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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

QA leader - (Germany)

Der Leiter der Qualitätssicherung (m/w) am Standort in Jülich berichtet er / sie direkt an die höchste QA Funktion innerhalb von Alvotech, welche im Headquarter von Reykjavik angesiedelt ist.

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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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Head of Clinical Supply (Switzerland)

The Head of Clinical Supply will be responsible for the oversight of clinical supply planning and management throughout the lifecycle of all clinical trials sponsored by Alvotech. This includes planning and forecasting of clinical trial material, packaging, labeling, shipment and return/destruction of clinical supplies.

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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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Strategic & Relationship Manager – Clinical and R&D (Switzerland)

The RnD Procurement Manager (RnDPM) will be responsible for supporting the operational and logistic aspects within the RnD Organization by optimizing purchase of goods and/or services. Within the role, the RnDPM will be responsible to identify and manage Clinical Research Organizations (CROs), central laboratories and technical external service providers (ESPs) to provide strategic sourcing options for successful trial delivery and to ensure the delivery of quality, timely and cost-effective external resources to support global activities.

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Clinical Project Manager (Switzerland)

The Clinical Project Manager (CPM) will be responsible for the operational and logistic aspects of the assigned clinical program(s). Within this role, the CPM 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 program(s) on budget, on time and with the highest standard of quality.

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Senior Project Manager (m/f - Germany)

The main goal of the PM department at Alvotech is to coordinate internal and external resources, especially subcontractors and partners for process development and analytical services. PM is responsible for the definition and tracking of project milestones, delivering progress reports, the budgeting and controlling of projects, and informing key stakeholders of the status, issues and proposed solutions. PM is a key function involved in the whole life cycle of each product.

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We always have room for talent

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