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

Strona internetowa

Facebook

Instagram

LinkedIn

Ruch

Transport i komunikacja

Posiłek

Rozrywka

Środowisko pracy

&Iacute;slenska Gakktu til li&eth;s vi&eth; framlei&eth;sluteymi hj&aacute; Alvotech &iacute; Reykjav&iacute;k!&nbsp;Alvotech starfar &iacute; reglubundnu umhverfi &thorn;ar sem n&aacute;kv&aelig;mni og samviskusemi skipta sk&ouml;pum. Vi&eth; leitum a&eth; einstaklingum me&eth; j&aacute;kv&aelig;tt hugarfar, g&oacute;&eth;a a&eth;l&ouml;gunarh&aelig;fni og h&aelig;fni til a&eth; takast &aacute; vi&eth; &aacute;skoranir.&nbsp;Vaktavinna er nau&eth;synleg og felur &iacute; s&eacute;r dag-, kv&ouml;ld- og n&aelig;turvaktir.
H&aelig;fniskr&ouml;fur:
<ul>
<li>
A&eth; l&aacute;gmarki 3 &aacute;ra reynsla &iacute; lyfjai&eth;na&eth;i.
</li>
<li>
G&oacute;&eth; reynsla af vinnu &iacute; A og B vottu&eth;u umhverfi.
</li>
<li>
Menntun: BS e&eth;a dipl&oacute;ma &iacute; t&aelig;knigreinum, (t.d. l&iacute;ft&aelig;kni, verkfr&aelig;&eth;i, l&iacute;fefnafr&aelig;&eth;i) er kostur en ekki skilyr&eth;i.
</li>
<li>
&THORN;ekking &aacute; g&oacute;&eth;um framlei&eth;slu h&aacute;ttum (GMP) og h&aelig;fni til a&eth; fylgja verklagsreglum vi&eth; skr&aacute;ningar.
</li>
<li>
H&aelig;fni til &thorn;ess a&eth; vinna vel &iacute; teymi.
</li>
<li>
G&oacute;&eth; enskukunn&aacute;tta.
</li>
</ul>
[English]
&nbsp;
Overview of Role&nbsp;
Join the Drug Product Manufacturing Team at Alvotech in Reykjavik! Alvotech operates in a highly regulated environment that requires attention to detail and thoroughness. We're seeking someone with strong leadership skills, a positive attitude, and the ability to adapt to challenges.&nbsp;Working day, evening, and night shifts is required.
&nbsp;
Scope and responsibility:
<ul>
<li>
Work in accordance with cGMP standards across various cleanroom zones (Grade A, B, C, and CNC).
</li>
<li>
Be part of a collaborative team working to meet the drug product (DP) manufacturing schedule.
</li>
<li>
Serve as a Subject Matter Expert for PAIs, audits and regulatory agency interactions.
</li>
<li>
Author, review and approve written procedures, SOPs, deviations, CAPAs and change controls.
</li>
<li>
Ensure DP manufacturing area and equipment are in inspection-ready state through interaction with Engineering, Facilities, and EHS.
</li>
<li>
Continuously identify opportunities for process improvement and waste elimination to maintain a lean, flexible and agile manufacturing facility. &nbsp;
</li>
</ul>
Job requirements:
<ul>
<li>
3+ years in (bio)pharmaceuticals is required.
</li>
<li>
Good experience working in grade A and B environment.
</li>
<li>
Education: BSc or Diploma in a Technical Discipline (e.g., biotechnology, engineering, biochemistry or related field) is advantage but not a requirement.
</li>
<li>
Knowledge of Good Manufacturing Practices (GMP), documentation rules, and an ability to follow the documentation for the execution of batch records, SOPs and work instructions is required.
</li>
<li>
Ability to work well in a team.
</li>
<li>
Proficient English skills, Icelandic language not required.
</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>

Why Alvotech : &nbsp;At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We&rsquo;re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment. True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let&rsquo;s create a healthier world together, through affordable biologic medicines.

Alvotech hf


Íslenska

Gakktu til liðs við framleiðsluteymi hjá Alvotech í Reykjavík!
Alvotech starfar í reglubundnu umhverfi þar sem nákvæmni og samviskusemi skipta sköpum. Við leitum að einstaklingum með jákvætt hugarfar, góða aðlögunarhæfni og hæfni til að takast á við áskoranir.
Vaktavinna er nauðsynleg og felur í sér dag-, kvöld- og næturvaktir.

Hæfniskröfur:


 - 

Að lágmarki 3 ára reynsla í lyfjaiðnaði.


 - 

Góð reynsla af vinnu í A og B vottuðu umhverfi.


 - 

Menntun: BS eða diplóma í tæknigreinum, (t.d. líftækni, verkfræði, lífefnafræði) er kostur en ekki skilyrði.


 - 

Þekking á góðum framleiðslu háttum (GMP) og hæfni til að fylgja verklagsreglum við skráningar.


 - 

Hæfni til þess að vinna vel í teymi.


 - 

Góð enskukunnátta.



[English]




Overview of Role


Join the Drug Product Manufacturing Team at Alvotech in Reykjavik! Alvotech operates in a highly regulated environment that requires attention to detail and thoroughness. We're seeking someone with strong leadership skills, a positive attitude, and the ability to adapt to challenges.
Working day, evening, and night shifts is required.




Scope and responsibility:


 - 

Work in accordance with cGMP standards across various cleanroom zones (Grade A, B, C, and CNC).


 - 

Be part of a collaborative team working to meet the drug product (DP) manufacturing schedule.


 - 

Serve as a Subject Matter Expert for PAIs, audits and regulatory agency interactions.


 - 

Author, review and approve written procedures, SOPs, deviations, CAPAs and change controls.


 - 

Ensure DP manufacturing area and equipment are in inspection-ready state through interaction with Engineering, Facilities, and EHS.


 - 

Continuously identify opportunities for process improvement and waste elimination to maintain a lean, flexible and agile manufacturing facility.





Job requirements:


 - 

3+ years in (bio)pharmaceuticals is required.


 - 

Good experience working in grade A and B environment.


 - 

Education: BSc or Diploma in a Technical Discipline (e.g., biotechnology, engineering, biochemistry or related field) is advantage but not a requirement.


 - 

Knowledge of Good Manufacturing Practices (GMP), documentation rules, and an ability to follow the documentation for the execution of batch records, SOPs and work instructions is required.


 - 

Ability to work well in a team.


 - 

Proficient English skills, Icelandic language not required.



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.





Why Alvotech :


At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We’re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment.

True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let’s create a healthier world together, through affordable biologic medicines.

Active

Senior Aseptic Manufacturing Technician/ Yfirframleiðslutæknir í Smitgátarframleiðslu

Alvotech is a fully integrated specialty biopharmaceutical company dedicated exclusively to the development and manufacturing of high-quality biosimilar medicines. Our mission is to improve lives worldwide by increasing access to affordable biologic treatments.
The Environment, Health &amp; Safety (EHS) department plays a vital role in creating and maintaining a safe, healthy, and compliant workplace across Alvotech&rsquo;s operations. Partnering closely with employees, managers, contractors, and external stakeholders, the team drives a proactive safety culture, ensures regulatory compliance, and supports continuous improvement initiatives throughout the organization.
Overview of the Role
Alvotech is seeking an EHS Specialist to support our manufacturing operations in Reykjavik, Iceland. This is an exciting opportunity for biotechnology, scientific, or health and safety professionals who are passionate about workplace safety and eager to contribute to a growing global biopharmaceutical company.
In this role, you will support the implementation, maintenance, and continuous enhancement of EHS programs within a dynamic manufacturing environment. Working alongside a dedicated EHS team, you will provide expert guidance on safety standards and best practices, contribute to compliance initiatives, and help strengthen a culture where health, safety, and operational excellence are at the forefront of everything we do.
Key Responsibilities
<ul>
<li>Support the management of EHS programs, training activities, and the facilitation of EHS risk assessments.</li>
<li>Provide guidance to Alvotech employees, contractors, vendors, and visitors on EHS standards, expectations, and company guidelines within manufacturing areas.</li>
<li>Advise teams on EHS requirements and best practices in manufacturing environments.</li>
<li>Lead and participate in internal audits, inspections, and compliance activities.</li>
<li>Contribute to the implementation of industry best practices and continuous improvement initiatives.</li>
</ul>
Minimum Education and Experience Required for the Role
<ul>
<li>University degree in Biotechnology, Chemistry, Engineering, or a related scientific discipline.</li>
<li>Degree-level education, preferably in a scientific, technical, or engineering field.</li>
<li>At least 1 year of experience in a Health &amp; Safety role within a regulated industry.</li>
<li>Understanding of biotechnology manufacturing processes, including relevant methods, techniques, and equipment.</li>
<li>Strong written, verbal, and interpersonal communication skills.</li>
<li>Proactive mindset with sound judgment and decision-making abilities.</li>
<li>Demonstrated ability to work independently, solve problems effectively, and manage multiple priorities in a fast-paced environment.</li>
<li>Candidates without direct EHS experience are encouraged to apply if they possess a relevant educational background, laboratory safety experience, and a strong interest in building a career within EHS.</li>
</ul>
What We Offer
<ul>
<li>The opportunity to work alongside talented colleagues on meaningful projects that improve patients&rsquo; lives.</li>
<li>A chance to be part of a global, innovative, and rapidly growing biopharmaceutical company.</li>
<li>An international and inclusive culture that values diversity, collaboration, and respect.</li>
<li>A positive, flexible, and forward-thinking work environment.</li>
<li>Ongoing opportunities for personal development and internal career growth.</li>
<li>Company social events, celebrations, and team-building activities.</li>
<li>Excellent on-site canteen and coffee house facilities.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facilities.</li>
<li>Transportation grant supporting eco-friendly commuting options for full-time employees.</li>
<li>Home internet support for full-time employees.</li>
</ul>
Why Alvotech?
At Alvotech, we are passionate about improving lives by increasing access to affordable biologic medicines. As a purpose-driven organization, we foster an inclusive environment where curiosity, innovation, and simplicity are valued. We empower our employees to take ownership of their careers, embrace meaningful challenges, and thrive in a fast-moving and collaborative setting.
True to our Icelandic roots, we are committed to integrity, fairness, gender equality, and respect for diverse perspectives. We believe that bringing together talented individuals from different backgrounds enables us to deliver exceptional results for our partners and patients around the world.
Join us in shaping a healthier future and creating greater access to life-changing biologic medicines worldwide.
&nbsp;


Alvotech is a fully integrated specialty biopharmaceutical company dedicated exclusively to the development and manufacturing of high-quality biosimilar medicines. Our mission is to improve lives worldwide by increasing access to affordable biologic treatments.

The Environment, Health &amp; Safety (EHS) department plays a vital role in creating and maintaining a safe, healthy, and compliant workplace across Alvotech’s operations. Partnering closely with employees, managers, contractors, and external stakeholders, the team drives a proactive safety culture, ensures regulatory compliance, and supports continuous improvement initiatives throughout the organization.

Overview of the Role

Alvotech is seeking an EHS Specialist to support our manufacturing operations in Reykjavik, Iceland. This is an exciting opportunity for biotechnology, scientific, or health and safety professionals who are passionate about workplace safety and eager to contribute to a growing global biopharmaceutical company.

In this role, you will support the implementation, maintenance, and continuous enhancement of EHS programs within a dynamic manufacturing environment. Working alongside a dedicated EHS team, you will provide expert guidance on safety standards and best practices, contribute to compliance initiatives, and help strengthen a culture where health, safety, and operational excellence are at the forefront of everything we do.

Key Responsibilities


 - Support the management of EHS programs, training activities, and the facilitation of EHS risk assessments.

 - Provide guidance to Alvotech employees, contractors, vendors, and visitors on EHS standards, expectations, and company guidelines within manufacturing areas.

 - Advise teams on EHS requirements and best practices in manufacturing environments.

 - Lead and participate in internal audits, inspections, and compliance activities.

 - Contribute to the implementation of industry best practices and continuous improvement initiatives.


Minimum Education and Experience Required for the Role


 - University degree in Biotechnology, Chemistry, Engineering, or a related scientific discipline.

 - Degree-level education, preferably in a scientific, technical, or engineering field.

 - At least 1 year of experience in a Health &amp; Safety role within a regulated industry.

 - Understanding of biotechnology manufacturing processes, including relevant methods, techniques, and equipment.

 - Strong written, verbal, and interpersonal communication skills.

 - Proactive mindset with sound judgment and decision-making abilities.

 - Demonstrated ability to work independently, solve problems effectively, and manage multiple priorities in a fast-paced environment.

 - Candidates without direct EHS experience are encouraged to apply if they possess a relevant educational background, laboratory safety experience, and a strong interest in building a career within EHS.


What We Offer


 - The opportunity to work alongside talented colleagues on meaningful projects that improve patients’ lives.

 - A chance to be part of a global, innovative, and rapidly growing biopharmaceutical company.

 - An international and inclusive culture that values diversity, collaboration, and respect.

 - A positive, flexible, and forward-thinking work environment.

 - Ongoing opportunities for personal development and internal career growth.

 - Company social events, celebrations, and team-building activities.

 - Excellent on-site canteen and coffee house facilities.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facilities.

 - Transportation grant supporting eco-friendly commuting options for full-time employees.

 - Home internet support for full-time employees.


Why Alvotech?

At Alvotech, we are passionate about improving lives by increasing access to affordable biologic medicines. As a purpose-driven organization, we foster an inclusive environment where curiosity, innovation, and simplicity are valued. We empower our employees to take ownership of their careers, embrace meaningful challenges, and thrive in a fast-moving and collaborative setting.

True to our Icelandic roots, we are committed to integrity, fairness, gender equality, and respect for diverse perspectives. We believe that bringing together talented individuals from different backgrounds enables us to deliver exceptional results for our partners and patients around the world.

Join us in shaping a healthier future and creating greater access to life-changing biologic medicines worldwide.




EHS Specialist

We are seeking a Master Data Lead to drive the integrity, accuracy, consistency, and governance of critical business data across SAP and associated systems. This role plays a key part in ensuring high-quality master data that supports efficient operations, accurate financial reporting, effective procurement processes, and strong business decision-making.
Working closely with teams across Procurement, Finance, Operations, and IT, you will act as the organization's subject matter expert for master data quality and governance. You will lead initiatives that strengthen data standards, improve processes, and enhance data reliability across the business. &nbsp;
Key Responsibilities:
Data Quality Management
<ul>
<li>Own and champion data quality standards across SAP and associated business systems.</li>
<li>Monitor, assess, and improve the accuracy, completeness, consistency, and integrity of master data.</li>
<li>Identify recurring data issues and implement sustainable solutions to prevent reoccurrence.</li>
<li>Conduct regular reviews and audits to ensure adherence to data standards and policies.</li>
<li>Establish and monitor data quality metrics, reporting on trends, risks, and improvement opportunities.</li>
<li>Investigate root causes of data-related issues and coordinate corrective actions with relevant stakeholders.</li>
</ul>
 Master Data Governance
<ul>
<li>Maintain governance frameworks for key master data domains.</li>
<li>Define and document data standards, business rules, approval requirements, and maintenance procedures.</li>
<li>Ensure appropriate controls exist for the creation, modification, and retirement of master data.</li>
<li>Act as the custodian of master data policies and governance practices.</li>
<li>Facilitate data stewardship across business functions by defining roles, responsibilities, and accountability.</li>
</ul>
Procurement Data Management
<ul>
<li>Ensure the quality and integrity of vendor master data.</li>
<li>Oversee material categorization structures to support procurement and reporting requirements.</li>
<li>Maintain governance over pricing information and supplier price lists.</li>
<li>Identify and resolve data issues impacting purchasing, sourcing, inventory management, and supplier performance.</li>
</ul>

Finance Data Management
<ul>
<li>Support the accuracy and control of key financial master data, including:</li>
<li>General Ledger (G/L) accounts, Cost centers, Financial hierarchies, Approval workflows, Organizational and reporting structures</li>
<li>Partner with Finance to maintain data that supports reporting, budgeting, forecasting, and compliance activities.</li>
<li>Contribute to strong financial controls through effective master data management.</li>
</ul>
Continuous Improvement
<ul>
<li>Drive initiatives that improve data quality, reduce manual workarounds, and increase process efficiency.</li>
<li>Support ERP enhancements, system upgrades, and transformation projects from a data quality perspective.</li>
<li>Recommend process improvements and automation opportunities that enhance data integrity.</li>
<li>Promote a culture of accountability and ownership for data quality across the business.&nbsp;</li>
</ul>
You will collaborate closely with:
<ul>
<li>Finance</li>
<li>Procurement</li>
<li>Operations</li>
<li>IT / ERP Support Teams</li>
<li>Business Process Owners</li>
<li>External System Vendors (where applicable)</li>
</ul>
What Success Looks Like
<ul>
<li>Reduced recurring master data issues.</li>
<li>Improved master data quality across key business domains.</li>
<li>Reduced manual intervention resulting from poor data quality.</li>
<li>Increased reliability of operational and financial reporting.</li>
<li>Strong compliance with governance and approval requirements.</li>
<li>Greater stakeholder confidence in business data.</li>
</ul>
Qualifications and Competencies: 
<ul>
<li>Bachelor's degree in Finance, Accounting, Business Administration, Engineering or a related field.</li>
<li>Expertise in Data Quality Management and Master Data Governance.</li>
<li>Strong SAP knowledge.</li>
<li>Understanding of financial and procurement processes.</li>
<li>Experience in root cause analysis and process improvement.</li>
<li>Ability to influence stakeholders across multiple business functions.</li>
<li>Strong attention to detail and problem-solving skills.</li>
<li>Continuous improvement mindset with a focus on delivering sustainable outcomes.</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>Internet at home for full-time employees.</li>
</ul>


We are seeking a Master Data Lead to drive the integrity, accuracy, consistency, and governance of critical business data across SAP and associated systems. This role plays a key part in ensuring high-quality master data that supports efficient operations, accurate financial reporting, effective procurement processes, and strong business decision-making.

Working closely with teams across Procurement, Finance, Operations, and IT, you will act as the organization's subject matter expert for master data quality and governance. You will lead initiatives that strengthen data standards, improve processes, and enhance data reliability across the business.



Key Responsibilities:

Data Quality Management


 - Own and champion data quality standards across SAP and associated business systems.

 - Monitor, assess, and improve the accuracy, completeness, consistency, and integrity of master data.

 - Identify recurring data issues and implement sustainable solutions to prevent reoccurrence.

 - Conduct regular reviews and audits to ensure adherence to data standards and policies.

 - Establish and monitor data quality metrics, reporting on trends, risks, and improvement opportunities.

 - Investigate root causes of data-related issues and coordinate corrective actions with relevant stakeholders.



Master Data Governance


 - Maintain governance frameworks for key master data domains.

 - Define and document data standards, business rules, approval requirements, and maintenance procedures.

 - Ensure appropriate controls exist for the creation, modification, and retirement of master data.

 - Act as the custodian of master data policies and governance practices.

 - Facilitate data stewardship across business functions by defining roles, responsibilities, and accountability.


Procurement Data Management


 - Ensure the quality and integrity of vendor master data.

 - Oversee material categorization structures to support procurement and reporting requirements.

 - Maintain governance over pricing information and supplier price lists.

 - Identify and resolve data issues impacting purchasing, sourcing, inventory management, and supplier performance.




Finance Data Management


 - Support the accuracy and control of key financial master data, including:

 - General Ledger (G/L) accounts, Cost centers, Financial hierarchies, Approval workflows, Organizational and reporting structures

 - Partner with Finance to maintain data that supports reporting, budgeting, forecasting, and compliance activities.

 - Contribute to strong financial controls through effective master data management.


Continuous Improvement


 - Drive initiatives that improve data quality, reduce manual workarounds, and increase process efficiency.

 - Support ERP enhancements, system upgrades, and transformation projects from a data quality perspective.

 - Recommend process improvements and automation opportunities that enhance data integrity.

 - Promote a culture of accountability and ownership for data quality across the business.



You will collaborate closely with:


 - Finance

 - Procurement

 - Operations

 - IT / ERP Support Teams

 - Business Process Owners

 - External System Vendors (where applicable)


What Success Looks Like


 - Reduced recurring master data issues.

 - Improved master data quality across key business domains.

 - Reduced manual intervention resulting from poor data quality.

 - Increased reliability of operational and financial reporting.

 - Strong compliance with governance and approval requirements.

 - Greater stakeholder confidence in business data.


Qualifications and Competencies: 


 - Bachelor's degree in Finance, Accounting, Business Administration, Engineering or a related field.

 - Expertise in Data Quality Management and Master Data Governance.

 - Strong SAP knowledge.

 - Understanding of financial and procurement processes.

 - Experience in root cause analysis and process improvement.

 - Ability to influence stakeholders across multiple business functions.

 - Strong attention to detail and problem-solving skills.

 - Continuous improvement mindset with a focus on delivering sustainable outcomes.


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.

 - Internet at home for full-time employees.




Master Data Lead

QC Bioassay Principal Scientist

We are searching for a motivated and detail oriented QC Bioassay Principal Scientist to support quality control testing activities for biosimilars. This role is responsible for executing and troubleshooting cell based potency assay, ensuring compliance with regulatory and GMP standards, and contributing to continuous improvement initiatives within the QC laboratory.

Key Responsibility:&nbsp;
<ul>
<li>Independently accountable for completing assigned tasks and deliverables, while receiving direction and assignments from a supervisor.</li>
</ul>
<ul>
<li>Demonstrates in-depth knowledge and proficiency in Bioassay (cell-based potency assays, ELISA, binding assays etc).</li>
</ul>
<ul>
<li>Executing and troubleshooting cell based&nbsp;potency assays. Provide good technical input for Invalid assays investigations.</li>
</ul>
<ul>
<li>Executes non‑routine activities, including deviations, change controls, CAPAs, and related investigation actions.</li>
</ul>
<ul>
<li>Prepare testing protocols and reports, and review laboratory and cell bank documentation.</li>
</ul>
<ul>
<li>Analyze, interpret, and document experimental data in line with ALCOA+ data integrity standards.&nbsp;</li>
</ul>
<ul>
<li>Support qualification and optimization of critical reagents (e.g., reference materials) and technical&nbsp;troubleshooting&nbsp;</li>
</ul>
<ul>
<li>Challenges and decisions are addressed collaboratively with cross‑functional teams, with solutions developed in partnership with the supervisor and other team members.</li>
</ul>
<ul>
<li>Possesses expert knowledge of cell‑based assays, including relevant methods, techniques and associated procedural and process requirements.</li>
</ul>
<ul>
<li>Provide technical training and support to team members and ensure proper understanding of laboratory methods and procedural requirements as needed.</li>
</ul>
<ul>
<li>Support technology transfer and validation activities by contributing to the preparation and review of technical documents.</li>
</ul>
<ul>
<li>Personally, authors and reviews key analytical sections related to potency methods within regulatory submissions, as well as responses to queries from health authorities and external partners.</li>
</ul>
<ul>
<li>Requires familiarity with ALCOA+ principles to uphold data integrity in regulated environments, ensuring records are accurate, traceable, and audit ready.</li>
</ul>

Qualifications and experience:&nbsp;
<ul>
<li>Master&rsquo;s degree or&nbsp;Ph.D&nbsp;in Biochemistry, Biotechnology, Biology, or&nbsp;a&nbsp;related&nbsp;field.&nbsp;</li>
</ul>
<ul>
<li>Minimum 8 years previous experience with Potency/ cell-based assays. Knowledge and experience of working to GMP standards.</li>
</ul>
<ul>
<li>Ability to work both independently and collaboratively in a fast-paced environment&nbsp;</li>
</ul>
<ul>
<li>Communication skills: Excellent written and verbal communication skills&nbsp;</li>
</ul>
<ul>
<li>Computer literacy: Proficient in use of a PC and common Microsoft packages such as Word, Excel.</li>
<li>Excellent command of the English language, both written and verbal.</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>
<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


QC Bioassay Principal Scientist



We are searching for a motivated and detail oriented QC Bioassay Principal Scientist to support quality control testing activities for biosimilars. This role is responsible for executing and troubleshooting cell based potency assay, ensuring compliance with regulatory and GMP standards, and contributing to continuous improvement initiatives within the QC laboratory.



Key Responsibility:



 - Independently accountable for completing assigned tasks and deliverables, while receiving direction and assignments from a supervisor.



 - Demonstrates in-depth knowledge and proficiency in Bioassay (cell-based potency assays, ELISA, binding assays etc).



 - Executing and troubleshooting cell based
potency assays. Provide good technical input for Invalid assays investigations.



 - Executes non‑routine activities, including deviations, change controls, CAPAs, and related investigation actions.



 - Prepare testing protocols and reports, and review laboratory and cell bank documentation.



 - Analyze, interpret, and document experimental data in line with ALCOA+ data integrity standards.




 - Support qualification and optimization of critical reagents (e.g., reference materials) and technical
troubleshooting




 - Challenges and decisions are addressed collaboratively with cross‑functional teams, with solutions developed in partnership with the supervisor and other team members.



 - Possesses expert knowledge of cell‑based assays, including relevant methods, techniques and associated procedural and process requirements.



 - Provide technical training and support to team members and ensure proper understanding of laboratory methods and procedural requirements as needed.



 - Support technology transfer and validation activities by contributing to the preparation and review of technical documents.



 - Personally, authors and reviews key analytical sections related to potency methods within regulatory submissions, as well as responses to queries from health authorities and external partners.



 - Requires familiarity with ALCOA+ principles to uphold data integrity in regulated environments, ensuring records are accurate, traceable, and audit ready.




Qualifications and experience:



 - Master’s degree or
Ph.D
in Biochemistry, Biotechnology, Biology, or
a
related
field.




 - Minimum 8 years previous experience with Potency/ cell-based assays. Knowledge and experience of working to GMP standards.



 - Ability to work both independently and collaboratively in a fast-paced environment




 - Communication skills: Excellent written and verbal communication skills




 - Computer literacy: Proficient in use of a PC and common Microsoft packages such as Word, Excel.

 - Excellent command of the English language, both written and verbal.


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

QC Bioassay Principal Scientist

Nowe oferty

Starszy Technik Produkcji Aseptycznej

Specjalista ds. EHS

Kierownik ds. danych głównych

Główny naukowiec ds. badań biologicznych QC

QC ranns&oacute;knarstofut&aelig;knir / QC Laboratory Technician
Vi&eth; leitum a&eth; n&aacute;kv&aelig;mum og &aacute;rei&eth;anlegum QC ranns&oacute;knarstofut&aelig;kni me&eth; sterka &aacute;herslu &aacute; g&aelig;&eth;i og &ouml;ryggi til a&eth; sty&eth;ja vi&eth; daglegan rekstur g&aelig;&eth;ast&yacute;ringarranns&oacute;knarstofu. Starfi&eth; felur &iacute; s&eacute;r a&eth; vi&eth;halda hreinu, skipul&ouml;g&eth;u og GMP-samr&aelig;mdu vinnuumhverfi og tryggja a&eth; starfsemi ranns&oacute;knarstofunnar uppfylli vi&eth;eigandi g&aelig;&eth;akr&ouml;fur og regluger&eth;ir.

[English]
​QC Laboratory Technician
We are looking for a detail-oriented and reliable QC Laboratory Technician with a strong commitment to quality and safety to support daily Quality Control laboratory operations by maintaining a clean, organized, and GMP-compliant environment.
 &nbsp; &nbsp; Scope and Responsibilities: 
<ul>
<li>Conduct routine cleaning and facility sanitation measures.</li>
<li>Conduct verification and upkeep of laboratory and equipment, perform relocation of qualified equipment.</li>
<li>Prepare reagents and solutions following set instructions.</li>
<li>Care, wash and organise laboratory glassware.</li>
<li>Independently manage laboratory inventory, including performing stock checks and raising purchase requests.</li>
<li>Reviewing laboratory logbooks to maintain Good Laboratory Practices (GLP).</li>
<li>Maintaining cleanliness of assigned lab areas.</li>
<li>Identifying improvement opportunities for workflow or lab organization.</li>
<li>Support change management activities and other related tasks.

Qualifications and skills:
</li>
<li>Technician or Bachelor degree of Chemistry, Biology, Pharmaceutical Sciences or in other relevant fields.</li>
<li>1-3 years of experience is highly desirable.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficient in use of a PC and common Microsoft packages such as Word, Visio, Excel.</li>
<li>Initiative, attention to detail and precise work habits.</li>
<li>Fluent command of the English language, both written and verbal.

What we offer:
</li>
<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


QC rannsóknarstofutæknir / QC Laboratory Technician

Við leitum að nákvæmum og áreiðanlegum QC rannsóknarstofutækni með sterka áherslu á gæði og öryggi til að styðja við daglegan rekstur gæðastýringarrannsóknarstofu. Starfið felur í sér að viðhalda hreinu, skipulögðu og GMP-samræmdu vinnuumhverfi og tryggja að starfsemi rannsóknarstofunnar uppfylli viðeigandi gæðakröfur og reglugerðir.



[English]

​QC Laboratory Technician

We are looking for a detail-oriented and reliable QC Laboratory Technician with a strong commitment to quality and safety to support daily Quality Control laboratory operations by maintaining a clean, organized, and GMP-compliant environment.



 
 Scope and Responsibilities: 


 - Conduct routine cleaning and facility sanitation measures.

 - Conduct verification and upkeep of laboratory and equipment, perform relocation of qualified equipment.

 - Prepare reagents and solutions following set instructions.

 - Care, wash and organise laboratory glassware.

 - Independently manage laboratory inventory, including performing stock checks and raising purchase requests.

 - Reviewing laboratory logbooks to maintain Good Laboratory Practices (GLP).

 - Maintaining cleanliness of assigned lab areas.

 - Identifying improvement opportunities for workflow or lab organization.

 - Support change management activities and other related tasks.



Qualifications and skills:


 - Technician or Bachelor degree of Chemistry, Biology, Pharmaceutical Sciences or in other relevant fields.

 - 1-3 years of experience is highly desirable.

 - Excellent written and verbal communication skills.

 - Proficient in use of a PC and common Microsoft packages such as Word, Visio, Excel.

 - Initiative, attention to detail and precise work habits.

 - Fluent command of the English language, both written and verbal.



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