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Current job openings

A total of 200 new jobs are expected to be created in connection with the company’s operations over the coming years. Interested candidates can apply for these new Alvotech positions on the company’s website.

New jobs will be created in Iceland
200

Director of Procurement, Alvotech

The Director of Procurement will be responsible for developing and implementing a global outsourcing strategy for all services and procurement at Alvotech.

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Senior Director Project Management (Germany)

Alvotech is seeking a Senior Project Manager with a strong technical product development background in biopharmaceutical R&D, Manufacturing, and clinical development. 

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Senior Biostatistician (Switzerland)

The Senior Biostatistician is responsible to lead and manage all biostatistics related activities on assigned programs/projects including the design, planning and preparation of all Biostatistics and Statistical Reporting deliverables in support of clinical development ...

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Senior Director Project Management (Switzerland)

Alvotech is seeking a Senior Project Manager with a strong technical product development background in biopharmaceutical R&D, Manufacturing, and clinical development.

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Manufacturing Technician - Drug Product Manufacturing (Iceland)

Be able to work in accordance with GMP and EHS practices, conducting all activities in a compliant and safe manner. Performing activities above and beyond their responsibilities as and when required.

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Scientist - Drug Product Manufacturing & Development (Iceland)

Manage the pharmaceutical development aspects of a biosimilar development project as a drug product subject-matter-expert in a cross-functional team.

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System and Network administrator

In this role, you will manage and build up the IT infrastructure for Alvotech, by analysing requirements and installing hardware and software solutions.

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Senior Manager Clinical Supply (Switzerland)

The Senior Manager Clinical Supply will be responsible for the oversight of clinical supply planning and management throughout the lifecycle of all clinical trials sponsored by Alvotech.

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Regulatory Affairs Manager (Switzerland)

As part of multifunctional team, the Regulatory Affairs Manager will be responsible for the operational and logistic aspects for his/her assigned projects and he/she is the primary point of contact for any regulatory related issue, both internally and with external stakeholders. The function is also responsible for adhering to regular planning of tasks in accordance with program timelines, performing the required activities to keep the assigned project(s) on track.

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Clinical Trial Manager (Switzerland)

The Clinical Trial Manager (CTM) will be responsible for the operational and logistic aspects of the assigned clinical trial(s). Within this role, the CTM will be responsible for adhering to regular planning of tasks in accordance with clinical program timelines, performing the required activities to keep the assigned clinical trial(s) on budget, on time and with the highest standard of quality. In addition, the CTM will have to establish day-to-day interactions with the Contract Research Organizations (CROs) and trial sites to ensure sponsor’s oversight responsibilities.

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We always have room for talent

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