Alvotech er fjölþjóðlegt hátæknifyrirtæki í fremstu röð. Meira en 1400 starfsfólk af um 70 þjóðernum sameinast um að móta framtíðina á sviði líftæknilyfja og tryggja sjúklingum um allan heim betra aðgengi að hágæða lyfjum. Meðal starfsfólks eru margir af færustu vísindamönnum landsins.

Við leyfum fjölbreytileika, forvitni og frumkvæði starfsfólks að njóta sín. Við bjóðum aðlaðandi starfsumhverfi í stöðugri mótun og ögrandi verkefni. Alvotech tryggir að jafnrétti kynjanna til launa og frama nái til alls starfsfólks, hérlendis jafnt sem erlendis. Við viljum laða að okkur færasta fólkið á hverju sviði, án tillits til uppruna eða kyns. Með þessum hætti getum við best þjónað hagsmunum sjúklinga og samstarfsaðilum okkar. 

Vertu með okkur í að bæta lífsgæði fólks og auka aðgengi að hagkvæmum líftæknilyfjum. 


1001-5000

Meginmarkmið jafnlaunavottunar er að vinna gegn kynbundnum launamun og stuðla að jafnrétti kynjanna á vinnumarkaði.

Jafnlaunavottun

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Overview of role: 
Are you passionate about driving process excellence in biopharmaceutical manufacturing? Alvotech is seeking an MSAT Specialist to lead technology transfer, scale-up, and process optimization activities, ensuring seamless transition from development to GMP manufacturing. This role plays a critical part in supporting manufacturing performance, resolving technical challenges, and enabling successful product delivery through strong cross-functional collaboration and technical expertise.
 Key Responsibilities: 
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Lead and manage projects independently or collaboratively, supporting technology transfer, process performance qualification (PPQ), late-stage continuous process monitoring, and lifecycle management.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Provide technical leadership by guiding teams through deviation investigations, ensuring effective root cause analysis, and supporting critical decision-making.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Drive successful transfer of development and manufacturing processes from internal sites to large-scale GMP manufacturing at Alvotech Iceland.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Develop and author comprehensive scale-up strategies prior to technology transfer for both clinical and commercial manufacturing, across internal and external sites.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Oversee the introduction and qualification of new processes into cGMP manufacturing, proactively managing technical risks and ensuring effective cross-functional communication for successful technology transfer outcomes.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Lead investigations into manufacturing deviations, identify root causes, and define appropriate CAPA (Corrective and Preventive Actions).
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Deliver independent on-plant technical support, including process monitoring and advanced data analysis, proactively identifying and mitigating potential risks.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Represent MSAT in complex internal and external project teams, fostering strong collaboration, effective communication, and timely problem resolution.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Drive process optimization and continuous improvement initiatives, leading cross-functional teams to implement enhancements aligned with business needs.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Influence project teams using technical expertise to ensure timely delivery in accordance with business objectives.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Anticipate, evaluate, and resolve technical challenges within area of expertise proactively.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Support technology transfer to CMO (Contract Manufacturing Organization) sites by reviewing documentation, identifying gaps, and maintaining a high level of professionalism during interactions.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Conduct batch reviews and apply continual process learning to resolve gaps and improve unit operations independently.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Stay informed of advancements in biopharmaceutical manufacturing technologies and evaluate their applicability for process innovation, cost reduction, and yield improvement.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Mentor and coach new team members, contributing to a highly skilled, engaged, and collaborative DSP team.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Participate in regulatory review activities and provide timely technical support for product approval processes.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Support process validation strategies and execution.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Develop and review SOPs (Standard Operating Procedures) and Process Description Documents (PDDs), ensuring effective transfer of knowledge to execution teams.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ensure strict compliance with cGMP and EHS standards, performing all activities safely and in alignment with regulatory and company requirements.
&middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Demonstrate strong accountability, professionalism, and the ability to take on additional responsibilities with minimal supervision while adhering to company values and conduct standards.
Qualifications: 
<ul>
<li>Master of Science in Biotechnology or related field.</li>
<li>Knowledge of data analysis tools such as JMP and Minitab etc</li>
<li>Minimum 7-9 years of experience in the biopharmaceutical industry, with a focus on downstream processing (process development, manufacturing, or MSAT).</li>
<li>Strong expertise in industrial biotechnology and monoclonal antibody manufacturing.</li>
<li>Solid understanding of GMP environments and regulatory expectations. </li>
</ul>
What we offer: 
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>

Alvotech hf


Overview of role: 

Are you passionate about driving process excellence in biopharmaceutical manufacturing? Alvotech is seeking an MSAT Specialist to lead technology transfer, scale-up, and process optimization activities, ensuring seamless transition from development to GMP manufacturing. This role plays a critical part in supporting manufacturing performance, resolving technical challenges, and enabling successful product delivery through strong cross-functional collaboration and technical expertise.


Key Responsibilities: 

·






 Lead and manage projects independently or collaboratively, supporting technology transfer, process performance qualification (PPQ), late-stage continuous process monitoring, and lifecycle management.

·






 Provide technical leadership by guiding teams through deviation investigations, ensuring effective root cause analysis, and supporting critical decision-making.

·






 Drive successful transfer of development and manufacturing processes from internal sites to large-scale GMP manufacturing at Alvotech Iceland.

·






 Develop and author comprehensive scale-up strategies prior to technology transfer for both clinical and commercial manufacturing, across internal and external sites.

·






 Oversee the introduction and qualification of new processes into cGMP manufacturing, proactively managing technical risks and ensuring effective cross-functional communication for successful technology transfer outcomes.

·






 Lead investigations into manufacturing deviations, identify root causes, and define appropriate CAPA (Corrective and Preventive Actions).

·






 Deliver independent on-plant technical support, including process monitoring and advanced data analysis, proactively identifying and mitigating potential risks.

·






 Represent MSAT in complex internal and external project teams, fostering strong collaboration, effective communication, and timely problem resolution.

·






 Drive process optimization and continuous improvement initiatives, leading cross-functional teams to implement enhancements aligned with business needs.

·






 Influence project teams using technical expertise to ensure timely delivery in accordance with business objectives.

·






 Anticipate, evaluate, and resolve technical challenges within area of expertise proactively.

·






 Support technology transfer to CMO (Contract Manufacturing Organization) sites by reviewing documentation, identifying gaps, and maintaining a high level of professionalism during interactions.

·






 Conduct batch reviews and apply continual process learning to resolve gaps and improve unit operations independently.

·






 Stay informed of advancements in biopharmaceutical manufacturing technologies and evaluate their applicability for process innovation, cost reduction, and yield improvement.

·






 Mentor and coach new team members, contributing to a highly skilled, engaged, and collaborative DSP team.

·






 Participate in regulatory review activities and provide timely technical support for product approval processes.

·






 Support process validation strategies and execution.

·






 Develop and review SOPs (Standard Operating Procedures) and Process Description Documents (PDDs), ensuring effective transfer of knowledge to execution teams.

·






 Ensure strict compliance with cGMP and EHS standards, performing all activities safely and in alignment with regulatory and company requirements.

·






 Demonstrate strong accountability, professionalism, and the ability to take on additional responsibilities with minimal supervision while adhering to company values and conduct standards.

Qualifications: 


 - Master of Science in Biotechnology or related field.

 - Knowledge of data analysis tools such as JMP and Minitab etc

 - Minimum 7-9 years of experience in the biopharmaceutical industry, with a focus on downstream processing (process development, manufacturing, or MSAT).

 - Strong expertise in industrial biotechnology and monoclonal antibody manufacturing.

 - Solid understanding of GMP environments and regulatory expectations.



What we offer: 


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.




Active

Principal Specialist, DSP MSAT

Overview of role:&nbsp; Are you passionate about downstream processing and ready to make a real impact in biopharmaceutical manufacturing? Alvotech is seeking a DSP MSAT Senior Specialist to support the successful transfer, optimization, and performance of biologics manufacturing processes at our state-of-the-art facility in Iceland.
 Key Responsibilities:
<ul>
<li>Lead downstream process technology transfer and scale-up from development to GMP manufacturing (internal and external sites)</li>
<li>Develop and execute scale-up strategies for clinical and commercial manufacturing</li>
<li>Perform gap assessments and facility fit evaluations for external CMOs</li>
<li>Drive process implementation and qualification into cGMP manufacturing environments</li>
<li>Provide on-plant technical support, process monitoring, and proactive troubleshooting</li>
<li>Lead deviation investigations, root cause analysis, and CAPA implementation</li>
<li>Perform advanced data analysis to ensure process robustness and anticipate risks</li>
<li>Represent MSAT in cross-functional and external project teams, ensuring alignment and delivery</li>
<li>Lead process optimization and continuous improvement initiatives</li>
<li>Influence project teams to ensure timely delivery of technical milestones</li>
<li>Proactively identify and resolve technical challenges within downstream processes</li>
<li>Drive continuous process learning and knowledge capture through batch review and data insights</li>
</ul>
&nbsp;
Qualifications:
<ul>
<li>Master of Science in Biotechnology or related field.</li>
<li>Knowledge of data analysis tools such as JMP and Minitab etc</li>
<li>Minimum 3 years of experience in the biopharmaceutical industry, with a focus on downstream processing (process development, manufacturing, or MSAT).</li>
<li>Strong expertise in industrial biotechnology and monoclonal antibody manufacturing.</li>
<li>Solid understanding of GMP environments and regulatory expectations.</li>
</ul>
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.
If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.
If you have any technical issues, please contact: hr@alvotech.com


Overview of role:


Are you passionate about downstream processing and ready to make a real impact in biopharmaceutical manufacturing? Alvotech is seeking a DSP MSAT Senior Specialist to support the successful transfer, optimization, and performance of biologics manufacturing processes at our state-of-the-art facility in Iceland.


Key Responsibilities:


 - Lead downstream process technology transfer and scale-up from development to GMP manufacturing (internal and external sites)

 - Develop and execute scale-up strategies for clinical and commercial manufacturing

 - Perform gap assessments and facility fit evaluations for external CMOs

 - Drive process implementation and qualification into cGMP manufacturing environments

 - Provide on-plant technical support, process monitoring, and proactive troubleshooting

 - Lead deviation investigations, root cause analysis, and CAPA implementation

 - Perform advanced data analysis to ensure process robustness and anticipate risks

 - Represent MSAT in cross-functional and external project teams, ensuring alignment and delivery

 - Lead process optimization and continuous improvement initiatives

 - Influence project teams to ensure timely delivery of technical milestones

 - Proactively identify and resolve technical challenges within downstream processes

 - Drive continuous process learning and knowledge capture through batch review and data insights





Qualifications:


 - Master of Science in Biotechnology or related field.

 - Knowledge of data analysis tools such as JMP and Minitab etc

 - Minimum 3 years of experience in the biopharmaceutical industry, with a focus on downstream processing (process development, manufacturing, or MSAT).

 - Strong expertise in industrial biotechnology and monoclonal antibody manufacturing.

 - Solid understanding of GMP environments and regulatory expectations.


What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.


About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.

We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.

Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com



Senior Specialist, Manufacturing Operations

Gakktu til li&eth;s vi&eth; framlei&eth;sluteymi&eth; hj&aacute; Alvotech &iacute; Reykjav&iacute;k! Vi&eth; leitum a&eth; einstaklingum me&eth; j&aacute;kv&aelig;tt vi&eth;horf, g&oacute;&eth;a a&eth;l&ouml;gunarh&aelig;fni og getu til a&eth; takast &aacute; vi&eth; &aacute;skoranir.&nbsp;Vinna &aacute; dag- og kv&ouml;ldv&ouml;ktum er nau&eth;synleg.
&THORN;essi sta&eth;a b&yacute;&eth;ur upp &aacute; hagn&yacute;ta reynslu &iacute; al&thorn;j&oacute;&eth;legu umhverfi &aacute;samt fj&ouml;lbreyttum t&aelig;kif&aelig;rum til starfs&thorn;r&oacute;unar!

Helstu verkefni og &aacute;byrg&eth;:
<ul>
<li>
Flutningur framlei&eth;sluefna fr&aacute; v&ouml;ruh&uacute;si yfir &iacute; Class D sv&aelig;&eth;i.
</li>
<li>
Fylla &aacute; og vi&eth;halda Kanban efnaherbergjum &aacute; DSM1 og DSM2 sv&aelig;&eth;um.
</li>
<li>
Tryggja a&eth; framlei&eth;slu&aacute;&aelig;tlun s&eacute; uppf&aelig;r&eth;.
</li>
<li>
Sty&eth;ja vi&eth; heildarframlei&eth;slu og tryggja a&eth; &aacute;&aelig;tlanager&eth; s&eacute; r&eacute;tt framkv&aelig;md.
</li>
</ul>

H&aelig;fniskr&ouml;fur:
<ul>
<li>
Grunn&thorn;ekking &aacute; vi&eth;eigandi ferlum og t&aelig;kni.
</li>
<li>
Fram&uacute;rskarandi samskiptah&aelig;fileikar.
</li>
<li>
Geta til a&eth; vinna &iacute; teymi.
</li>
<li>
Stundv&iacute;si og &aacute;rei&eth;anleiki.
</li>
<li>
Sveigjanleiki og g&oacute;&eth; a&eth;l&ouml;gunarh&aelig;fni.
</li>
</ul>

[English]

Join our production team at Alvotech in Reykjav&iacute;k!
We are looking for individuals with a positive attitude, strong adaptability, and the ability to tackle challenges.&nbsp;Working day and evening shifts is required.
This position offers hands-on experience in an international environment along with diverse opportunities for professional development!

Key Responsibilities:
<ul>
<li>
Material transfer of process materials from Warehouse to Class D area.
</li>
<li>
To stock up and maintain Kanban material rooms in DSM1 and DSM2 areas.
</li>
<li>
Ensure to update planning related activities.
</li>
<li>
To support overall manufacturing &amp; ensure planning is performed properly.
</li>
</ul>

Qualifications:
<ul>
<li>
Basic technical or administrative knowledge or relevant process knowledge.
</li>
<li>
Adhere to the company etiquette in all matters of behavior and manners.
</li>
<li>
Excellent communication skills.
</li>
<li>
Strong work ethic and proven ability to collaborate effectively in team
</li>
<li>
Punctual and reliable.
</li>
<li>
Flexible/adaptable.
</li>
</ul>

What we offer:
<ul>
<li>
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.
</li>
<li>
The chance to be a part of a global and fast-growing company.
</li>
<li>
An international work culture that encourages diversity, collaboration and inclusion.
</li>
<li>
Positive, flexible, and innovative work environment.
</li>
<li>
Support for personal growth and internal career development.
</li>
<li>
Company social events and milestone celebrations.
</li>
<li>
Excellent in-house canteen and coffee house.
</li>
<li>
Exercise and wellbeing support for full-time employees.
</li>
<li>
On-site shower facility.
</li>
<li>
Transportation grant towards eco-friendly modes of travel for full-time employees.
</li>
<li>
Internet at home for full-time employees.
</li>
</ul>

About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
&nbsp;
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
&nbsp;
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com


Gakktu til liðs við framleiðsluteymið hjá Alvotech í Reykjavík! Við leitum að einstaklingum með jákvætt viðhorf, góða aðlögunarhæfni og getu til að takast á við áskoranir.
Vinna á dag- og kvöldvöktum er nauðsynleg.

Þessi staða býður upp á hagnýta reynslu í alþjóðlegu umhverfi ásamt fjölbreyttum tækifærum til starfsþróunar!



Helstu verkefni og ábyrgð:


 - 

Flutningur framleiðsluefna frá vöruhúsi yfir í Class D svæði.


 - 

Fylla á og viðhalda Kanban efnaherbergjum á DSM1 og DSM2 svæðum.


 - 

Tryggja að framleiðsluáætlun sé uppfærð.


 - 

Styðja við heildarframleiðslu og tryggja að áætlanagerð sé rétt framkvæmd.





Hæfniskröfur:


 - 

Grunnþekking á viðeigandi ferlum og tækni.


 - 

Framúrskarandi samskiptahæfileikar.


 - 

Geta til að vinna í teymi.


 - 

Stundvísi og áreiðanleiki.


 - 

Sveigjanleiki og góð aðlögunarhæfni.





[English]



Join our production team at Alvotech in Reykjavík!

We are looking for individuals with a positive attitude, strong adaptability, and the ability to tackle challenges.
Working day and evening shifts is required.

This position offers hands-on experience in an international environment along with diverse opportunities for professional development!



Key Responsibilities:


 - 

Material transfer of process materials from Warehouse to Class D area.


 - 

To stock up and maintain Kanban material rooms in DSM1 and DSM2 areas.


 - 

Ensure to update planning related activities.


 - 

To support overall manufacturing &amp; ensure planning is performed properly.





Qualifications:


 - 

Basic technical or administrative knowledge or relevant process knowledge.


 - 

Adhere to the company etiquette in all matters of behavior and manners.


 - 

Excellent communication skills.


 - 

Strong work ethic and proven ability to collaborate effectively in team


 - 

Punctual and reliable.


 - 

Flexible/adaptable.





What we offer:


 - 

An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.


 - 

The chance to be a part of a global and fast-growing company.


 - 

An international work culture that encourages diversity, collaboration and inclusion.


 - 

Positive, flexible, and innovative work environment.


 - 

Support for personal growth and internal career development.


 - 

Company social events and milestone celebrations.


 - 

Excellent in-house canteen and coffee house.


 - 

Exercise and wellbeing support for full-time employees.


 - 

On-site shower facility.


 - 

Transportation grant towards eco-friendly modes of travel for full-time employees.


 - 

Internet at home for full-time employees.





About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.




We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.




Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.



If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.



If you have any technical issues, please contact: hr@alvotech.com

Framleiðslutæknir / Manufacturing Technologist

Overview of Role
We are looking for capable and motivated formulation scientist&nbsp;to join the Drug Product Development team at Alvotech, Reykjavik. In this position, you will be a part of a team working on the development of liquid/lyophilized biologics (biosimilar) drug products. This role is an excellent opportunity for both recent graduates and experienced scientists who are eager to build or expand their expertise in biopharmaceutical development.
Scope and responsibility
<ul>
<li>
Perform activities related to the development of liquid/lyophilized formulations (early- and late-stage development), selection of excipient raw materials and formulation characterization to ensure that a sufficiently robust formulation has been developed.
</li>
<li>
Design, perform, and report formulation screening experiments, stability studies, biophysical characterization and other studies leading to the development of stable formulations according to Quality by Design (QbD) principles and internal policies.
</li>
<li>
Work closely with the Process Development and Material Science teams within Drug Product Development to ensure compatibility of the formulations with the manufacturing process (including lyophilization) and container closure systems.
</li>
</ul>
In this role you will gain experience in formulation development of biologics, including:
<ul>
<li>
Understanding and optimizing &nbsp;protein stability and intermolecular interactions
</li>
<li>
Evaluating&nbsp;critical&nbsp;quality attributes (CQAs) such as aggregation, degradation, and physicochemical stability
</li>
<li>
Studying how proteins behave under&nbsp;stress conditions (e.g. temperature, agitation, pH)
</li>
<li>
Designing and analyzing experiments using&nbsp;Design of Experiments (DoE) and statistical tools
</li>
<li>
Interpreting&nbsp;degradation&nbsp;pathways and stability profiles to design robust formulations.
</li>
</ul>
Job requirements
We are looking for flexible, open-minded and motivated scientists that are excited about biopharmaceutical development, can challenge their work by innovative and creative solutions, and share our values of team spirit and team efforts. The specific requirements for the role are detailed below.
<ul>
<li>
MSc (or PhD) in biochemistry, biophysics, biotechnology, chemistry, pharmaceutical science or other related disciplines.
</li>
<li>
Proactive team player with strong communication, organization and presentation skills.
</li>
<li>
Prior experience in biopharmaceutical development, formulation, or a related field is considered an advantage, but not required.
</li>
<li>
Strong foundation in protein chemistry, stability and molecular interactions is advantageous.
</li>
</ul>
What we offer:
<ul>
<li>
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.
</li>
<li>
The chance to be a part of a global and fast-growing company.
</li>
<li>
An international work culture that encourages diversity, collaboration, and inclusion.
</li>
<li>
Positive, flexible, and innovative work environment.
</li>
<li>
Support for personal growth and internal career development.
</li>
<li>
Company social events and milestone celebrations.
</li>
<li>
Excellent in-house canteen and coffee house.
</li>
<li>
Exercise and well-being support for full-time employees.
</li>
<li>
On-site shower facility.
</li>
<li>
Transportation grant towards eco-friendly modes of travel for full-time employees.
</li>
</ul>
Internet at home for full-time employees. About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.
If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.
If you have any technical issues, please contact: hr@alvotech.com


Overview of Role

We are looking for capable and motivated formulation scientist
to join the Drug Product Development team at Alvotech, Reykjavik. In this position, you will be a part of a team working on the development of liquid/lyophilized biologics (biosimilar) drug products. This role is an excellent opportunity for both recent graduates and experienced scientists who are eager to build or expand their expertise in biopharmaceutical development.

Scope and responsibility


 - 

Perform activities related to the development of liquid/lyophilized formulations (early- and late-stage development), selection of excipient raw materials and formulation characterization to ensure that a sufficiently robust formulation has been developed.


 - 

Design, perform, and report formulation screening experiments, stability studies, biophysical characterization and other studies leading to the development of stable formulations according to Quality by Design (QbD) principles and internal policies.


 - 

Work closely with the Process Development and Material Science teams within Drug Product Development to ensure compatibility of the formulations with the manufacturing process (including lyophilization) and container closure systems.



In this role you will gain experience in formulation development of biologics, including:


 - 

Understanding and optimizing 
protein stability and intermolecular interactions


 - 

Evaluating
critical
quality attributes (CQAs) such as aggregation, degradation, and physicochemical stability


 - 

Studying how proteins behave under
stress conditions (e.g. temperature, agitation, pH)


 - 

Designing and analyzing experiments using
Design of Experiments (DoE) and statistical tools


 - 

Interpreting
degradation
pathways and stability profiles to design robust formulations.



Job requirements

We are looking for flexible, open-minded and motivated scientists that are excited about biopharmaceutical development, can challenge their work by innovative and creative solutions, and share our values of team spirit and team efforts. The specific requirements for the role are detailed below.


 - 

MSc (or PhD) in biochemistry, biophysics, biotechnology, chemistry, pharmaceutical science or other related disciplines.


 - 

Proactive team player with strong communication, organization and presentation skills.


 - 

Prior experience in biopharmaceutical development, formulation, or a related field is considered an advantage, but not required.


 - 

Strong foundation in protein chemistry, stability and molecular interactions is advantageous.



What we offer:


 - 

An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.


 - 

The chance to be a part of a global and fast-growing company.


 - 

An international work culture that encourages diversity, collaboration, and inclusion.


 - 

Positive, flexible, and innovative work environment.


 - 

Support for personal growth and internal career development.


 - 

Company social events and milestone celebrations.


 - 

Excellent in-house canteen and coffee house.


 - 

Exercise and well-being support for full-time employees.


 - 

On-site shower facility.


 - 

Transportation grant towards eco-friendly modes of travel for full-time employees.



Internet at home for full-time employees.

About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.

We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.

Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com

Scientist, Drug Product Development

Nowe oferty

Główny specjalista, DSP MSAT

Starszy Specjalista ds. Operacji Produkcyjnych

Technolog produkcji

Naukowiec, Rozwój Produktów Leczniczych

Overview of role:&nbsp; Are you a subject matter expert in upstream processing with a passion for innovation and technical excellence in biologics manufacturing? Alvotech is seeking a USP MSAT Specialist &ndash; Late Stage to lead upstream process support, scale-up, and lifecycle management for commercial biosimilar products. Key Responsibilities:
<ul>
<li>Act as the&nbsp;Subject Matter Expert (SME)&nbsp;for upstream manufacturing processes, providing technical leadership and guidance.</li>
<li>Lead&nbsp;process scale-up and technology transfer&nbsp;from development to GMP manufacturing (clinical and commercial), including defining scale-up strategies and ensuring successful implementation across internal and external sites.</li>
<li>Provide&nbsp;independent technical support to manufacturing, including process monitoring, troubleshooting, and advanced data analysis to anticipate and resolve issues proactively.</li>
<li>Investigate&nbsp;manufacturing deviations, perform root cause analysis, and implement effective&nbsp;CAPAs.</li>
<li>Author, review, and approve&nbsp;process and regulatory documentation, including PDDs, protocols, reports, change controls, and regulatory submissions.</li>
<li>Support the&nbsp;introduction, qualification, and ongoing optimization of upstream processes&nbsp;in cGMP manufacturing, managing associated technical risks.</li>
<li>Lead and contribute to&nbsp;process optimization and continuous improvement initiatives, enhancing yield, robustness, and cost-efficiency.</li>
<li>Support&nbsp;lifecycle management of commercial products, including Continued Process Verification (CPV), process changes, and ongoing process monitoring.</li>
<li>Assess, qualify, and introduce&nbsp;new materials, technologies, and innovations&nbsp;to improve manufacturing performance and efficiency.</li>
<li>Collaborate with and represent MSAT in&nbsp;cross-functional and cross-site teams, driving technical solutions, effective communication, and project delivery.</li>
<li>Ensure&nbsp;compliance with cGMP, regulatory, and EHS requirements&nbsp;in all activities.</li>
<li>Proactively&nbsp;identify, evaluate, and resolve technical challenges, leveraging expertise and continuous learning to improve processes.</li>
<li>Contribute to&nbsp;project execution and timelines, influencing technical decisions and ensuring alignment with business objectives. &nbsp;</li>
</ul>
Qualifications:
<ul>
<li>Master&rsquo;s degree in Life Sciences (Biotechnology or related field).</li>
<li>5&ndash;10 years of experience in the biopharmaceutical industry, with a focus on upstream processing, process development, manufacturing, or MSAT.</li>
<li>Strong knowledge of monoclonal antibody manufacturing and industrial biotechnology.</li>
<li>Experience in GMP environments and regulatory compliance.</li>
<li>Proven ability to work independently, manage complex technical challenges, and lead cross-functional teams. &nbsp;</li>
</ul>
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
</ul>
Internet at home for full-time employees. About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.
If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.
If you have any technical issues, please contact: hr@alvotech.com


Overview of role:


Are you a subject matter expert in upstream processing with a passion for innovation and technical excellence in biologics manufacturing? Alvotech is seeking a USP MSAT Specialist – Late Stage to lead upstream process support, scale-up, and lifecycle management for commercial biosimilar products.

Key Responsibilities:


 - Act as the
Subject Matter Expert (SME)
for upstream manufacturing processes, providing technical leadership and guidance.

 - Lead
process scale-up and technology transfer
from development to GMP manufacturing (clinical and commercial), including defining scale-up strategies and ensuring successful implementation across internal and external sites.

 - Provide
independent technical support to manufacturing, including process monitoring, troubleshooting, and advanced data analysis to anticipate and resolve issues proactively.

 - Investigate
manufacturing deviations, perform root cause analysis, and implement effective
CAPAs.

 - Author, review, and approve
process and regulatory documentation, including PDDs, protocols, reports, change controls, and regulatory submissions.

 - Support the
introduction, qualification, and ongoing optimization of upstream processes
in cGMP manufacturing, managing associated technical risks.

 - Lead and contribute to
process optimization and continuous improvement initiatives, enhancing yield, robustness, and cost-efficiency.

 - Support
lifecycle management of commercial products, including Continued Process Verification (CPV), process changes, and ongoing process monitoring.

 - Assess, qualify, and introduce
new materials, technologies, and innovations
to improve manufacturing performance and efficiency.

 - Collaborate with and represent MSAT in
cross-functional and cross-site teams, driving technical solutions, effective communication, and project delivery.

 - Ensure
compliance with cGMP, regulatory, and EHS requirements
in all activities.

 - Proactively
identify, evaluate, and resolve technical challenges, leveraging expertise and continuous learning to improve processes.

 - Contribute to
project execution and timelines, influencing technical decisions and ensuring alignment with business objectives.




Qualifications:


 - Master’s degree in Life Sciences (Biotechnology or related field).

 - 5–10 years of experience in the biopharmaceutical industry, with a focus on upstream processing, process development, manufacturing, or MSAT.

 - Strong knowledge of monoclonal antibody manufacturing and industrial biotechnology.

 - Experience in GMP environments and regulatory compliance.

 - Proven ability to work independently, manage complex technical challenges, and lead cross-functional teams.




What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.


Internet at home for full-time employees.

About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.

We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.

Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com

Starszy Specjalista, USP MSAT

&Iacute;slenska:
Vilt &thorn;&uacute; ver&eth;a hluti af Drug Substance Operations teyminu hj&aacute; Alvotech &iacute; Reykjav&iacute;k og starfa &iacute; &ouml;flugu og faglegu umhverfi &thorn;ar sem n&aacute;kv&aelig;mni, g&aelig;&eth;i og samvinna skipta m&aacute;li?
Vi&eth; leitum a&eth; j&aacute;kv&aelig;&eth;um og lausnami&eth;u&eth;um einstaklingum sem eru tilb&uacute;nir a&eth; takast &aacute; spennandi &aacute;skoranir. Vi&eth; bj&oacute;&eth;um upp &aacute; vanda&eth;a &thorn;j&aacute;lfun, g&oacute;&eth;a handlei&eth;slu og t&aelig;kif&aelig;ri til a&eth; vaxa &iacute; starfi. &nbsp;
English Overview of role:&nbsp;
Join the Drug Substance Operations Team at Alvotech in Reykjavik and be a part of a dynamic, highly regulated environment where attention to detail and thoroughness are key. We're seeking individuals who are proactive, embrace challenges and have a positive mindset. The role requires extensive training, and Alvotech prioritizes teaching, mentoring, and guiding its technicians.&nbsp;Working in day/evening/night shifts is required. Key Responsibilities: 
<ul>
<li>Perform all activities in full compliance with current Good Manufacturing Practices (cGMP) and Environment, Health &amp; Safety (EHS) standards, ensuring work is executed in a safe and compliant manner. Demonstrate willingness to take on additional tasks under appropriate supervision.</li>
<li>Execute cGMP manufacturing activities within Grade CNC, D, and C classified areas, adhering strictly to aseptic and containment requirements.</li>
<li>Aseptically culture mammalian cells in shake flasks through the completion of the production process using single-use bioreactor systems, in accordance with approved protocols.</li>
<li>Prepare media and buffers to defined specifications following approved standard operating procedures and batch documentation.</li>
<li>Proactively maintain the USP manufacturing suite and associated equipment in a perpetual state of inspection readiness, ensuring compliance with regulatory and internal quality standards.</li>
<li>Actively participate as a reviewer of cGMP documentation within the individual&rsquo;s area of expertise.</li>
<li>Support the execution of technical studies and validation activities, including process and equipment qualification, under approved protocols.</li>
<li>Support successful regulatory inspections, including Pre-Approval Inspections (PAIs), and routine audits.</li>
<li>Demonstrate a strong commitment to operational excellence, continuous improvement, and right-first-time execution within the assigned functional area.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor&rsquo;s or technical degree in biotechnology, chemistry, biochemistry, biochemical engineering, or science related fields (desirable)</li>
<li>No prior experience required, but laboratory experience is a plus</li>
<li>Proficiency in Microsoft Office programs (Word, Excel)</li>
<li>Excellent command of English language</li>
<li>Ability to multitask and work both independently and as part of a team</li>
</ul>
What we offer: 
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.
If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.
If you have any technical issues, please contact: hr@alvotech.com


Íslenska:

Vilt þú verða hluti af Drug Substance Operations teyminu hjá Alvotech í Reykjavík og starfa í öflugu og faglegu umhverfi þar sem nákvæmni, gæði og samvinna skipta máli?

Við leitum að jákvæðum og lausnamiðuðum einstaklingum sem eru tilbúnir að takast á spennandi áskoranir. Við bjóðum upp á vandaða þjálfun, góða handleiðslu og tækifæri til að vaxa í starfi.



English

Overview of role:


Join the Drug Substance Operations Team at Alvotech in Reykjavik and be a part of a dynamic, highly regulated environment where attention to detail and thoroughness are key. We're seeking individuals who are proactive, embrace challenges and have a positive mindset. The role requires extensive training, and Alvotech prioritizes teaching, mentoring, and guiding its technicians.
Working in day/evening/night shifts is required.

Key Responsibilities: 


 - Perform all activities in full compliance with current Good Manufacturing Practices (cGMP) and Environment, Health &amp; Safety (EHS) standards, ensuring work is executed in a safe and compliant manner. Demonstrate willingness to take on additional tasks under appropriate supervision.

 - Execute cGMP manufacturing activities within Grade CNC, D, and C classified areas, adhering strictly to aseptic and containment requirements.

 - Aseptically culture mammalian cells in shake flasks through the completion of the production process using single-use bioreactor systems, in accordance with approved protocols.

 - Prepare media and buffers to defined specifications following approved standard operating procedures and batch documentation.

 - Proactively maintain the USP manufacturing suite and associated equipment in a perpetual state of inspection readiness, ensuring compliance with regulatory and internal quality standards.

 - Actively participate as a reviewer of cGMP documentation within the individual’s area of expertise.

 - Support the execution of technical studies and validation activities, including process and equipment qualification, under approved protocols.

 - Support successful regulatory inspections, including Pre-Approval Inspections (PAIs), and routine audits.

 - Demonstrate a strong commitment to operational excellence, continuous improvement, and right-first-time execution within the assigned functional area.


Qualifications:


 - Bachelor’s or technical degree in biotechnology, chemistry, biochemistry, biochemical engineering, or science related fields (desirable)

 - No prior experience required, but laboratory experience is a plus

 - Proficiency in Microsoft Office programs (Word, Excel)

 - Excellent command of English language

 - Ability to multitask and work both independently and as part of a team


What we offer: 


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.


About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.

We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.

Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com

Ekscytująca szansa dla absolwentów kierunków ścisłych – produkcja biotechnologiczna

Alvotech is looking for&nbsp;a&nbsp;Director of Group Consolidation &amp; Financial Reporting&nbsp;to lead and strengthen our global financial reporting function. This is a key role within the finance team, responsible for overseeing the group consolidation process, ensuring high-quality IFRS reporting, and supporting complex technical accounting matters across our international operations. The role offers the opportunity to work in a dynamic, fast-growing global environment and to partner closely with senior stakeholders across the organization.

Key Responsibilities
<ul>
<li>
Lead and support monthly, quarterly, and annual group consolidation processes, ensuring accuracy, completeness, and timeliness of financial information
</li>
<li>
Prepare and review manual consolidation adjustments (e.g. intercompany eliminations, FX, equity accounting) and maintain consolidation rules and reporting structures
</li>
<li>
Prepare and review consolidated IFRS financial statements and statutory accounts for key legal entities, including disclosures and supporting documentation
</li>
<li>
Act as key contact for external auditors and support audit processes end-to-end
</li>
<li>
Analyze and support complex IFRS accounting matters and ensure consistent application of accounting policies across the group
</li>
<li>
Monitor new accounting standards and assess their impact on the business
</li>
<li>
Collaborate with group and local finance teams and cross-functional stakeholders (Tax, FP&amp;A, Treasury, Legal, Systems)
</li>
<li>
Provide technical accounting insights to senior management
</li>
<li>
Drive continuous improvement of consolidation, reporting processes, systems, and internal controls
</li>
</ul>

Qualifications
<ul>
<li>
Master&rsquo;s degree in Accounting, Finance, or a related field; professional certification (e.g. Icelandic CPA or equivalent) is a plus
</li>
<li>
5&ndash;10 years of experience in group consolidation, financial reporting, or technical accounting
</li>
<li>
Strong IFRS knowledge and hands-on experience with consolidated reporting and group close processes
</li>
<li>
Experience in a listed environment and/or Big 4 background is highly desirable
</li>
<li>
Advanced Excel skills and experience with&nbsp;consolidation/reporting&nbsp;systems (e.g. SAP)
</li>
<li>
Strong analytical skills, attention to detail, and ability to meet tight deadlines
</li>
<li>
Structured, hands-on, and comfortable in a fast-paced international environment
</li>
<li>
Strong communication skills, with ability to engage senior stakeholders
</li>
<li>
High integrity and sound professional judgment
</li>
</ul>

What we offer
<ul>
<li>
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.
</li>
<li>
The chance to be a part of a global and fast-growing company.
</li>
<li>
An international work culture that encourages diversity, collaboration and inclusion.
</li>
<li>
Positive, flexible, and innovative work environment.
</li>
<li>
Support for personal growth and internal career development.
</li>
<li>
Company social events and milestone celebrations.
</li>
<li>
Excellent in-house canteen and coffee house.
</li>
<li>
Exercise and wellbeing support for full-time employees.
</li>
<li>
On-site shower facility.
</li>
<li>
Transportation grant towards eco-friendly modes of travel for full-time employees.
</li>
<li>
Internet at home for full-time employees.
</li>
</ul>


Alvotech is looking for
a
Director of Group Consolidation &amp; Financial Reporting
to lead and strengthen our global financial reporting function. This is a key role within the finance team, responsible for overseeing the group consolidation process, ensuring high-quality IFRS reporting, and supporting complex technical accounting matters across our international operations. The role offers the opportunity to work in a dynamic, fast-growing global environment and to partner closely with senior stakeholders across the organization.



Key Responsibilities


 - 

Lead and support monthly, quarterly, and annual group consolidation processes, ensuring accuracy, completeness, and timeliness of financial information


 - 

Prepare and review manual consolidation adjustments (e.g. intercompany eliminations, FX, equity accounting) and maintain consolidation rules and reporting structures


 - 

Prepare and review consolidated IFRS financial statements and statutory accounts for key legal entities, including disclosures and supporting documentation


 - 

Act as key contact for external auditors and support audit processes end-to-end


 - 

Analyze and support complex IFRS accounting matters and ensure consistent application of accounting policies across the group


 - 

Monitor new accounting standards and assess their impact on the business


 - 

Collaborate with group and local finance teams and cross-functional stakeholders (Tax, FP&amp;A, Treasury, Legal, Systems)


 - 

Provide technical accounting insights to senior management


 - 

Drive continuous improvement of consolidation, reporting processes, systems, and internal controls





Qualifications


 - 

Master’s degree in Accounting, Finance, or a related field; professional certification (e.g. Icelandic CPA or equivalent) is a plus


 - 

5–10 years of experience in group consolidation, financial reporting, or technical accounting


 - 

Strong IFRS knowledge and hands-on experience with consolidated reporting and group close processes


 - 

Experience in a listed environment and/or Big 4 background is highly desirable


 - 

Advanced Excel skills and experience with
consolidation/reporting
systems (e.g. SAP)


 - 

Strong analytical skills, attention to detail, and ability to meet tight deadlines


 - 

Structured, hands-on, and comfortable in a fast-paced international environment


 - 

Strong communication skills, with ability to engage senior stakeholders


 - 

High integrity and sound professional judgment





What we offer


 - 

An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.


 - 

The chance to be a part of a global and fast-growing company.


 - 

An international work culture that encourages diversity, collaboration and inclusion.


 - 

Positive, flexible, and innovative work environment.


 - 

Support for personal growth and internal career development.


 - 

Company social events and milestone celebrations.


 - 

Excellent in-house canteen and coffee house.


 - 

Exercise and wellbeing support for full-time employees.


 - 

On-site shower facility.


 - 

Transportation grant towards eco-friendly modes of travel for full-time employees.


 - 

Internet at home for full-time employees.

