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

Website

Facebook

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LinkedIn

Activity

Commute

Food / meal at work

Entertainment

Work environment

Hefur &thorn;&uacute; gott auga fyrir sm&aacute;atri&eth;um og &aacute;huga &aacute; g&aelig;&eth;am&aacute;lum &iacute; lyfja- og l&iacute;ft&aelig;knii&eth;na&eth;i? Vi&eth; erum a&eth; leita a&eth; metna&eth;arfullum Batch Record Reviewer til a&eth; tryggja a&eth; framlei&eth;sla okkar uppfylli strangar regluger&eth;arkr&ouml;fur og h&aelig;stu g&aelig;&eth;asta&eth;la.
&nbsp;
(English)
&nbsp;
Are you detail-oriented and passionate about quality assurance in the pharmaceutical or biotech industry? We are seeking a dedicated Batch Record Reviewer to ensure compliance with regulatory standards and maintain the highest quality in our production processes. Scope &amp; Responsibilities:
<ul>
<li>Review and approve batch records for accuracy and completeness.</li>
<li>Ensure compliance with cGMP regulations and internal SOPs.</li>
<li>Collaborate with cross-functional teams to resolve discrepancies.</li>
<li>Participate in audits and inspections as needed.</li>
</ul>
&nbsp;
Qualifications and skills:
<ul>
<li>Bachelor&rsquo;s degree in a scientific discipline or equivalent experience.</li>
<li>Experience in batch record review or quality assurance in a regulated environment is a plus.</li>
<li>Strong attention to detail and analytical skills.</li>
<li>Excellent communication and teamwork abilities.</li>
</ul>
&nbsp;
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

Alvotech hf


Hefur þú gott auga fyrir smáatriðum og áhuga á gæðamálum í lyfja- og líftækniiðnaði? Við erum að leita að metnaðarfullum Batch Record Reviewer til að tryggja að framleiðsla okkar uppfylli strangar reglugerðarkröfur og hæstu gæðastaðla.




(English)




Are you detail-oriented and passionate about quality assurance in the pharmaceutical or biotech industry? We are seeking a dedicated Batch Record Reviewer to ensure compliance with regulatory standards and maintain the highest quality in our production processes.

Scope &amp; Responsibilities:


 - Review and approve batch records for accuracy and completeness.

 - Ensure compliance with cGMP regulations and internal SOPs.

 - Collaborate with cross-functional teams to resolve discrepancies.

 - Participate in audits and inspections as needed.





Qualifications and skills:


 - Bachelor’s degree in a scientific discipline or equivalent experience.

 - Experience in batch record review or quality assurance in a regulated environment is a plus.

 - Strong attention to detail and analytical skills.

 - Excellent communication and teamwork abilities.





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

Active

Batch Record Reviewer

Overview of role:
At Alvotech, we are driven by a shared purpose: improving lives by increasing access to affordable biologic medicines worldwide. As a fast-growing global biotechnology company, we foster a collaborative, inclusive, and innovative environment where talented professionals can make a meaningful impact.
We are looking for an experienced MST Compliance Support Specialist to join our Manufacturing Science &amp; Technology (MST) team. In this role, you will support MST quality and compliance activities by overseeing quality events, investigations, CAPAs, and change controls, while ensuring timely resolution and regulatory compliance. You will serve as the key compliance liaison, support inspections and audits, and drive standardized quality practices across the departments within Manufacturing, Science &amp; Technology. &nbsp;
Key Responsibilities:
<ul>
<li>Lead and establish MST quality record and quality event management strategies, including change controls, manufacturing investigations, deviations, CAPAs, and related processes.</li>
<li>Monitor, track, and drive timely progression and closure of quality events based on priority and criticality.</li>
<li>Standardize quality event management processes and ensure a harmonized approach across MST teams.</li>
<li>Act as the primary point of contact for compliance-related matters within MST.</li>
<li>Collaborate closely with internal stakeholders, Operational QA, and external Quality teams to resolve compliance issues and support business objectives.</li>
<li>Represent MST in quality and governance review boards, including deviation, complaint, investigation, and control strategy forums.</li>
<li>Support regulatory inspections, quality audits, and due diligence activities.</li>
<li>Review MST documentation to ensure compliance with cGMP requirements, internal procedures, and regulatory expectations.</li>
<li>Contribute to the development and revision of SOPs, training materials, and controlled documentation.</li>
<li>Provide oversight of outsourced MST activities and maintain compliance visibility across sites and partners.</li>
</ul>
&nbsp;
Required Qualifications
<ul>
<li>Bachelor's or Master's degree in Biotechnology, Life Sciences, Pharmacy, or a related scientific discipline.</li>
<li>Robust experience in authoring Scientific and Quality Management System related documents</li>
<li>5+ years of experience in Quality, Compliance, or related roles within the biopharmaceutical industry.</li>
<li>Excellent stakeholder management, communication, and cross-functional collaboration skills.</li>
<li>Ability to work independently, manage multiple priorities, and drive compliance initiatives in a dynamic environment.</li>
</ul>
&nbsp;
Preferred Skills
<ul>
<li>Experience managing quality events, CAPAs, change controls, and investigations.</li>
<li>Proven ability to influence stakeholders and lead compliance-related improvement initiatives.</li>
<li>Strong analytical mindset with excellent problem-solving capabilities</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.&nbsp;</li>
</ul>


Overview of role:

At Alvotech, we are driven by a shared purpose: improving lives by increasing access to affordable biologic medicines worldwide. As a fast-growing global biotechnology company, we foster a collaborative, inclusive, and innovative environment where talented professionals can make a meaningful impact.

We are looking for an experienced MST Compliance Support Specialist to join our Manufacturing Science &amp; Technology (MST) team. In this role, you will support MST quality and compliance activities by overseeing quality events, investigations, CAPAs, and change controls, while ensuring timely resolution and regulatory compliance. You will serve as the key compliance liaison, support inspections and audits, and drive standardized quality practices across the departments within Manufacturing, Science &amp; Technology.



Key Responsibilities:


 - Lead and establish MST quality record and quality event management strategies, including change controls, manufacturing investigations, deviations, CAPAs, and related processes.

 - Monitor, track, and drive timely progression and closure of quality events based on priority and criticality.

 - Standardize quality event management processes and ensure a harmonized approach across MST teams.

 - Act as the primary point of contact for compliance-related matters within MST.

 - Collaborate closely with internal stakeholders, Operational QA, and external Quality teams to resolve compliance issues and support business objectives.

 - Represent MST in quality and governance review boards, including deviation, complaint, investigation, and control strategy forums.

 - Support regulatory inspections, quality audits, and due diligence activities.

 - Review MST documentation to ensure compliance with cGMP requirements, internal procedures, and regulatory expectations.

 - Contribute to the development and revision of SOPs, training materials, and controlled documentation.

 - Provide oversight of outsourced MST activities and maintain compliance visibility across sites and partners.





Required Qualifications


 - Bachelor's or Master's degree in Biotechnology, Life Sciences, Pharmacy, or a related scientific discipline.

 - Robust experience in authoring Scientific and Quality Management System related documents

 - 5+ years of experience in Quality, Compliance, or related roles within the biopharmaceutical industry.

 - Excellent stakeholder management, communication, and cross-functional collaboration skills.

 - Ability to work independently, manage multiple priorities, and drive compliance initiatives in a dynamic environment.





Preferred Skills


 - Experience managing quality events, CAPAs, change controls, and investigations.

 - Proven ability to influence stakeholders and lead compliance-related improvement initiatives.

 - Strong analytical mindset with excellent problem-solving capabilities


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

MST Compliance Support Specialist

QA Specialist - Product Testing Review
We are seeking a QA Specialist to join our QA Product Testing Review team. In this role, the candidate will independently review and approve laboratory documentation supporting product release, in-process, and stability testing in accordance with GDP requirements in a GMP-regulated pharmaceutical or biopharmaceutical environment.
&nbsp;
Scope and Responsibilities:
<ul>
<li>Review and complete laboratory documentation (support stability, product in-process and release testing)&nbsp;.</li>
<li>Inform about review issues.&nbsp;</li>
<li>Provide technical support where required.</li>
<li>Being able to work in accordance with GMP practices, conducting all activities in a compliant manner.</li>
<li>Provide expertise in selected analytical techniques and thorough understanding and overview of all analytical methods applied for product testing and stability testing.&nbsp;</li>
<li>Being aware of and comply with Alvotech&rsquo;s current EHS policies.</li>
<li>Support deviations and investigations as required.</li>
<li>Provide support during inspections as required.&nbsp;</li>
<li>Being independent in assignments. Routinely lead projects and/or supervise small or medium teams of technicians or admin.&nbsp;</li>
<li>Perform both routine tasks within procedures and processes and non-routine tasks. Take part in large projects.&nbsp;</li>
<li>Challenges and decisions are discussed, made and solved in cooperation with supervisor/other employees.&nbsp;</li>
<li>Can make adjustments/changes to procedures, processes and projects.&nbsp;</li>
<li>Can have financial impact through decision making.&nbsp;</li>
<li>Demonstrate expert knowledge within field of expertise such as methods, techniques and equipment as well as relevant procedural/process knowledge.&nbsp;</li>
<li>Being often an advisory to other less experienced employees.&nbsp;</li>
<li>Apply good documentation practices when completing records.&nbsp;</li>
</ul>
Minimum education and experience requirements:
<ul>
<li>Education and experience: University degree in a relevant scientific discipline and minimum 1-3 years of relevant experience in pharmaceutical or biopharmaceutical sector.&nbsp;</li>
<li>Communication skills: Excellent written and verbal communication skills, coordination abilities and good team skills.</li>
<li>Computer literacy: Proficient in use of a PC and common Microsoft packages such as Word, Excel and PowerPoint.</li>
</ul>
&nbsp;
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


QA Specialist - Product Testing Review

We are seeking a QA Specialist to join our QA Product Testing Review team. In this role, the candidate will independently review and approve laboratory documentation supporting product release, in-process, and stability testing in accordance with GDP requirements in a GMP-regulated pharmaceutical or biopharmaceutical environment.




Scope and Responsibilities:


 - Review and complete laboratory documentation (support stability, product in-process and release testing)
.

 - Inform about review issues.


 - Provide technical support where required.

 - Being able to work in accordance with GMP practices, conducting all activities in a compliant manner.

 - Provide expertise in selected analytical techniques and thorough understanding and overview of all analytical methods applied for product testing and stability testing.


 - Being aware of and comply with Alvotech’s current EHS policies.

 - Support deviations and investigations as required.

 - Provide support during inspections as required.


 - Being independent in assignments. Routinely lead projects and/or supervise small or medium teams of technicians or admin.


 - Perform both routine tasks within procedures and processes and non-routine tasks. Take part in large projects.


 - Challenges and decisions are discussed, made and solved in cooperation with supervisor/other employees.


 - Can make adjustments/changes to procedures, processes and projects.


 - Can have financial impact through decision making.


 - Demonstrate expert knowledge within field of expertise such as methods, techniques and equipment as well as relevant procedural/process knowledge.


 - Being often an advisory to other less experienced employees.


 - Apply good documentation practices when completing records.



Minimum education and experience requirements:


 - Education and experience: University degree in a relevant scientific discipline and minimum 1-3 years of relevant experience in pharmaceutical or biopharmaceutical sector.


 - Communication skills: Excellent written and verbal communication skills, coordination abilities and good team skills.

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





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





QA Specialist - Product Testing Review

We are looking for a Scientist in Quality Control Product Testing team at Alvotech. The position plays a vital role by participating in the quality control and release of products manufactured at Alvotech. We are looking for an individual that has a positive attitude, embraces challenges, is flexible and adaptive, and shares our values of team spirit and team efforts.
Scope and responsibility:
<ul>
<li>Performs routine analytical testing with advanced analytical techniques such as LC (APAC, SEC, CEX, N-glycan, Peptide mapping) and CE (CE-SDS, CIEF) as well as compendial methods support manufacturing operations.</li>
<li>Participate in the creation, review and maintenance of quality documents within Alvotech.</li>
<li>Contributes to other documentation reviews and/or updates within the Quality management system.</li>
</ul>
<ul>
<li>Support the investigations for quality issues such as Invalid assay, OOS/OOT/OOE results.</li>
<li>Support in change control, CAPAs, Document change controls.</li>
<li>Performs both routine tasks within procedures, processes and non-routine tasks such as support Invalid assays, change controls, document updates and CAPAs.</li>
</ul>
<ul>
<li>Performing routine cleaning, verification, stock checks, and upkeep of laboratory and equipment</li>
</ul>
<ul>
<li>Performing activities required to support testing, e.g., buffer preparation</li>
</ul>
Job requirements:
<ul>
<li>Bachelor&rsquo;s or master&rsquo;s Degree in a relevant scientific discipline and at least 1-5 years of relevant experience in the pharmaceutical or biopharmaceutical sector.</li>
<li>Proficient in using a PC and common Microsoft packages such as Word and Excel.</li>
<li>Understanding and review of electronic data from instrument software.</li>
<li>Knowledge of Good Manufacturing Practices (GMP) and documentation Rules is an asset.</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


We are looking for a Scientist in Quality Control Product Testing team at Alvotech. The position plays a vital role by participating in the quality control and release of products manufactured at Alvotech. We are looking for an individual that has a positive attitude, embraces challenges, is flexible and adaptive, and shares our values of team spirit and team efforts.

Scope and responsibility:


 - Performs routine analytical testing with advanced analytical techniques such as LC (APAC, SEC, CEX, N-glycan, Peptide mapping) and CE (CE-SDS, CIEF) as well as compendial methods support manufacturing operations.

 - Participate in the creation, review and maintenance of quality documents within Alvotech.

 - Contributes to other documentation reviews and/or updates within the Quality management system.



 - Support the investigations for quality issues such as Invalid assay, OOS/OOT/OOE results.

 - Support in change control, CAPAs, Document change controls.

 - Performs both routine tasks within procedures, processes and non-routine tasks such as support Invalid assays, change controls, document updates and CAPAs.



 - Performing routine cleaning, verification, stock checks, and upkeep of laboratory and equipment



 - Performing activities required to support testing, e.g., buffer preparation


Job requirements:


 - Bachelor’s or master’s Degree in a relevant scientific discipline and at least 1-5 years of relevant experience in the pharmaceutical or biopharmaceutical sector.

 - Proficient in using a PC and common Microsoft packages such as Word and Excel.

 - Understanding and review of electronic data from instrument software.

 - Knowledge of Good Manufacturing Practices (GMP) and documentation Rules is an asset.


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 Analytical Scientist

Latest jobs

At&nbsp;Alvotech, we are driven by a clear mission: improving lives by increasing access to high-quality, affordable biologic medicines. As we continue to grow globally, we are looking for a Senior Specialist, Manufacturing Operations (Control Operations) to join our team and play a key role in maintaining GMP compliance, manufacturing oversight, and continuous improvement across our operations.&nbsp;
If you thrive in a fast-paced GMP environment, enjoy problem-solving, and are passionate about quality and compliance, we would love to hear from you.&nbsp; &nbsp;
About the role:&nbsp;&nbsp; &nbsp; As a Senior Specialist, Manufacturing Operations, you will serve as a key contributor to quality and compliance activities within our manufacturing operations. You will collaborate closely with cross-functional teams to ensure&nbsp;inspection&nbsp;readiness, drive investigations, and support operational excellence.&nbsp; &nbsp;
Key Responsibilities&nbsp;
<ul>
<li>
Lead and manage investigations, ensuring&nbsp;timely&nbsp;closure of quality records in line with established KPIs.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Handle and support investigations, CAPAs, effectiveness checks, and change controls, ensuring&nbsp;timely&nbsp;completion and compliance with GMP requirements.&nbsp;
</li>
</ul>
<ul>
<li>
Provide&nbsp;expertise&nbsp;for Environmental Monitoring (EM) excursions, collaborating with QC Microbiology and Sterility Assurance teams.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Prepare Cell Bank Stability Plans and Annual Cell Bank Stability Reports.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Perform audit trail reviews of manufacturing systems and support closure of audit reports.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Provide technical oversight during manufacturing operations, troubleshooting&nbsp;issues&nbsp;and reviewing quality documentation.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Deliver GMP and GDP training and awareness sessions&nbsp;to&nbsp;manufacturing personnel.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Maintain and update operational procedures and system-related SOPs.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Develop and analyze quality metrics,&nbsp;identifying&nbsp;trends&nbsp;and&nbsp;supporting&nbsp;risk mitigation strategies.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Track and manage quality records to ensure regulatory compliance.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Maintain&nbsp;inspection&nbsp;readiness of manufacturing suites and equipment.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Participate in risk assessments, root cause analyses, and implementation of effective corrective actions.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Partner with Manufacturing, MSAT, QC, and QA teams to drive compliance and operational excellence.&nbsp;&nbsp;
</li>
</ul>
<ul>
<li>
Contribute to continuous improvement initiatives that enhance quality, efficiency, and compliance.&nbsp;
</li>
</ul>
&nbsp;
Qualifications&nbsp;
<ul>
<li>
Bachelor&rsquo;s or master&rsquo;s&nbsp;degree in chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or related&nbsp;field.&nbsp;
</li>
</ul>
<ul>
<li>
Minimum 5&nbsp;years experience&nbsp;in Downstream&nbsp;manufacuring&nbsp;roles.&nbsp;
</li>
</ul>
<ul>
<li>
Strong understanding of GMP requirements within pharmaceutical or biopharmaceutical manufacturing environments.&nbsp;
</li>
</ul>
<ul>
<li>
Excellent written and verbal communication skills in English.&nbsp;
</li>
</ul>
<ul>
<li>
Exceptional organizational skills with a keen eye for detail.&nbsp;
</li>
</ul>
<ul>
<li>
Proactive, solution-oriented mindset and strong collaboration abilities.&nbsp; &nbsp;
</li>
</ul>
What we offer:&nbsp;&nbsp;
<ul>
<li>
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.&nbsp;
</li>
</ul>
<ul>
<li>
The chance to be a part of a global and fast-growing company.&nbsp;
</li>
</ul>
<ul>
<li>
An international work culture that encourages diversity,&nbsp;collaboration&nbsp;and inclusion.&nbsp;
</li>
</ul>
<ul>
<li>
Positive, flexible, and innovative work environment.&nbsp;
</li>
</ul>
<ul>
<li>
Support for personal growth and internal career development.&nbsp;
</li>
</ul>
<ul>
<li>
Company social events and milestone celebrations.&nbsp;
</li>
</ul>
<ul>
<li>
Excellent in-house canteen and coffee house.&nbsp;
</li>
</ul>
<ul>
<li>
Exercise and wellbeing support for full-time employees.&nbsp;
</li>
</ul>
<ul>
<li>
On-site shower facility.&nbsp;
</li>
</ul>
<ul>
<li>
Transportation&nbsp;grant&nbsp;towards eco-friendly modes of travel for full-time employees.&nbsp;
</li>
</ul>
<ul>
<li>
Internet at home for full-time employees.&nbsp;&nbsp; &nbsp;
</li>
</ul>
Why&nbsp;Alvotech&nbsp;:&nbsp; &nbsp; At&nbsp;Alvotech, we are passionate about improving lives by increasing access to affordable biologics.&nbsp;We&rsquo;re&nbsp;purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity,&nbsp;ingenuity&nbsp;and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful&nbsp;work&nbsp;and empowered to succeed in an agile environment.&nbsp; &nbsp; 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.&nbsp;


At
Alvotech, we are driven by a clear mission: improving lives by increasing access to high-quality, affordable biologic medicines. As we continue to grow globally, we are looking for a Senior Specialist, Manufacturing Operations (Control Operations) to join our team and play a key role in maintaining GMP compliance, manufacturing oversight, and continuous improvement across our operations.


If you thrive in a fast-paced GMP environment, enjoy problem-solving, and are passionate about quality and compliance, we would love to hear from you.




About the role:




As a Senior Specialist, Manufacturing Operations, you will serve as a key contributor to quality and compliance activities within our manufacturing operations. You will collaborate closely with cross-functional teams to ensure
inspection
readiness, drive investigations, and support operational excellence.




Key Responsibilities



 - 

Lead and manage investigations, ensuring
timely
closure of quality records in line with established KPIs.






 - 

Handle and support investigations, CAPAs, effectiveness checks, and change controls, ensuring
timely
completion and compliance with GMP requirements.





 - 

Provide
expertise
for Environmental Monitoring (EM) excursions, collaborating with QC Microbiology and Sterility Assurance teams.






 - 

Prepare Cell Bank Stability Plans and Annual Cell Bank Stability Reports.






 - 

Perform audit trail reviews of manufacturing systems and support closure of audit reports.






 - 

Provide technical oversight during manufacturing operations, troubleshooting
issues
and reviewing quality documentation.






 - 

Deliver GMP and GDP training and awareness sessions
to
manufacturing personnel.






 - 

Maintain and update operational procedures and system-related SOPs.






 - 

Develop and analyze quality metrics,
identifying
trends
and
supporting
risk mitigation strategies.






 - 

Track and manage quality records to ensure regulatory compliance.






 - 

Maintain
inspection
readiness of manufacturing suites and equipment.






 - 

Participate in risk assessments, root cause analyses, and implementation of effective corrective actions.






 - 

Partner with Manufacturing, MSAT, QC, and QA teams to drive compliance and operational excellence.






 - 

Contribute to continuous improvement initiatives that enhance quality, efficiency, and compliance.







Qualifications



 - 

Bachelor’s or master’s
degree in chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or related
field.





 - 

Minimum 5
years experience
in Downstream
manufacuring
roles.





 - 

Strong understanding of GMP requirements within pharmaceutical or biopharmaceutical manufacturing environments.





 - 

Excellent written and verbal communication skills in English.





 - 

Exceptional organizational skills with a keen eye for detail.





 - 

Proactive, solution-oriented mindset and strong collaboration abilities.






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.

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 Compliance

About the role We are looking for an experienced HR professional who enjoys working close to the business, understands how people decisions affect performance, and is comfortable operating in a large, complex and highly structured environment. This is a global role, supporting leaders and teams across functions, locations and time zones, with a strong focus on Quality and Regulatory. The final job title may evolve depending on the level and experience of the successful candidate, but the purpose of the role is clear: we need someone who can combine practical HR delivery with business partnering, good judgement, strategic thinking and a genuine interest in how the business works. This is not a purely advisory role, and it is not a role for someone who only wants to work at policy level. We need someone who can think ahead, plan well, challenge constructively and support leaders with practical solutions &mdash; while also being willing to roll up their sleeves and get the work done. That may mean supporting workforce planning one day, coaching a manager through a people matter the next, helping leaders build stronger team culture, and then making sure the right updates are completed accurately in Workday. We are looking for someone who has applied HR in real working environments, not only learned it through textbooks. The right person will understand that HR strategy only works when it can be translated into clear, practical action for leaders, managers and employees. A key part of this role will be helping leaders build and sustain the right culture in their teams. That means making sure managers have the tools, guidance, coaching and support they need to lead well, communicate clearly, develop their people and create an environment where accountability, collaboration and trust are part of everyday work. What you will be doing You will act as a trusted HR partner to leaders and managers across your assigned business areas, helping them translate business priorities into practical people actions. You will support workforce planning, organisational changes, talent discussions, performance management, employee relations, engagement actions, learning and development priorities, leadership capability and day-to-day HR delivery. You will also work closely with colleagues across People &amp; Culture, Talent Acquisition, HR Operations, People Intelligence and other support functions to make sure we are aligned, consistent and easy for the business to work with. Because we operate in a highly regulated environment, compliance, documentation, audit readiness and right-first-time thinking are important. Good HR work in this environment is not only about doing the right thing &mdash; it is also about being able to evidence that the right thing was done, in the right way. You do not need to come from the pharmaceutical industry to be successful in this role. What matters is that you understand how to work in a structured, quality-driven business where good process, sound judgement, documentation and follow-through really matter. This role will suit someone who enjoys variety, can move between strategic discussion and practical delivery, and is comfortable working in a business where priorities can change quickly but accountability, collaboration, learning, culture and quality always matter. &nbsp;


About the role 

We are looking for an experienced HR professional who enjoys working close to the business, understands how people decisions affect performance, and is comfortable operating in a large, complex and highly structured environment. 


This is a global role, supporting leaders and teams across functions, locations and time zones, with a strong focus on Quality and Regulatory. The final job title may evolve depending on the level and experience of the successful candidate, but the purpose of the role is clear: we need someone who can combine practical HR delivery with business partnering, good judgement, strategic thinking and a genuine interest in how the business works. 


This is not a purely advisory role, and it is not a role for someone who only wants to work at policy level. We need someone who can think ahead, plan well, challenge constructively and support leaders with practical solutions — while also being willing to roll up their sleeves and get the work done. That may mean supporting workforce planning one day, coaching a manager through a people matter the next, helping leaders build stronger team culture, and then making sure the right updates are completed accurately in Workday. 


We are looking for someone who has applied HR in real working environments, not only learned it through textbooks. The right person will understand that HR strategy only works when it can be translated into clear, practical action for leaders, managers and employees. 


A key part of this role will be helping leaders build and sustain the right culture in their teams. That means making sure managers have the tools, guidance, coaching and support they need to lead well, communicate clearly, develop their people and create an environment where accountability, collaboration and trust are part of everyday work. 


What you will be doing 

You will act as a trusted HR partner to leaders and managers across your assigned business areas, helping them translate business priorities into practical people actions. 


You will support workforce planning, organisational changes, talent discussions, performance management, employee relations, engagement actions, learning and development priorities, leadership capability and day-to-day HR delivery. You will also work closely with colleagues across People &amp; Culture, Talent Acquisition, HR Operations, People Intelligence and other support functions to make sure we are aligned, consistent and easy for the business to work with. 

Because we operate in a highly regulated environment, compliance, documentation, audit readiness and right-first-time thinking are important. Good HR work in this environment is not only about doing the right thing — it is also about being able to evidence that the right thing was done, in the right way. 


You do not need to come from the pharmaceutical industry to be successful in this role. What matters is that you understand how to work in a structured, quality-driven business where good process, sound judgement, documentation and follow-through really matter. 


This role will suit someone who enjoys variety, can move between strategic discussion and practical delivery, and is comfortable working in a business where priorities can change quickly but accountability, collaboration, learning, culture and quality always matter. 


What will help you succeed here


You will do well in this role if you are:



 - 

Practical, calm and
solutions-focused.





 - 

Comfortable operating in a business where process,
quality
and documentation matter.





 - 

Able to think strategically but happy to get involved in the details.





 - 

Confident enough to challenge, but constructive in how you do it.





 - 

Curious about the business and how people decisions affect performance.





 - 

Interested in culture, leadership and how managers create
strong team
environments.





 - 

Able to turn culture,
engagement
and leadership expectations into practical actions for managers.





 - 

Strong at building relationships across teams,
functions
and locations.





 - 

Organised, reliable and able to follow through.





 - 

A team player who believes HR works best when we
operate
as One Team.





 - 

Energised by a role where no two days are
exactly the same.





 - 

Comfortable working in a global environment where collaboration, clarity and trust are essential.






Why this role matters


Our people decisions directly support the quality,
reliability
and performance of the business. In a complex and highly regulated environment, the way we hire, develop, support, lead and manage people matters — for our teams, our leaders, our compliance obligations and
ultimately for
the patients who rely on our medicines.


This role is a great opportunity for an HR professional who wants to be close to the business, build strong partnerships, help develop leaders, influence culture and make a practical difference every day.



We encourage applicants to apply as early as possible, as Alvotech reserves the right to start the interview process before the application deadline.