Manufacturing Operations Consultant

Long-term contract opportunity to work for one of the leading Gene editing companies. They are rapidly translating their specific, efficient and versatile gene-editing platform into therapies to treat a variety of diseases, and require a senior consultant who can interface with Contract Development and Manufacturing Organizations (CDMOs) that are part of their supply chain and primarily oversee activities related to GMP manufacture of their gene edited drug products


The ideal candidate will have:

• Excellent knowledge of cell and gene therapy and/or biologics process development and manufacturing with tech transfer, scale-up and clinical/commercial manufacturing.
• Comprehensive knowledge of GMP, aseptic processing, ATMP requirements
• Has been involved in the development and scale-up of multiple products across different product lines, reflecting a breadth of understanding of cell culture process requirements.
• Experience in working with CDMOs and third parties for process development and cGMP manufacturing.
• BS/MS in Chemical/Biochemical Engineering or related discipline (e.g. Chemistry/Biochemistry), and Sr. Engineer with 5 or more years of industrial experience in the development and manufacturing of biopharmaceuticals for example proteins, vaccines, and/or cell and gene therapy products.

Candidates are currently being shortlisted for interview so if your experience is a good fit for this role and it seems like something you would like to get involved in or hear more about - apply today!

The candidate must have the rights to work in the location stated in the job advert.

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