations (CDMOs).
Assure the traceability of the data to ensure their integrity and their auditability.
Highlights appropriate resources to support the management of process equipment included maintenance and to ensure relevant training to the leader.
Minimum of 5 years of experience in process development, engineering, technology transfer, scale-up and GMP clinical manufacturing of liquid sterile injectable drug products.
Minimum of a Master’s degree in chemical engineering, process engineering and development or similar.
French and Fluent in English, spoken and written ability to attend complex meetings and write clear reports.
Strong knowledge in regulatory requirements, pharmaceutical guidelines, and international standards, mainly in injectable products. Medincell 34 Autre(s) Stage 0 mois
