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Usp process expert msat

Visp
Lonza
Inserat online seit: 4 Oktober
Beschreibung

Join to apply for the USP Process Expert MSAT role at Lonza

Location: Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Lonza is a global leader in life sciences operating across three continents. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. This role focuses on leading technology transfers and implementing manufacturing processes from design to full-scale production, serving as a key link between development and operations, and contributing to continuous improvement. The position is based in Visp, Switzerland.

Reference: R69263


Key Responsibilities

* Leading cross-functional teams as a process expert tasked with technology transfers (process design and up-scaling) and timely process implementation at manufacturing scale. This includes the whole lifecycle of assigned projects from planning over coordination, implementation, control and project completion aligned with project management goals
* Act as the interface between the process donor (external customer, process development) and operations. Responsible to ensure process scalability and manufacturability
* Securing success during technology transfer by applying formal processes and tools to manage the transfer of information, process related risks and change control
* Responsible for the resolution of process issues that may arise during manufacturing, considering all regulatory requirements. This includes on call duty
* Responsible for execution of GMP risk analysis for the manufacturing processes
* Ensuring timely compilation of process related deviations, change requests and campaign reports as well as responsible for continuous improvement of process performance


Key Requirements

* PhD or equivalent experience (preferred), Master’s/Master’s degree in biotechnology, chemical engineering or related fields
* Working experience in biopharma manufacturing and / or process development preferable in of Mammalian Manufacturing
* Deep understanding of GMP and bioprocess technology
* Very good communication skills and interaction with all kinds of interfaces within customers and the project organization
* Fluency in English


Seniority level

* Not Applicable


Employment type

* Full-time


Job function

* Management and Manufacturing


Industries

* Pharmaceutical Manufacturing
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