Req ID:

R010889

Locations:

Dublin, IE; Belfast, Antrim and Newtownabbey, UK; London, London, City of, UK; US - Home-Based, CA -- [Remote/Home-Based]

Category:

Technical Operations

Brief Description: Reporting into the Senior Director, Drug Substance Development, this role will provide scientific and technical leadership for drug substance development projects at various stages of the development life-cycle. Success requires application of scientific and/or engineering principles and creativity to process design and development studies, and translation into commercially …

Req ID:

R010914

Locations:

Dublin, IE; London, London, City of, UK -- [Remote/Home-Based]

Category:

Technical Operations

Jazz Pharmaceuticals is looking to hire an experienced External Manufacturing Lead (EML) to join our External Manufacturing organisation. The EML will have overall responsibility for the performance of an external Contract Manufacturing Organisation (CMO) portfolio for Drug Substance commercial products. The EML will be required to build and manage strong …

Req ID:

R010990

Locations:

Dublin, IE; Villa Guardia, Roma, IT; London, London, City of, UK -- [Remote/Home-Based]

Category:

Technical Operations

The Global Project & Program Manager (GPPM) will lead cross-functional teams in the management and execution of projects/programs within the Portfolio with minimum supervision, ensuring successful delivery on time, within scope, and within budget. S/He will be responsible for managing full project lifecycles, from project proposal to completion / operational …

Req ID:

R010668

Locations:

Dublin, IE; London, London, City of, UK; Trenton, NJ; Albany, NY; Philadelphia, PA -- [Remote/Home-Based]

Category:

Technical Operations

Brief Description: The Senior Director, Biological Analytical Development is responsible for providing both leadership and hands-on technical expertise for analytical aspects of biologic CMC programs. This role combines strategic oversight with direct scientific contributions ensuring delivery of high-quality methods, specifications, and regulatory documentation to enable clinical development and regulatory submissions. …