Cell & Gene Therapy Process Development Engineer

Institut Curie - Research Center; France; Sur place; EUR 43 000 - 56 000; Plein temps

Avantages offerts par ce poste

Company cafeteria

Public transport subsidy

Company health insurance

Résumé du poste

The Curie Institute Research Center in France seeks a skilled scientist to join the Process Development group at CellAction, focusing on manufacturing processes for cell- and gene-based therapies and ensuring translational feasibility under GMP.

You will develop and optimize processes, transfer pre-GMP workflows into robust, reproducible methods, and create analytical assays to monitor CPPs and CQAs while collaborating across disciplines. Fluent English is required; French is a plus.

Qualifications

• Master’s degree or PhD in Biotechnology, Biochemical Engineering, or related field.
• 2–5 years of experience in process development (cell therapy, gene therapy, or drug development).
• Excellent written and verbal communication skills and ability to present technical information to multidisciplinary teams.
• Knowledge of GMP environment and regulatory expectations.

Responsabilités

• Develop and optimize manufacturing processes for cell and gene therapies, including viral/non-viral vectors and genome editing.
• Transfer pre-GMP processes into robust, reproducible workflows suitable for clinical manufacturing.
• Develop analytical methods and monitor CPPs and CQAs to ensure product quality.
• Collaborate with multidisciplinary teams, troubleshoot, and support continuous process improvement.
• Prepare technical documentation and ensure compliance with GMP and regulatory requirements.

Connaissances

Aseptic mammalian cell culture

Flow cytometry

CRISPR-Cas

Analytical characterization

Good communication

Formation

Master’s degree or PhD in Biotechnology, Biochemical Engineering, or related field

Description du poste

The Curie Institute Research Center in France seeks a skilled scientist to join the Process Development group at CellAction, focusing on manufacturing processes for cell- and gene-based therapies and ensuring translational feasibility under GMP.

You will develop and optimize processes, transfer pre-GMP workflows into robust, reproducible methods, and create analytical assays to monitor CPPs and CQAs while collaborating across disciplines. Fluent English is required; French is a plus.