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

Instagram

LinkedIn

Activity

Commute

Food / meal at work

Entertainment

Work environment

Vi&eth; leitum a&eth; Associate Scientist &iacute; t&iacute;mabundi&eth; eins &aacute;rs starf til a&eth; leysa af vegna f&aelig;&eth;ingarorlofs.
Associate Scientist &iacute; Quality Control Product Testing teymi gegnir mikilv&aelig;gu hlutverki hj&aacute; Alvotech me&eth; &thorn;&aacute;ttt&ouml;ku &iacute; g&aelig;&eth;aeftirliti og &uacute;tg&aacute;fu &aacute; v&ouml;rum sem framleiddar eru hj&aacute; Alvotech &iacute; 24/7 vaktavinnu. Vi&eth; leitum a&eth; einstaklingi me&eth; j&aacute;kv&aelig;tt hugarfar sem tekur &aacute;skorunum fagnandi, s&yacute;nir sveigjanleika og a&eth;l&ouml;gunarh&aelig;fni og deilir gildum okkar um g&oacute;&eth;a li&eth;sheild og samvinnu.
(English below)
We are seeking an Associate Scientist for a temporary, one‑year position to cover maternity leave
An Associate Scientist in the Quality Control Product Testing team plays a vital role at Alvotech by contributing to the quality control and release of products manufactured at Alvotech during 24/7 operations (shift‑based work schedule). We are looking for an individual with a positive attitude who embraces challenges, is flexible and adaptive, and shares our strong values of teamwork and collaboration.
Scope and responsibility:
<ul>
<li>
Performs routine analytical testing with analytical techniques such as Liquid Chromatography, Capillary electrophoresis, compendial methods and reviews analytical test records to support manufacturing process with limited supervision.
</li>
<li>
Performing routine cleaning, verification, stock checks, and upkeep of laboratory and equipment
</li>
<li>
Performing activities required to support testing, e.g., buffer preparation
</li>
<li>
Participate in the creation and maintenance of quality documents within Alvotech.
</li>
<li>
Contributes to other documentation reviews and/or updates within the Quality management system.
</li>
</ul>
Job requirements:
<ul>
<li>
Bachelor's Degree in a relevant scientific discipline and at least 0-1 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>
Basic 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>

Why Alvotech
We at Alvotech 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


Við leitum að Associate Scientist í tímabundið eins árs starf til að leysa af vegna fæðingarorlofs.

Associate Scientist í Quality Control Product Testing teymi gegnir mikilvægu hlutverki hjá Alvotech með þátttöku í gæðaeftirliti og útgáfu á vörum sem framleiddar eru hjá Alvotech í 24/7 vaktavinnu. Við leitum að einstaklingi með jákvætt hugarfar sem tekur áskorunum fagnandi, sýnir sveigjanleika og aðlögunarhæfni og deilir gildum okkar um góða liðsheild og samvinnu.

(English below)

We are seeking an Associate Scientist for a temporary, one‑year position to cover maternity leave

An Associate Scientist in the Quality Control Product Testing team plays a vital role at Alvotech by contributing to the quality control and release of products manufactured at Alvotech during 24/7 operations (shift‑based work schedule). We are looking for an individual with a positive attitude who embraces challenges, is flexible and adaptive, and shares our strong values of teamwork and collaboration.

Scope and responsibility:


 - 

Performs routine analytical testing with analytical techniques such as Liquid Chromatography, Capillary electrophoresis, compendial methods and reviews analytical test records to support manufacturing process with limited supervision.


 - 

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


 - 

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


 - 

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


 - 

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



Job requirements:


 - 

Bachelor's Degree in a relevant scientific discipline and at least 0-1 years of relevant experience in the pharmaceutical or biopharmaceutical sector.


 - 

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


 - 

Basic 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.





Why Alvotech

We at Alvotech 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

Associate Scientist, QC Product Testing (Fixed‑Term, 1 Year)

Vi&eth; leitum a&eth; tveimur s&eacute;rfr&aelig;&eth;ingum (Scientist) til a&eth; ganga til li&eth;s vi&eth; Quality Control Product Testing teymi&eth; hj&aacute; Alvotech. &THORN;essar st&ouml;&eth;ur gegna lykilhlutverki &iacute; g&aelig;&eth;aeftirliti og losun afur&eth;a sem framleiddar eru hj&aacute; Alvotech. St&ouml;&eth;urnar eru innan Analytical starfseiningarinnar og sty&eth;ja vi&eth; framlei&eth;slu me&eth; h&aacute;&thorn;r&oacute;u&eth;um greiningarapr&oacute;funum og g&aelig;&eth;askj&ouml;lun.
(English below)
We are looking for two Scientists to join the Quality Control Product Testing team at Alvotech. These positions play a vital role in ensuring the quality control and release of products manufactured at Alvotech. The roles are within the Analytical function, supporting manufacturing operations through advanced analytical testing and quality documentation.

The two Scientist positions available are:
<ul>
<li>
Scientist &ndash; Shift Work (24/7 operations)
</li>
<li>
Scientist &ndash; Daytime Work
</li>
</ul>
Both roles involve similar responsibilities, with work schedules adapted to either a shift‑based or standard daytime working pattern.
Scope and responsibilities:
<ul>
<li>
Perform routine analytical testing using advanced analytical techniques such as LC (APAC, SEC, CEX, N-glycan, Peptide mapping) and CE (CE-SDS, CIEF), as well as compendial methods, in support of manufacturing operations.
</li>
<li>
Participate in the creation, review, and maintenance of quality documents within Alvotech.
</li>
<li>
Contribute to documentation reviews and updates within the Quality Management System.
</li>
<li>
Support investigations related to quality issues, including Invalid assay, OOS/OOT/OOE results.
</li>
<li>
Support change controls, CAPAs, and document change controls.
</li>
<li>
Perform both routine tasks within established procedures and non-routine tasks such as investigation support, document updates, and CAPAs.
</li>
<li>
Carry out routine cleaning, verification, stock checks, and general upkeep of laboratory areas and equipment.
</li>
<li>
Perform 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.
</li>
<li>
1&ndash;5 years of relevant experience in the pharmaceutical or biopharmaceutical industry.
</li>
<li>
Proficient in using a PC and common Microsoft tools such as Word and Excel.
</li>
<li>
Experience with understanding and reviewing electronic data from instrument software.
</li>
<li>
Knowledge of Good Manufacturing Practices (GMP) and documentation rules is an asset.
</li>
<li>
Ability to work a shift-based schedule is required for the 24/7 shift position.
</li>
<li>
Ability to work standard daytime hours is required for the daytime position.
</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>

Why Alvotech
We at Alvotech 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.


Við leitum að tveimur sérfræðingum (Scientist) til að ganga til liðs við Quality Control Product Testing teymið hjá Alvotech. Þessar stöður gegna lykilhlutverki í gæðaeftirliti og losun afurða sem framleiddar eru hjá Alvotech. Stöðurnar eru innan Analytical starfseiningarinnar og styðja við framleiðslu með háþróuðum greiningaraprófunum og gæðaskjölun.

(English below)

We are looking for two Scientists to join the Quality Control Product Testing team at Alvotech. These positions play a vital role in ensuring the quality control and release of products manufactured at Alvotech. The roles are within the Analytical function, supporting manufacturing operations through advanced analytical testing and quality documentation.



The two Scientist positions available are:


 - 

Scientist – Shift Work (24/7 operations)


 - 

Scientist – Daytime Work



Both roles involve similar responsibilities, with work schedules adapted to either a shift‑based or standard daytime working pattern.

Scope and responsibilities:


 - 

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


 - 

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


 - 

Contribute to documentation reviews and updates within the Quality Management System.


 - 

Support investigations related to quality issues, including Invalid assay, OOS/OOT/OOE results.


 - 

Support change controls, CAPAs, and document change controls.


 - 

Perform both routine tasks within established procedures and non-routine tasks such as investigation support, document updates, and CAPAs.


 - 

Carry out routine cleaning, verification, stock checks, and general upkeep of laboratory areas and equipment.


 - 

Perform activities required to support testing, e.g. buffer preparation.





Job requirements:


 - 

Bachelor’s or Master’s degree in a relevant scientific discipline.


 - 

1–5 years of relevant experience in the pharmaceutical or biopharmaceutical industry.


 - 

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


 - 

Experience with understanding and reviewing electronic data from instrument software.


 - 

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


 - 

Ability to work a shift-based schedule is required for the 24/7 shift position.


 - 

Ability to work standard daytime hours is required for the daytime position.





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.





Why Alvotech

We at Alvotech 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.

QC Scientists – Analytical (Shift & Daytime Roles)

Vi&eth; leitum a&eth; &aacute;hugas&ouml;mum einstaklingi til a&eth; ganga til li&eth;s vi&eth; Visual Inspection teymi&eth; okkar &iacute; framlei&eth;slunni. Starfi&eth; felst &iacute; sj&oacute;nr&aelig;nni g&aelig;&eth;asko&eth;un &aacute; fullb&uacute;nu l&iacute;ft&aelig;knilyfi &iacute; reglubundnu umhverfi. Um er a&eth; r&aelig;&eth;a vaktavinnu. &AElig;skilegt er a&eth; ums&aelig;kjandi s&eacute; n&aacute;kv&aelig;mur og me&eth; gott auga fyrir sm&aacute;atri&eth;um. 
[English] 
We are seeking a Technologist to join our Visual Inspection team, responsible for performing visual inspection of pharmaceutical products in a controlled, non-classified (CNC) environment. This is a shift‑based position, requiring flexibility and availability for assigned shifts. The ideal candidate shows strong attention to detail, patience, and strict adherence to procedures, including cGMP and EHS requirements. 
Key Responsibilities
<ul>
<li>
Perform visual inspection of final pharmaceutical products in&nbsp;controlled/non-classified&nbsp;areas (CNC) in accordance with approved procedures
</li>
<li>
Package final products post-inspection in compliance with established procedures
</li>
<li>
Role may require lifting and handling heavy boxes
</li>
<li>
Use computer systems and software to document inspection activities accurately and in compliance with cGMP and data integrity requirements.
</li>
<li>
Support in GMP production activities, including technical and validation support when required
</li>
<li>
Conduct all activities in full compliance with cGMP, EHS, and company quality systems
</li>
<li>
Adhere strictly to SOPs, work instructions, and job-specific procedures
</li>
<li>
Support and contribute, as required, to audits, inspections, and regulatory interactions, including Pre-Approval Inspections (PAIs)
</li>
<li>
Work performed in a dark room designed for visual inspection 
</li>
</ul>
Qualifications
<ul>
<li>
Strong attention to detail, high concentration, and the ability to perform repetitive tasks accurately.
</li>
<li>
Solid understanding of written procedures and commitment to following cGMP, EHS, SOPs, and quality standards.
</li>
<li>
Proficiency in using computers and standard software tools for documentation and daily operations.
</li>
<li>
Team-oriented mindset with the ability to follow guidance and work collaboratively.
</li>
<li>
Basic technical or administrative knowledge relevant to manufacturing environments.
</li>
<li>
Basic knowledge of GMP manufacturing operations; 1&ndash;2 years of experience in technical or production roles is an advantage.
</li>
<li>
Passing a vision test with good eyesight (with or without corrective lenses) is a mandatory&nbsp;for this position.
</li>
</ul>
Successful candidates must demonstrate visual capability suitable for manual visual inspection. This position is critical to product quality and patient safety and requires consistent performance and procedural discipline. 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
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.


Við leitum að áhugasömum einstaklingi til að ganga til liðs við Visual Inspection teymið okkar í framleiðslunni. Starfið felst í sjónrænni gæðaskoðun á fullbúnu líftæknilyfi í reglubundnu umhverfi. Um er að ræða vaktavinnu. Æskilegt er að umsækjandi sé nákvæmur og með gott auga fyrir smáatriðum.



[English]



We are seeking a Technologist to join our Visual Inspection team, responsible for performing visual inspection of pharmaceutical products in a controlled, non-classified (CNC) environment. This is a shift‑based position, requiring flexibility and availability for assigned shifts. The ideal candidate shows strong attention to detail, patience, and strict adherence to procedures, including cGMP and EHS requirements.



Key Responsibilities


 - 

Perform visual inspection of final pharmaceutical products in
controlled/non-classified
areas (CNC) in accordance with approved procedures


 - 

Package final products post-inspection in compliance with established procedures


 - 

Role may require lifting and handling heavy boxes


 - 

Use computer systems and software to document inspection activities accurately and in compliance with cGMP and data integrity requirements.


 - 

Support in GMP production activities, including technical and validation support when required


 - 

Conduct all activities in full compliance with cGMP, EHS, and company quality systems


 - 

Adhere strictly to SOPs, work instructions, and job-specific procedures


 - 

Support and contribute, as required, to audits, inspections, and regulatory interactions, including Pre-Approval Inspections (PAIs)


 - 

Work performed in a dark room designed for visual inspection





Qualifications


 - 

Strong attention to detail, high concentration, and the ability to perform repetitive tasks accurately.


 - 

Solid understanding of written procedures and commitment to following cGMP, EHS, SOPs, and quality standards.


 - 

Proficiency in using computers and standard software tools for documentation and daily operations.


 - 

Team-oriented mindset with the ability to follow guidance and work collaboratively.


 - 

Basic technical or administrative knowledge relevant to manufacturing environments.


 - 

Basic knowledge of GMP manufacturing operations; 1–2 years of experience in technical or production roles is an advantage.


 - 

Passing a vision test with good eyesight (with or without corrective lenses) is a mandatory
for this position.



Successful candidates must demonstrate visual capability suitable for manual visual inspection. This position is critical to product quality and patient safety and requires consistent performance and procedural discipline.

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.



Sérfræðingur í sjónrænni gæðaskoðun / DPVI Technologist

Alvotech leitar a&eth; metna&eth;arfullum s&eacute;rfr&aelig;&eth;ingi til a&eth; ganga til li&eth;s vi&eth; teymi&eth; okkar. &Iacute; &thorn;essu hlutverki munt &thorn;&uacute; sty&eth;ja vi&eth; starfsemi &iacute; framlei&eth;slu l&iacute;ft&aelig;knilyfja, tryggja a&eth; fari&eth; s&eacute; eftir cGMP‑st&ouml;&eth;lum og leggja &thorn;itt af m&ouml;rkum til st&ouml;&eth;ugra umb&oacute;ta &iacute; framlei&eth;sluumhverfinu. Vi&eth; leitum a&eth; lausnami&eth;u&eth;um einstaklingi sem n&yacute;tur &thorn;ess a&eth; starfa &iacute; fj&ouml;lbreyttu og krefjandi vinnuumhverfi og hefur &aacute;huga &aacute; a&eth; vi&eth;halda h&aacute;marks g&aelig;&eth;um og reglufylgni. [English] Alvotech is seeking a dedicated and detail‑oriented Control Operations Specialist to join our team. In this role, you will support key quality operations within biomanufacturing, ensure adherence to cGMP standards, and contribute to continuous improvement across our production environment. We are looking for someone who thrives in a dynamic setting, enjoys problem‑solving, and is committed to maintaining the highest standards of quality and compliance. 
Key Responsibilities
<ul>
<li>
Initiating deviation and performing investigations for deviation reported in Manufacturing.
</li>
<li>
Assisting in creating and reviewing documents such as Standard Operating.
</li>
<li>
Owning Deviations Handling (Non-process, system/facility, and utility related), CAPAs, change controls and Change actions.
</li>
<li>
Trending DEVs in MFG and identifying the Areas for improvement.
</li>
<li>
Develop and maintain metrics to track batch records and deviation turnaround time and assess areas of improvement.
</li>
<li>
Review facility-related risk assessment, EMI deviations and EM trend reports.
</li>
<li>
Providing compliance oversight during biomanufacturing runs including Oversee cGMP activities within DPM production areas (Grade A, B, C and CNC).
</li>
<li>
Troubleshooting and review and approval of quality documents such as planned changes.
</li>
<li>
Tracking and support on-time closure of Quality Records and maintaining compliance against KPIs for the below Quality Records.
</li>
<li>
Effectiveness checks applied for Quality Records.
</li>
<li>
Performing monthly EHS inspection on the production floor.
</li>
<li>
Supporting the review of process logbooks and other GMP records in Manufacturing.
</li>
<li>
Conducting routine facility walkthrough and ensuring that the manufacturing area is maintained in a state of compliance and inspection readiness.
</li>
<li>
Contribute as required to regular audits, and interactions with regulatory agencies.
</li>
</ul>
Qualifications
<ul>
<li>
Degree/Diploma in related discipline or sufficient relevant experience.
</li>
<li>
Knowledge in DP operations is additional benefit to this role.
</li>
<li>
Knowledge of regulatory guidelines for biomanufacturing (FDA, ICH, PIC/s) and implementation.
</li>
<li>
Minimum 3 years in compliance role for biomanufacturing, desired.
</li>
<li>
Experience in supporting Pre-Approval Inspections (PAI) and working with international regulatory agencies including the FDA and EMA.
</li>
<li>
Expertise working with up-to-date cGMP compliance and associated documentation.
</li>
</ul>
What we offer:&nbsp;
<ul>
<li>
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.&nbsp;
</li>
<li>
The chance to be a part of a global and fast-growing company.&nbsp;
</li>
<li>
An international work culture that encourages diversity, collaboration and inclusion.&nbsp;
</li>
<li>
Positive, flexible, and innovative work environment.&nbsp;
</li>
<li>
Support for personal growth and internal career development.&nbsp;
</li>
<li>
Company social events and milestone celebrations.&nbsp;
</li>
<li>
Excellent in-house canteen and coffee house.&nbsp;
</li>
<li>
Exercise and wellbeing support for full-time employees.&nbsp;
</li>
<li>
On-site shower facility.&nbsp;
</li>
<li>
Transportation grant towards eco-friendly modes of travel for full-time employees.&nbsp;
</li>
<li>
Internet at home for full-time employees.
</li>
</ul>
Why Alvotech 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. 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.


Alvotech leitar að metnaðarfullum sérfræðingi til að ganga til liðs við teymið okkar. Í þessu hlutverki munt þú styðja við starfsemi í framleiðslu líftæknilyfja, tryggja að farið sé eftir cGMP‑stöðlum og leggja þitt af mörkum til stöðugra umbóta í framleiðsluumhverfinu. Við leitum að lausnamiðuðum einstaklingi sem nýtur þess að starfa í fjölbreyttu og krefjandi vinnuumhverfi og hefur áhuga á að viðhalda hámarks gæðum og reglufylgni. 

[English] 

Alvotech is seeking a dedicated and detail‑oriented Control Operations Specialist to join our team. In this role, you will support key quality operations within biomanufacturing, ensure adherence to cGMP standards, and contribute to continuous improvement across our production environment. We are looking for someone who thrives in a dynamic setting, enjoys problem‑solving, and is committed to maintaining the highest standards of quality and compliance. 



Key Responsibilities


 - 

Initiating deviation and performing investigations for deviation reported in Manufacturing.


 - 

Assisting in creating and reviewing documents such as Standard Operating.


 - 

Owning Deviations Handling (Non-process, system/facility, and utility related), CAPAs, change controls and Change actions.


 - 

Trending DEVs in MFG and identifying the Areas for improvement.


 - 

Develop and maintain metrics to track batch records and deviation turnaround time and assess areas of improvement.


 - 

Review facility-related risk assessment, EMI deviations and EM trend reports.


 - 

Providing compliance oversight during biomanufacturing runs including Oversee cGMP activities within DPM production areas (Grade A, B, C and CNC).


 - 

Troubleshooting and review and approval of quality documents such as planned changes.


 - 

Tracking and support on-time closure of Quality Records and maintaining compliance against KPIs for the below Quality Records.


 - 

Effectiveness checks applied for Quality Records.


 - 

Performing monthly EHS inspection on the production floor.


 - 

Supporting the review of process logbooks and other GMP records in Manufacturing.


 - 

Conducting routine facility walkthrough and ensuring that the manufacturing area is maintained in a state of compliance and inspection readiness.


 - 

Contribute as required to regular audits, and interactions with regulatory agencies.



Qualifications


 - 

Degree/Diploma in related discipline or sufficient relevant experience.


 - 

Knowledge in DP operations is additional benefit to this role.


 - 

Knowledge of regulatory guidelines for biomanufacturing (FDA, ICH, PIC/s) and implementation.


 - 

Minimum 3 years in compliance role for biomanufacturing, desired.


 - 

Experience in supporting Pre-Approval Inspections (PAI) and working with international regulatory agencies including the FDA and EMA.


 - 

Expertise working with up-to-date cGMP compliance and associated documentation.



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. 

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.

Specialist Tech OPS Control Operations

Latest jobs

Visual Quality Inspection Specialist / DPVI Technologist

&THORN;essi sta&eth;a hentar vel fyrir BSc/MSc &uacute;tskriftarnema sem vilja starfa &iacute; &ouml;flugu teymi sem sty&eth;ur vi&eth; &thorn;r&oacute;un l&iacute;ft&aelig;knilyfja. Engin fyrri reynsla &uacute;r lyfjai&eth;na&eth;i er nau&eth;synleg - full &thorn;j&aacute;lfun og lei&eth;s&ouml;gn er veitt. Vi&eth; leitum a&eth; einstaklingum sem hafa &aacute;huga &aacute; v&iacute;sindum, l&aelig;rd&oacute;msvilja og drifkraft til a&eth; hafa j&aacute;kv&aelig;&eth; &aacute;hrif &aacute; l&iacute;f sj&uacute;klinga.

(English)

This position is well suited for BSc/MSc graduates who want to join a dynamic team responsible for delivering critical materials that support process design for biosimilar medicines. Prior industry experience is not required - full training and mentorship will be provided. We welcome candidates with a strong interest in science, a willingness to learn, and the drive to contribute to improving patients&rsquo; lives.

Regular activities include culturing cells and ensuring batches meet predefined parameters (USP) for cell proliferation. After cell culture and monoclonal antibody (mAb) production, the material is harvested by filtration and processed through a downstream purification process (DSP), which involves chromatography and buffer‑exchange steps before final formulation of the drug product. All activities are documented in a scientific, traceable manner, and the team regularly interprets a wide range of analytical data to understand and improve process performance while ensuring suitability for manufacturing.
&nbsp;
Job Responsibilities
<ul>
<li>
Execute Pilot experiments and batches (cell culture, harvest, purification) efficiently and accurately to support Development activities.
</li>
<li>
Occasionally work to GLP standards to produce bioburden‑free material for toxicology studies.
</li>
<li>
Ensure all data capture is accurate, complete, and compliant with Good Documentation Practices (GDP).
</li>
<li>
Thoroughly document laboratory activities, including writing clear experimental plans and reports.
</li>
<li>
Maintain the work area and equipment in an orderly and compliant manner.
</li>
<li>
Participate in a rotating weekend work schedule as required.
</li>
</ul>

Qualifications
<ul>
<li>
Bachelor&rsquo;s or Master&rsquo;s degree in Life Sciences, Biotechnology, Pharmacy, or a related field.
</li>
<li>
Experience in biotechnology or biopharmaceuticals is an advantage, but not required.
</li>
<li>
Strong collaboration and teamwork skills, with the ability to work effectively with colleagues across functions.
</li>
<li>
Good communication skills and a proactive, solution‑oriented mindset.
</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>
</ul>
<ul>
<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
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.


Þessi staða hentar vel fyrir BSc/MSc útskriftarnema sem vilja starfa í öflugu teymi sem styður við þróun líftæknilyfja. Engin fyrri reynsla úr lyfjaiðnaði er nauðsynleg - full þjálfun og leiðsögn er veitt. Við leitum að einstaklingum sem hafa áhuga á vísindum, lærdómsvilja og drifkraft til að hafa jákvæð áhrif á líf sjúklinga.



(English)



This position is well suited for BSc/MSc graduates who want to join a dynamic team responsible for delivering critical materials that support process design for biosimilar medicines. Prior industry experience is not required - full training and mentorship will be provided. We welcome candidates with a strong interest in science, a willingness to learn, and the drive to contribute to improving patients’ lives.



Regular activities include culturing cells and ensuring batches meet predefined parameters (USP) for cell proliferation. After cell culture and monoclonal antibody (mAb) production, the material is harvested by filtration and processed through a downstream purification process (DSP), which involves chromatography and buffer‑exchange steps before final formulation of the drug product. All activities are documented in a scientific, traceable manner, and the team regularly interprets a wide range of analytical data to understand and improve process performance while ensuring suitability for manufacturing.




Job Responsibilities


 - 

Execute Pilot experiments and batches (cell culture, harvest, purification) efficiently and accurately to support Development activities.


 - 

Occasionally work to GLP standards to produce bioburden‑free material for toxicology studies.


 - 

Ensure all data capture is accurate, complete, and compliant with Good Documentation Practices (GDP).


 - 

Thoroughly document laboratory activities, including writing clear experimental plans and reports.


 - 

Maintain the work area and equipment in an orderly and compliant manner.


 - 

Participate in a rotating weekend work schedule as required.





Qualifications


 - 

Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Pharmacy, or a related field.


 - 

Experience in biotechnology or biopharmaceuticals is an advantage, but not required.


 - 

Strong collaboration and teamwork skills, with the ability to work effectively with colleagues across functions.


 - 

Good communication skills and a proactive, solution‑oriented mindset.





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.

Exciting opportunity at Alvotech / Pilot Scientist

Langar &thorn;ig a&eth; byggja upp feril &iacute; stj&oacute;rnun, pr&oacute;fun og sta&eth;festingu &aacute; GMP‑b&uacute;na&eth;i og kerfum? Hefur &thorn;&uacute; &aacute;huga &aacute; hagn&yacute;tri t&aelig;kni&shy;vinnu sem skiptir raunverulegu m&aacute;li &iacute; framlei&eth;slu &aacute; l&iacute;ft&aelig;knilyfjum?&nbsp;Vi&eth; hj&aacute; Alvotech leitum a&eth; Specialist &iacute; Commissioning &amp; Qualification (C&amp;Q) til a&eth; styrkja teymi&eth; okkar og tryggja a&eth; b&uacute;na&eth;ur, kerfi og a&eth;sta&eth;a uppfylli al&thorn;j&oacute;&eth;lega GMP‑sta&eth;la.
[English]
Are you motivated to grow your career in the management, commissioning, and qualification of GMP pharmaceutical equipment and systems? Do you enjoy hands‑on technical work that contributes directly to high‑quality biopharmaceutical production?&nbsp;We are seeking a Specialist in Commissioning &amp; Qualification (C&amp;Q) to support our team in ensuring that our facilities, systems, and equipment meet global regulatory standards.
In this role, you will assist with commissioning and qualification activities for GMP‑critical systems, collaborating closely with experienced colleagues while developing your skills and technical expertise. You will collaborate across departments, learn industry best practices, and help maintain compliance within a fast‑paced and innovative environment.

Key Responsibilities&nbsp;
<ul>
<li>
Drive and support GMP commissioning and qualification activities for facilities, utilities, and equipment (manufacturing and laboratory).&nbsp;
</li>
<li>
Generate, execute, review, and approve qualification documentation (e.g., URS, IQ/OQ/PQ protocols, validation plans, summary reports).&nbsp;
</li>
<li>
Participate in change control, deviations, and CAPA processes.&nbsp;
</li>
<li>
Collaborate with cross-functional teams including QA, Engineering, Automation, and Project Management.&nbsp;
</li>
<li>
Learn and stay current with industry standards and regulatory requirements.&nbsp;
</li>
<li>
Participate in training and develop competence in qualification and compliance processes.
</li>
</ul>

Qualifications:&nbsp;
<ul>
<li>
Technical degree (Bachelor&rsquo;s or similar) in Engineering, Life Sciences, or another relevant technical field.
</li>
<li>
Basic understanding of GMP principles or a strong willingness to learn.
</li>
<li>
Internship or practical experience in a regulated or technical environment is a plus.
</li>
</ul>

Skills:&nbsp;
<ul>
<li>
Strong analytical and problem-solving mindset.&nbsp;
</li>
<li>
Clear and effective communication skills.
</li>
<li>
Organised, dependable, and eager to learn.
</li>
<li>
Ability to manage tasks with support and guidance.
</li>
<li>
Collaborative approach and willingness to work cross‑functionally.
</li>
</ul>

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


Langar þig að byggja upp feril í stjórnun, prófun og staðfestingu á GMP‑búnaði og kerfum? Hefur þú áhuga á hagnýtri tækni­vinnu sem skiptir raunverulegu máli í framleiðslu á líftæknilyfjum?
Við hjá Alvotech leitum að Specialist í Commissioning &amp; Qualification (C&amp;Q) til að styrkja teymið okkar og tryggja að búnaður, kerfi og aðstaða uppfylli alþjóðlega GMP‑staðla.

[English]

Are you motivated to grow your career in the management, commissioning, and qualification of GMP pharmaceutical equipment and systems? Do you enjoy hands‑on technical work that contributes directly to high‑quality biopharmaceutical production?
We are seeking a Specialist in Commissioning &amp; Qualification (C&amp;Q) to support our team in ensuring that our facilities, systems, and equipment meet global regulatory standards.

In this role, you will assist with commissioning and qualification activities for GMP‑critical systems, collaborating closely with experienced colleagues while developing your skills and technical expertise. You will collaborate across departments, learn industry best practices, and help maintain compliance within a fast‑paced and innovative environment.



Key Responsibilities



 - 

Drive and support GMP commissioning and qualification activities for facilities, utilities, and equipment (manufacturing and laboratory).



 - 

Generate, execute, review, and approve qualification documentation (e.g., URS, IQ/OQ/PQ protocols, validation plans, summary reports).



 - 

Participate in change control, deviations, and CAPA processes.



 - 

Collaborate with cross-functional teams including QA, Engineering, Automation, and Project Management.



 - 

Learn and stay current with industry standards and regulatory requirements.



 - 

Participate in training and develop competence in qualification and compliance processes.





Qualifications:



 - 

Technical degree (Bachelor’s or similar) in Engineering, Life Sciences, or another relevant technical field.


 - 

Basic understanding of GMP principles or a strong willingness to learn.


 - 

Internship or practical experience in a regulated or technical environment is a plus.





Skills:



 - 

Strong analytical and problem-solving mindset.



 - 

Clear and effective communication skills.


 - 

Organised, dependable, and eager to learn.


 - 

Ability to manage tasks with support and guidance.


 - 

Collaborative approach and willingness to work cross‑functionally.





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.
