Alvotech er fjölþjóðlegt hátæknifyrirtæki í fremstu röð, þar sem yfir 1000 starfsmenn af um 64 þjóðernum vinna að því að móta framtíðina á sviði líftæknilyfja og auka aðgengi sjúklinga um allan heim að hágæða lyfjum. Margir af færustu vísindamönnum landsins starfa hjá fyrirtækinu. 

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 allra starfsmanna, hérlendis jafnt sem erlendis. Við viljum laða að okkur færasta fólkið á hverju sviði, án tillits til uppruna eða kyns. Með þessum hætti getum við best þjónað hagsmunum sjúklinga og samstarfsaðilum okkar. 

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


1001-5000

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

Jafnlaunavottun

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Робоче середовище

Alvotech leitar a&eth; einstaklingi til a&eth; ganga til li&eth;s vi&eth; flutningateymi&eth; sem S&eacute;rfr&aelig;&eth;ingur &iacute; flutningum. Alvotech starfar &iacute; mj&ouml;g reglubundnu umhverfi og vi&eth; leitum a&eth; einstaklingi sem hefur j&aacute;kv&aelig;tt vi&eth;horf, tekur &aacute;skorunum og err sveigjanlegur.

Helstu verkefni:
<ul>
<li>St&yacute;ra daglegum samskiptum vi&eth; flutningafyrirt&aelig;ki.</li>
<li>Fylgja sendingum &aacute; me&eth;an &aacute; flutningi stendur og tryggja a&eth; sendingar berist &aacute; &aacute;fangasta&eth; &aacute; r&eacute;ttum t&iacute;ma.</li>
<li>Samskipti vi&eth; v&ouml;ruh&uacute;s Alvotech &iacute; Evr&oacute;pu.</li>
<li>Tryggja a&eth; flutningsskj&ouml;l fyrir hr&aacute;efni og v&ouml;rur s&eacute;u ger&eth; fyrir sendingar &aacute; r&eacute;ttum t&iacute;ma og uppfylli inn- og &uacute;tflutningsl&ouml;ggj&ouml;f.</li>
<li>Skr&aacute; sendingarg&ouml;gn til a&eth; vi&eth;halda m&aelig;likv&ouml;r&eth;um (KPI).</li>
<li>Vinna n&aacute;i&eth; me&eth; me&eth;limum a&eth;fangake&eth;junnar til a&eth; skilgreina flutningskr&ouml;fur og h&aacute;marka skilvirkni &iacute; flutningum.</li>
<li>&THORN;&aacute;tttaka &iacute; umb&oacute;taverkefnum og uppsetningu n&yacute;rra ferla.</li>
</ul>
H&aelig;fniskr&ouml;fur:
<ul>
<li>BSc &iacute; vi&eth;eigandi svi&eth;i er &aelig;skilegt.</li>
<li>Starfsreynsla &iacute; al&thorn;j&oacute;&eth;legum flutningum er kostur.</li>
<li>Reynsla &iacute; lyfjai&eth;na&eth;i er kostur.</li>
<li>H&aelig;fni til a&eth; vinna sj&aacute;lfst&aelig;tt og byggja upp tengsl.</li>
<li>H&aelig;fni til a&eth; eiga &aacute;rangursr&iacute;k samskipti vi&eth; flutningafyrirt&aelig;ki og a&eth;ra tengda a&eth;ila.</li>
<li>Sterk h&aelig;fni &iacute; tengslask&ouml;pun og innri samskiptum, geta til a&eth; eiga frumkv&aelig;&eth;i a&eth; samskiptum vi&eth; a&eth;ila innanh&uacute;s me&eth;an unni&eth; er a&eth; daglegum verkefnum.</li>
<li>H&aelig;fni til a&eth; breg&eth;ast vi&eth; &thorn;j&oacute;nustubei&eth;num &aacute; faglegum h&aacute;tt.</li>
<li>H&aelig;fni til a&eth; b&aelig;ta n&uacute;verandi starfsh&aelig;tti og &aacute;kvar&eth;a skilvirkari ferla til framt&iacute;&eth;ar.</li>
</ul>

[English]

Overview of Role
Alvotech is looking for individuals to join the Logistics team as a Logistics specialist. Alvotech operates in a highly regulated environment and we are looking for individuals that have a positive attitude, embrace challenges, and are flexible and adaptive.

Key Responsibilities:
<ul>
<li>Manage daily communications with logistic carriers and freight forwarders. Monitor shipments during transit and ensure shipments are delivered to the destination in a timely manner.</li>
<li>Communications Alvotech external warehouses in Europe regarding incoming products and release, warehouse capacity planning and overview.</li>
<li>Properly and accurately complete all required paperwork to ensure material and products are ready to ship in a timely manner and conform to corporate policies and comply with import/export laws.</li>
<li>Record shipping data to maintain logistics KPI&rsquo;s and report them</li>
<li>Works closely with end users and Supply Chain members to define shipping requirements and optimizing shipping routes to ensure seamless transportation of goods.</li>
<li>Participation in improvement projects, transport validation studies and setting up new processes.</li>
</ul>

Qualifications:
<ul>
<li>BSc in relevant field is preferred.</li>
<li>Work experience in international logistics and shipping is a plus</li>
<li>Pharma experience is a plus</li>
<li>Ability to work independently and build relationships with stakeholders.</li>
<li>Ability to effectively communicate with logistic carriers and freight forwarders.</li>
<li>Strong relationship building and internal communication skills able to proactively communicate with internal departments while working through daily activities.</li>
<li>Ability to respond to service requests in a timely and professional manner.</li>
<li>Ability to review our processes and expand on current practices, determining more efficient processes moving into the future and implementing best practices preferred</li>
</ul>

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

Why Alvotech

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

Alvotech hf


Alvotech leitar að einstaklingi til að ganga til liðs við flutningateymið sem Sérfræðingur í flutningum. Alvotech starfar í mjög reglubundnu umhverfi og við leitum að einstaklingi sem hefur jákvætt viðhorf, tekur áskorunum og err sveigjanlegur.



Helstu verkefni:


 - Stýra daglegum samskiptum við flutningafyrirtæki.

 - Fylgja sendingum á meðan á flutningi stendur og tryggja að sendingar berist á áfangastað á réttum tíma.

 - Samskipti við vöruhús Alvotech í Evrópu.

 - Tryggja að flutningsskjöl fyrir hráefni og vörur séu gerð fyrir sendingar á réttum tíma og uppfylli inn- og útflutningslöggjöf.

 - Skrá sendingargögn til að viðhalda mælikvörðum (KPI).

 - Vinna náið með meðlimum aðfangakeðjunnar til að skilgreina flutningskröfur og hámarka skilvirkni í flutningum.

 - Þátttaka í umbótaverkefnum og uppsetningu nýrra ferla.


Hæfniskröfur:


 - BSc í viðeigandi sviði er æskilegt.

 - Starfsreynsla í alþjóðlegum flutningum er kostur.

 - Reynsla í lyfjaiðnaði er kostur.

 - Hæfni til að vinna sjálfstætt og byggja upp tengsl.

 - Hæfni til að eiga árangursrík samskipti við flutningafyrirtæki og aðra tengda aðila.

 - Sterk hæfni í tengslasköpun og innri samskiptum, geta til að eiga frumkvæði að samskiptum við aðila innanhús meðan unnið er að daglegum verkefnum.

 - Hæfni til að bregðast við þjónustubeiðnum á faglegum hátt.

 - Hæfni til að bæta núverandi starfshætti og ákvarða skilvirkari ferla til framtíðar.




[English]



Overview of Role

Alvotech is looking for individuals to join the Logistics team as a Logistics specialist. Alvotech operates in a highly regulated environment and we are looking for individuals that have a positive attitude, embrace challenges, and are flexible and adaptive.



Key Responsibilities:


 - Manage daily communications with logistic carriers and freight forwarders. Monitor shipments during transit and ensure shipments are delivered to the destination in a timely manner.

 - Communications Alvotech external warehouses in Europe regarding incoming products and release, warehouse capacity planning and overview.

 - Properly and accurately complete all required paperwork to ensure material and products are ready to ship in a timely manner and conform to corporate policies and comply with import/export laws.

 - Record shipping data to maintain logistics KPI’s and report them

 - Works closely with end users and Supply Chain members to define shipping requirements and optimizing shipping routes to ensure seamless transportation of goods.

 - Participation in improvement projects, transport validation studies and setting up new processes.




Qualifications:


 - BSc in relevant field is preferred.

 - Work experience in international logistics and shipping is a plus

 - Pharma experience is a plus

 - Ability to work independently and build relationships with stakeholders.

 - Ability to effectively communicate with logistic carriers and freight forwarders.

 - Strong relationship building and internal communication skills able to proactively communicate with internal departments while working through daily activities.

 - Ability to respond to service requests in a timely and professional manner.

 - Ability to review our processes and expand on current practices, determining more efficient processes moving into the future and implementing best practices preferred




What we offer:


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

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

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

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

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

 - Internet at home for full-time employees.




Why Alvotech



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

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

Active

Sérfræðingur í flutningum / Logistics Specialist

Alvotech&nbsp;is seeking a dynamic and experienced&nbsp;Finished Product Lead&nbsp;to join our innovative&nbsp;Combination Products and Devices team. In this role, you will lead the development of finished products, coordinate design control processes, and ensure regulatory compliance. At Alvotech, you will collaborate with dedicated professionals to revolutionize global health by developing cutting-edge pharmaceutical products. This is an extraordinary opportunity to make a significant impact on the future of healthcare.

Key Responsibilities:
<ul>
<li>Lead the development of Alvotech's finished products with a cross-functional team.</li>
<li>Coordinate the design control process with program teams.</li>
<li>Review key documents related to combination product development.</li>
<li>Develop and maintain technical knowledge in the function, assembly, and testing of injection devices.</li>
<li>Stay updated on regulations related to combination drug products.</li>
<li>Contribute to process improvements and SOP drafting.</li>
<li>Coordinate consultations and supplier work as needed.</li>
<li>Support efficient batch utilization planning.</li>
</ul>

Qualifications:
<ul>
<li>Master&rsquo;s Degree in a relevant field with a minimum of 10 years of experience in pharmaceutical product development.</li>
<li>Strong leadership and strategic planning skills.</li>
<li>Comprehensive understanding of departmental operations.</li>
<li>Excellent decision-making and problem-solving abilities, demonstrated through successful project outcomes.</li>
<li>High level of independence and accountability for large projects.</li>
<li>Broad knowledge of the enterprise value chain and market value creation, with a focus on pharmaceutical products.</li>
<li>Experience interfacing with both internal and external stakeholders.</li>
<li>Ambitious and proactive, with a hands-on approach to problem-solving and process improvement.</li>
<li>Strong team player, capable of fostering a collaborative work environment.</li>
<li>Excellent verbal and written English communication skills.</li>
</ul>


We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website. 
We encourage you to visit our Career page (link:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C1203600b68924edbbc5108dce39dd29a%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638635514216949197%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=ZppaZTohYvGV6nMErJd%2Bu4I%2FZ%2B53StVRvXZXohUtTag%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a>) It offers valuable insights into our culture, values, and the innovative work we do.


Alvotech
is seeking a dynamic and experienced
Finished Product Lead
to join our innovative
Combination Products and Devices team. In this role, you will lead the development of finished products, coordinate design control processes, and ensure regulatory compliance. At Alvotech, you will collaborate with dedicated professionals to revolutionize global health by developing cutting-edge pharmaceutical products. This is an extraordinary opportunity to make a significant impact on the future of healthcare.



Key Responsibilities:


 - Lead the development of Alvotech's finished products with a cross-functional team.

 - Coordinate the design control process with program teams.

 - Review key documents related to combination product development.

 - Develop and maintain technical knowledge in the function, assembly, and testing of injection devices.

 - Stay updated on regulations related to combination drug products.

 - Contribute to process improvements and SOP drafting.

 - Coordinate consultations and supplier work as needed.

 - Support efficient batch utilization planning.




Qualifications:


 - Master’s Degree in a relevant field with a minimum of 10 years of experience in pharmaceutical product development.

 - Strong leadership and strategic planning skills.

 - Comprehensive understanding of departmental operations.

 - Excellent decision-making and problem-solving abilities, demonstrated through successful project outcomes.

 - High level of independence and accountability for large projects.

 - Broad knowledge of the enterprise value chain and market value creation, with a focus on pharmaceutical products.

 - Experience interfacing with both internal and external stakeholders.

 - Ambitious and proactive, with a hands-on approach to problem-solving and process improvement.

 - Strong team player, capable of fostering a collaborative work environment.

 - Excellent verbal and written English communication skills.






We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website.



We encourage you to visit our Career page (link:
Join us - Alvotech - Better Access Better Lives) It offers valuable insights into our culture, values, and the innovative work we do.

Finished Product Lead

Alvotech augl&yacute;sir eftir skipul&ouml;g&eth;um, j&aacute;kv&aelig;&eth;um og &aacute;hugas&ouml;mum s&eacute;rfr&aelig;&eth;ingi &iacute; &thorn;r&oacute;unardeild m&aelig;lia&eth;fer&eth;a me&eth; auga fyrir sm&aacute;atri&eth;um. Starfi&eth; sn&yacute;st einkum um fj&ouml;lbreyttar s&yacute;nam&aelig;lingar inni &aacute; tilraunastofu &iacute; tengslum vi&eth; lyfja&thorn;r&oacute;un og &thorn;r&oacute;un og gildingar &aacute; m&aelig;lia&eth;fer&eth;um fyrir g&aelig;&eth;astj&oacute;rnun.
Vi&eth;komandi mun starfa innan teymis sem s&eacute;r m.a. um alls kyns kornam&aelig;lingar (&lt; 100 &micro;m), greiningar &aacute; &thorn;r&iacute;v&iacute;ddarbyggingu pr&oacute;teina (DSC, CD, FT-IR, o.fl.), lekapr&oacute;f (&lt; 20 &micro;m), og kraftm&aelig;lingar.
N&yacute;ir starfsmenn f&aacute; fulla &thorn;j&aacute;lfun &aacute;&eth;ur en &thorn;eir hefja st&ouml;rf.

Helstu verkefni og &aacute;byrg&eth;:
<ul>
<li>&Uacute;tb&uacute;a og m&aelig;la s&yacute;ni &iacute; &thorn;&aacute;gu ranns&oacute;kna og &thorn;r&oacute;unar.</li>
<li>Skrifa sk&yacute;rslur og verkl&yacute;singar fyrir &thorn;r&oacute;un og gildingar m&aelig;lia&eth;fer&eth;a.</li>
<li>&THORN;r&oacute;a og gilda m&aelig;lia&eth;fer&eth;ir.</li>
<li>Halda vinnub&oacute;k og fara yfir tilraunastofug&ouml;gn.</li>
<li>Uppf&aelig;ra skj&ouml;l og sk&yacute;rslur eftir &thorn;&ouml;rfum.</li>
<li>Halda utan um einst&ouml;k t&aelig;ki og tilraunastofub&uacute;na&eth;.</li>
<li>&THORN;j&aacute;lfa anna&eth; starfsf&oacute;lk og deila s&eacute;rh&aelig;f&eth;ri &thorn;ekkingu.</li>
<li>&middot;Veita stu&eth;ning &iacute; samskiptum vi&eth; lyfjayfirv&ouml;ld.</li>
</ul>

Menntunar- og h&aelig;fniskr&ouml;fur:
<ul>
<li>Framhaldsn&aacute;m &iacute; e&eth;lisfr&aelig;&eth;i, efnafr&aelig;&eth;i, lyfjafr&aelig;&eth;i, e&eth;a skyldum f&ouml;gum me&eth; t&ouml;luver&eth;u verklegu n&aacute;mi og reynslu og &thorn;ekkingu af tilraunastofuvinnu.</li>
<li>Samb&aelig;rileg starfsreynsla er mikill kostur en ekki krafa.</li>
<li>Mj&ouml;g g&oacute;&eth; enskukunn&aacute;tta &iacute; ritu&eth;u og t&ouml;lu&eth;u m&aacute;li.</li>
<li>Mj&ouml;g g&oacute;&eth; kunn&aacute;tta &iacute; Microsoft Office.</li>
<li>Forritunar- og t&ouml;lfr&aelig;&eth;ikunn&aacute;tta er &aelig;skileg en ekki krafa.</li>
<li>Reynsla og &thorn;ekking af GxP g&aelig;&eth;ast&ouml;&eth;lum er kostur en ekki krafa.</li>
</ul>

Um deildina:
&THORN;r&oacute;unardeild m&aelig;lia&eth;fer&eth;a tilheyrir svi&eth;i ranns&oacute;kna og &thorn;r&oacute;unar hj&aacute; Alvotech. Helstu verkefni deildarinnar eru a&eth; &thorn;r&oacute;a og gilda m&aelig;lia&eth;fer&eth;ir, greina s&yacute;ni &iacute; &thorn;&aacute;gu ranns&oacute;kna og &thorn;r&oacute;unar, og sty&eth;ja a&eth;rar deildir me&eth; ranns&oacute;kna- og &thorn;r&oacute;unarvinnu, me&eth;al annars &iacute; tengslum vi&eth; samskipti vi&eth; lyfjayfirv&ouml;ld.
_______________
[English]
Alvotech is looking for an organized, positive, and enthusiastic individual with attention to detail to join Alvotech&rsquo;s Analytical R&amp;D Physicochemical Assays department as an Analytical R&amp;D Scientist. The job involves various types of sample testing to support product development and regulatory submissions as well as developing and validating analytical methods to ensure quality biopharmaceutical products.
The candidate will become part of a team that focuses, among other things, on subvisible (&lt; 100 &micro;m) particle analysis, higher order structure determination of proteins (DSC, CD, FT-IR, etc.), container closure integrity testing (&lt; 20 &micro;m) and functional testing.
New employees will receive comprehensive training before starting independent work.
Key Responsibilities:
<ul>
<li>Analyze samples to support research and development.</li>
<li>Write reports and protocols for method development and validation.</li>
<li>Develop and validate analytical methods.</li>
<li>Review and complete laboratory documentation.</li>
<li>Update quality documentation as needed.</li>
<li>Maintain and verify laboratory equipment.</li>
<li>Provide technical training and support.</li>
<li>Assist with regulatory documentation.</li>
</ul>
Qualifications:
<ul>
<li>M.Sc. in physics, chemistry, pharmacy, or a related field with a substantial experimental component.</li>
<li>Relevant professional experience is highly advantageous but not a requirement.</li>
<li>Fluency in English, both written and spoken.</li>
<li>Proficient in Microsoft Office.</li>
<li>Programming and statistical analysis skills are beneficial but not required.</li>
<li>Knowledge of current GxP standards is beneficial but not required.</li>
</ul>

About the department:
The Analytical R&amp;D Physicochemical Assays department is part of the R&amp;D organization within Alvotech. The main role is to develop and validate analytical methods, analyze samples as part of research and analytical development programs, participate in execution of analytical strategies, and support preparation of all regulatory documentation.
________________________
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>


Alvotech auglýsir eftir skipulögðum, jákvæðum og áhugasömum sérfræðingi í þróunardeild mæliaðferða með auga fyrir smáatriðum. Starfið snýst einkum um fjölbreyttar sýnamælingar inni á tilraunastofu í tengslum við lyfjaþróun og þróun og gildingar á mæliaðferðum fyrir gæðastjórnun.

Viðkomandi mun starfa innan teymis sem sér m.a. um alls kyns kornamælingar (&lt; 100 µm), greiningar á þrívíddarbyggingu próteina (DSC, CD, FT-IR, o.fl.), lekapróf (&lt; 20 µm), og kraftmælingar.

Nýir starfsmenn fá fulla þjálfun áður en þeir hefja störf.



Helstu verkefni og ábyrgð:


 - Útbúa og mæla sýni í þágu rannsókna og þróunar.

 - Skrifa skýrslur og verklýsingar fyrir þróun og gildingar mæliaðferða.

 - Þróa og gilda mæliaðferðir.

 - Halda vinnubók og fara yfir tilraunastofugögn.

 - Uppfæra skjöl og skýrslur eftir þörfum.

 - Halda utan um einstök tæki og tilraunastofubúnað.

 - Þjálfa annað starfsfólk og deila sérhæfðri þekkingu.

 - ·Veita stuðning í samskiptum við lyfjayfirvöld.




Menntunar- og hæfniskröfur:


 - Framhaldsnám í eðlisfræði, efnafræði, lyfjafræði, eða skyldum fögum með töluverðu verklegu námi og reynslu og þekkingu af tilraunastofuvinnu.

 - Sambærileg starfsreynsla er mikill kostur en ekki krafa.

 - Mjög góð enskukunnátta í rituðu og töluðu máli.

 - Mjög góð kunnátta í Microsoft Office.

 - Forritunar- og tölfræðikunnátta er æskileg en ekki krafa.

 - Reynsla og þekking af GxP gæðastöðlum er kostur en ekki krafa.




Um deildina:

Þróunardeild mæliaðferða tilheyrir sviði rannsókna og þróunar hjá Alvotech. Helstu verkefni deildarinnar eru að þróa og gilda mæliaðferðir, greina sýni í þágu rannsókna og þróunar, og styðja aðrar deildir með rannsókna- og þróunarvinnu, meðal annars í tengslum við samskipti við lyfjayfirvöld.

_______________

[English]

Alvotech is looking for an organized, positive, and enthusiastic individual with attention to detail to join Alvotech’s Analytical R&amp;D Physicochemical Assays department as an Analytical R&amp;D Scientist. The job involves various types of sample testing to support product development and regulatory submissions as well as developing and validating analytical methods to ensure quality biopharmaceutical products.

The candidate will become part of a team that focuses, among other things, on subvisible (&lt; 100 µm) particle analysis, higher order structure determination of proteins (DSC, CD, FT-IR, etc.), container closure integrity testing (&lt; 20 µm) and functional testing.

New employees will receive comprehensive training before starting independent work.

Key Responsibilities:


 - Analyze samples to support research and development.

 - Write reports and protocols for method development and validation.

 - Develop and validate analytical methods.

 - Review and complete laboratory documentation.

 - Update quality documentation as needed.

 - Maintain and verify laboratory equipment.

 - Provide technical training and support.

 - Assist with regulatory documentation.


Qualifications:


 - M.Sc. in physics, chemistry, pharmacy, or a related field with a substantial experimental component.

 - Relevant professional experience is highly advantageous but not a requirement.

 - Fluency in English, both written and spoken.

 - Proficient in Microsoft Office.

 - Programming and statistical analysis skills are beneficial but not required.

 - Knowledge of current GxP standards is beneficial but not required.




About the department:

The Analytical R&amp;D Physicochemical Assays department is part of the R&amp;D organization within Alvotech. The main role is to develop and validate analytical methods, analyze samples as part of research and analytical development programs, participate in execution of analytical strategies, and support preparation of all regulatory 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.




Sérfræðingur í þróunardeild mæliaðferða

Alvotech leitar eftir &ouml;flugum a&eth;ila &iacute; hlutverki&eth;&nbsp;Pharmaceutical Sciences Lead,&nbsp;&thorn;ar sem helsta verkefni&eth; er a&eth; hafa yfirs&yacute;n yfir &thorn;r&oacute;unarvinnunni innan PharmSci og vera hvatberi samskipta og samvinnu milli allra deilda sem koma a&eth; verkefninu fr&aacute; upphafi &thorn;ess, til ums&oacute;knar til yfirvalda og sam&thorn;ykkis &aacute; verkefninu fr&aacute; yfirv&ouml;ldum. &Iacute; &thorn;essu lykilhlutverki vinnur a&eth;ilinn me&eth; m&ouml;rgum mismunandi deildum innan &thorn;r&oacute;unarinnar (e. CMC development) (&thorn;.m.t. Process Development, Analytical Development, MSAT, o.s.frv.), &thorn;ar sem sameiginlegt markmi&eth; er a&eth; finna n&yacute;st&aacute;rlega stefnu til &thorn;r&oacute;unar og framkv&aelig;ma &thorn;&aacute; stefnu til a&eth; tryggja framvindu verkefnisins. Hlutverki&eth; gefur t&aelig;kif&aelig;ri til a&eth; vinna me&eth; &ouml;&eth;rum deildum innan Alvotech, &thorn;ar sem a&eth;ilinn mun lei&eth;a &thorn;verfaglegt teymi sem vinnur a&eth; &thorn;r&oacute;uninni &aacute;samt &thorn;v&iacute; a&eth; vera fulltr&uacute;i &thorn;r&oacute;unarteymisins innan annarra teyma sem koma a&eth; verkefninu, til a&eth; tryggja &aacute;rangur verkefnisins (t.d. Clinical, Regulatory, Commercial, o.s.frv.).

Vi&eth; bj&oacute;&eth;um upp &aacute; skemmtilegt og krefjandi starf &iacute; al&thorn;j&oacute;&eth;legu umhverfi &aacute;samt fj&ouml;lbreyttum t&aelig;kif&aelig;rum til starfs&thorn;r&oacute;unar. Ef &thorn;&uacute; hefur &aacute;huga &aacute; &thorn;essu spennandi t&aelig;kif&aelig;ri, hvetjum vi&eth; &thorn;ig til a&eth; kynna &thorn;&eacute;r &thorn;a&eth; betur &aacute; heimas&iacute;&eth;u okkar.

[English]

Overview of role:

Alvotech is looking to hire a dynamic&nbsp;Pharmaceutical Sciences Lead&nbsp;to oversee and coordinate all PharmSci development activities from program inception through submission and approval. In this pivotal role, you'll collaborate with various line functions responsible for the CMC development (e.g. Process Development, Analytical Development, MSAT etc.) to craft innovative PharmSci strategies and drive the execution of the strategies to ensure efficient progression of the CMC activities. Leading the technical development sub-team, you'll also represent the PharmSci function in program team meetings, working closely with different stakeholders across the organization (e.g. Clinical, Regulatory, Commercial etc.) and contribute to the overall advancement of the programs.

Key Responsibilities:

<ul>
<li>Lead the Co-development sub-team and represent the function in cross-functional teams.</li>
<li>Co-ordinate with the relevant stakeholders to design the strategy for CMC development</li>
<li>Drive the CMC activities to ensure timely delivery with high quality.</li>
<li>Communicate PharmSci activities and their impact on program timelines.</li>
<li>Oversee PharmSci data to maintain scientific excellence.</li>
<li>Support due diligence activities.</li>
<li>Foster effective team dynamics and communication.</li>
<li>Lead the authoring of CQA, QTPP, and related documents.</li>
<li>Strategize, author and review regulatory submission documents (IMPD, Briefing book, MAA etc.).</li>
<li>Manage PharmSci risks and challenges.</li>
<li>Support daily operations as needed.</li>
</ul>

Qualifications:

<ul>
<li>M.Sc. degree in a relevant scientific discipline with industry experience.</li>
<li>Over 5 years of international experience in PharmSci R&amp;D, preferably with biosimilars.</li>
<li>Proven leadership in PharmSci functions for biological products.</li>
<li>Strong analytical, problem-solving, and organizational skills.</li>
<li>Excellent written and oral communication skills.</li>
<li>Deep scientific knowledge in process and/or analytics for biological products.</li>
<li>Passion for scientific problem solving.</li>
<li>Exceptional communication skills and ability to motivate team members.</li>
</ul>

We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website. 
We encourage you to visit our Career page (link:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C1203600b68924edbbc5108dce39dd29a%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638635514216949197%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=ZppaZTohYvGV6nMErJd%2Bu4I%2FZ%2B53StVRvXZXohUtTag%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a>) It offers valuable insights into our culture, values, and the innovative work we do.


Alvotech leitar eftir öflugum aðila í hlutverkið
Pharmaceutical Sciences Lead,
þar sem helsta verkefnið er að hafa yfirsýn yfir þróunarvinnunni innan PharmSci og vera hvatberi samskipta og samvinnu milli allra deilda sem koma að verkefninu frá upphafi þess, til umsóknar til yfirvalda og samþykkis á verkefninu frá yfirvöldum. Í þessu lykilhlutverki vinnur aðilinn með mörgum mismunandi deildum innan þróunarinnar (e. CMC development) (þ.m.t. Process Development, Analytical Development, MSAT, o.s.frv.), þar sem sameiginlegt markmið er að finna nýstárlega stefnu til þróunar og framkvæma þá stefnu til að tryggja framvindu verkefnisins. Hlutverkið gefur tækifæri til að vinna með öðrum deildum innan Alvotech, þar sem aðilinn mun leiða þverfaglegt teymi sem vinnur að þróuninni ásamt því að vera fulltrúi þróunarteymisins innan annarra teyma sem koma að verkefninu, til að tryggja árangur verkefnisins (t.d. Clinical, Regulatory, Commercial, o.s.frv.).



Við bjóðum upp á skemmtilegt og krefjandi starf í alþjóðlegu umhverfi ásamt fjölbreyttum tækifærum til starfsþróunar. Ef þú hefur áhuga á þessu spennandi tækifæri, hvetjum við þig til að kynna þér það betur á heimasíðu okkar.



[English]



Overview of role:



Alvotech is looking to hire a dynamic
Pharmaceutical Sciences Lead
to oversee and coordinate all PharmSci development activities from program inception through submission and approval. In this pivotal role, you'll collaborate with various line functions responsible for the CMC development (e.g. Process Development, Analytical Development, MSAT etc.) to craft innovative PharmSci strategies and drive the execution of the strategies to ensure efficient progression of the CMC activities. Leading the technical development sub-team, you'll also represent the PharmSci function in program team meetings, working closely with different stakeholders across the organization (e.g. Clinical, Regulatory, Commercial etc.) and contribute to the overall advancement of the programs.



Key Responsibilities:




 - Lead the Co-development sub-team and represent the function in cross-functional teams.

 - Co-ordinate with the relevant stakeholders to design the strategy for CMC development

 - Drive the CMC activities to ensure timely delivery with high quality.

 - Communicate PharmSci activities and their impact on program timelines.

 - Oversee PharmSci data to maintain scientific excellence.

 - Support due diligence activities.

 - Foster effective team dynamics and communication.

 - Lead the authoring of CQA, QTPP, and related documents.

 - Strategize, author and review regulatory submission documents (IMPD, Briefing book, MAA etc.).

 - Manage PharmSci risks and challenges.

 - Support daily operations as needed.




Qualifications:




 - M.Sc. degree in a relevant scientific discipline with industry experience.

 - Over 5 years of international experience in PharmSci R&amp;D, preferably with biosimilars.

 - Proven leadership in PharmSci functions for biological products.

 - Strong analytical, problem-solving, and organizational skills.

 - Excellent written and oral communication skills.

 - Deep scientific knowledge in process and/or analytics for biological products.

 - Passion for scientific problem solving.

 - Exceptional communication skills and ability to motivate team members.




We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website.



We encourage you to visit our Career page (link:
Join us - Alvotech - Better Access Better Lives) It offers valuable insights into our culture, values, and the innovative work we do.

PharmSci Lead

Останні вакансії

Спеціаліст з логістики

Керівник готової продукції

Спеціаліст відділу розробки методів вимірювання

Керівник фармацевтичного факультету

Alvotech leitar a&eth; v&iacute;sindamanni &iacute; gagnastj&oacute;rnun til a&eth; ganga til li&eth;s vi&eth; PharmSci Strategy &amp; Execution. &THORN;essi sta&eth;a felur &iacute; s&eacute;r a&eth; skipuleggja, samr&aelig;ma og hafa umsj&oacute;n me&eth; gagnastj&oacute;rnun sem tengist kl&iacute;n&iacute;skum birg&eth;um, g&aelig;&eth;alosun, gagnavinnslu og skj&ouml;lum sem uppfylla GMP og GCP sta&eth;la.
Vi&eth; bj&oacute;&eth;um upp &aacute; skemmtilegt og krefjandi starf &iacute; al&thorn;j&oacute;&eth;legu umhverfi &aacute;samt fj&ouml;lbreyttum t&aelig;kif&aelig;rum til starfs&thorn;r&oacute;unar. Ef &thorn;&uacute; hefur &aacute;huga &aacute; &thorn;essu spennandi t&aelig;kif&aelig;ri, hvetjum vi&eth; &thorn;ig til a&eth; kynna &thorn;&eacute;r &thorn;a&eth; betur &aacute; heimas&iacute;&eth;u okkar! 
Vi&eth; hvetjum &thorn;ig einnig til a&eth; sko&eth;a starfas&iacute;&eth;una okkar:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C7ae86df454cf4e35e44d08dcd8068404%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638622769693940279%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=DIfyOPk%2BDLdwhPyg%2FbBK9o5hMo%2FcC0yKMZqPozqlCSQ%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a>&nbsp;sem veitir g&oacute;&eth;a inns&yacute;n &iacute; vinnusta&eth;amenninguna, gildin okkar og &thorn;a&eth; frumkv&ouml;&eth;la starf sem vi&eth; st&ouml;ndum fyrir.
&nbsp; [English] Overview of role: Alvotech is looking for a Senior Scientist in Data Management to join our PharmSci Strategy &amp; Execution department. This role focuses on coordinating, overseeing, and managing data related to clinical supplies, quality release, data processing, and document handling in compliance with GMP and GCP standards.

Key Responsibilities:
<ul>
<li>Coordinate tasks and activities for planning, oversight and release of clinical supplies, with the clinical operations team, the Contract Manufacturing Organisation (CMO) and Contract Research Organisation (CRO).</li>
<li>Act as the key point of contact for review of documents related to clinical supply manufacturing, stability testing and quality release for clinical trials.</li>
<li>Act as key point of contact for temperature excursions and other information containing unblinded treatment allocation information.</li>
<li>Prepare and plan detailed process for all steps and tasks for management of Clinical Supplies until delivery to sites or country depots, including but not limited to, packaging, labelling and blinding activities.</li>
<li>Define process for full QP release.</li>
<li>Develop Investigational Medicinal Product (IMP) distribution and returns drug plans and manage clinical supply documentation to maintain Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) compliance, in accordance to project scope and timelines.</li>
<li>Collaborate with cross-functional individuals (e.g. Clinical Operations, Clinical &amp; Medical Quality, Global Regulatory Affairs, Program Management, Pharmaceutical Science Stability testing, TechOps, Quality Assurance and Qualified Persons).</li>
<li>Review clinical supply packaging and labelling documentation</li>
<li>Co-ordinate review of electronic Batch Records</li>
<li>Act as primary Point of Contact internally and externally (CRO and clinical site as needed) for Temperature Excursion notifications.</li>
<li>Review Temperature Excursion documentation and co-ordinate assessment of Fit-For-Use decision.</li>
</ul>

Qualifications:
<ul>
<li>BSc in a scientific subject, preferably Biotechnology or similar.</li>
<li>Experience in data gathering, summarizing and evaluation.</li>
<li>Good working knowledge with Word and Excel, familiarity with GraphPad Prism or JMP is a plus.</li>
<li>Ability to work independently and cross-functionally with diverse teams.</li>
<li>Strong organizational, multitasking, and adaptability skills.</li>
</ul>

 We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website. 
We encourage you to visit our Career page (link:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C1203600b68924edbbc5108dce39dd29a%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638635514216949197%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=ZppaZTohYvGV6nMErJd%2Bu4I%2FZ%2B53StVRvXZXohUtTag%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a>) It offers valuable insights into our culture, values, and the innovative work we do.


Alvotech leitar að vísindamanni í gagnastjórnun til að ganga til liðs við PharmSci Strategy &amp; Execution. Þessi staða felur í sér að skipuleggja, samræma og hafa umsjón með gagnastjórnun sem tengist klínískum birgðum, gæðalosun, gagnavinnslu og skjölum sem uppfylla GMP og GCP staðla.

Við bjóðum upp á skemmtilegt og krefjandi starf í alþjóðlegu umhverfi ásamt fjölbreyttum tækifærum til starfsþróunar. Ef þú hefur áhuga á þessu spennandi tækifæri, hvetjum við þig til að kynna þér það betur á heimasíðu okkar!


Við hvetjum þig einnig til að skoða starfasíðuna okkar:
Join us - Alvotech - Better Access Better Lives
sem veitir góða innsýn í vinnustaðamenninguna, gildin okkar og það frumkvöðla starf sem við stöndum fyrir.



[English] 

Overview of role: 

Alvotech is looking for a Senior Scientist in Data Management to join our PharmSci Strategy &amp; Execution department. This role focuses on coordinating, overseeing, and managing data related to clinical supplies, quality release, data processing, and document handling in compliance with GMP and GCP standards.



Key Responsibilities:


 - Coordinate tasks and activities for planning, oversight and release of clinical supplies, with the clinical operations team, the Contract Manufacturing Organisation (CMO) and Contract Research Organisation (CRO).

 - Act as the key point of contact for review of documents related to clinical supply manufacturing, stability testing and quality release for clinical trials.

 - Act as key point of contact for temperature excursions and other information containing unblinded treatment allocation information.

 - Prepare and plan detailed process for all steps and tasks for management of Clinical Supplies until delivery to sites or country depots, including but not limited to, packaging, labelling and blinding activities.

 - Define process for full QP release.

 - Develop Investigational Medicinal Product (IMP) distribution and returns drug plans and manage clinical supply documentation to maintain Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) compliance, in accordance to project scope and timelines.

 - Collaborate with cross-functional individuals (e.g. Clinical Operations, Clinical &amp; Medical Quality, Global Regulatory Affairs, Program Management, Pharmaceutical Science Stability testing, TechOps, Quality Assurance and Qualified Persons).

 - Review clinical supply packaging and labelling documentation

 - Co-ordinate review of electronic Batch Records

 - Act as primary Point of Contact internally and externally (CRO and clinical site as needed) for Temperature Excursion notifications.

 - Review Temperature Excursion documentation and co-ordinate assessment of Fit-For-Use decision.




Qualifications:


 - BSc in a scientific subject, preferably Biotechnology or similar.

 - Experience in data gathering, summarizing and evaluation.

 - Good working knowledge with Word and Excel, familiarity with GraphPad Prism or JMP is a plus.

 - Ability to work independently and cross-functionally with diverse teams.

 - Strong organizational, multitasking, and adaptability skills.





We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website.



We encourage you to visit our Career page (link:
Join us - Alvotech - Better Access Better Lives) It offers valuable insights into our culture, values, and the innovative work we do.

Науковець - Управління даними

Alvotech is looking to hire a&nbsp;Senior Principal Scientist&nbsp;to lead and innovate within our&nbsp;clinical pharmacology team. This role offers the opportunity to make a significant impact on our clinical programs and contribute to the development of groundbreaking therapies.
We seek a highly experienced scientist with a deep understanding of clinical pharmacology, PKPD analysis, and population modelling. Your expertise will be crucial in designing and planning clinical trials, developing regulatory documents, and ensuring compliance with global standards.
At Alvotech, you will play a key role in our mission to improve global access to affordable medicines. You will be part of a dynamic team dedicated to scientific excellence and innovation, enjoying a collaborative work environment, opportunities for professional growth, and the chance to contribute to transformative therapies.
Please note that international travel may be required to support departmental activities.

Scope &amp; Responsibilities:
<ul>
<li>Lead clinical pharmacology activities for assigned clinical programs/trials.</li>
<li>Develop and revise relevant sections of regulatory documents and deliverables.</li>
<li>Develop the clinical pharmacology strategy, briefing book, study design, and protocol development. Collaborate with biostatisticians on Statistical Analysis Plans (SAPs) and review mock-up displays for tables, listings, and figures.</li>
<li>Provide statistical consultation to clinical teams and support decision-making processes.</li>
<li>Ensure GCP compliance and high-quality standards for Alvotech's sponsored clinical trials.</li>
<li>Support internal and external resources in assay development and validation.</li>
<li>Work independently and as part of a multifunctional team to achieve project deliverables.</li>
</ul>

Job Requirements:
<ul>
<li>Master's Degree in a related discipline (PhD in Clinical Pharmacology or related discipline with relevant experience is desirable).</li>
<li>Minimum 10 years of experience in clinical trials or clinical pharmacology.</li>
<li>Expertise in PKPD analysis, population modelling, and simulation.</li>
<li>Experience with large molecules and biosimilars is desired.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficiency in technical software such as Phoenix, WinNonlin, SAS, R, Monolix, and NONMEM.</li>
<li>Strong organizational and management skills.</li>
<li>Deep knowledge of ICH-GCP and regulatory guidelines.</li>
<li>Proven ability to collaborate effectively within cross-functional teams.</li>
<li>Strong interpersonal skills, including the ability to build team spirit and communicate openly.</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 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>A clear and developed organizational structure.</li>
<li>Training and global opportunities to advance.</li>
<li>A good work-life balance.</li>
<li>Home internet and home office equipment.</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.


Alvotech is looking to hire a
Senior Principal Scientist
to lead and innovate within our
clinical pharmacology team. This role offers the opportunity to make a significant impact on our clinical programs and contribute to the development of groundbreaking therapies.

We seek a highly experienced scientist with a deep understanding of clinical pharmacology, PKPD analysis, and population modelling. Your expertise will be crucial in designing and planning clinical trials, developing regulatory documents, and ensuring compliance with global standards.

At Alvotech, you will play a key role in our mission to improve global access to affordable medicines. You will be part of a dynamic team dedicated to scientific excellence and innovation, enjoying a collaborative work environment, opportunities for professional growth, and the chance to contribute to transformative therapies.

Please note that international travel may be required to support departmental activities.



Scope &amp; Responsibilities:


 - Lead clinical pharmacology activities for assigned clinical programs/trials.

 - Develop and revise relevant sections of regulatory documents and deliverables.

 - Develop the clinical pharmacology strategy, briefing book, study design, and protocol development. Collaborate with biostatisticians on Statistical Analysis Plans (SAPs) and review mock-up displays for tables, listings, and figures.

 - Provide statistical consultation to clinical teams and support decision-making processes.

 - Ensure GCP compliance and high-quality standards for Alvotech's sponsored clinical trials.

 - Support internal and external resources in assay development and validation.

 - Work independently and as part of a multifunctional team to achieve project deliverables.




Job Requirements:


 - Master's Degree in a related discipline (PhD in Clinical Pharmacology or related discipline with relevant experience is desirable).

 - Minimum 10 years of experience in clinical trials or clinical pharmacology.

 - Expertise in PKPD analysis, population modelling, and simulation.

 - Experience with large molecules and biosimilars is desired.

 - Excellent written and verbal communication skills.

 - Proficiency in technical software such as Phoenix, WinNonlin, SAS, R, Monolix, and NONMEM.

 - Strong organizational and management skills.

 - Deep knowledge of ICH-GCP and regulatory guidelines.

 - Proven ability to collaborate effectively within cross-functional teams.

 - Strong interpersonal skills, including the ability to build team spirit and communicate openly.




What we offer:


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

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

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

 - Positive, flexible, and innovative work environment.

 - A clear and developed organizational structure.

 - Training and global opportunities to advance.

 - A good work-life balance.

 - Home internet and home office equipment.




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.

Старший науковий співробітник – клінічна фармакологія

Hefur &thorn;&uacute; &aacute;huga &aacute; a&eth; st&yacute;ra og hafa umsj&oacute;n me&eth; uppl&yacute;singakerfum? Alvotech leitar a&eth; metna&eth;arfullum og h&aelig;fileikar&iacute;kum IT s&eacute;rfr&aelig;&eth;ingi &iacute; greiningarvinnu til a&eth; ganga t&iacute;mabundi&eth; til li&eth;s vi&eth; uppl&yacute;singat&aelig;kniteymi sitt.

Helstu verkefni og &aacute;byrg&eth;:
<ul>
<li>Reynsla af stj&oacute;rnun og vi&eth;haldi uppl&yacute;singakerfa.</li>
<li>H&aelig;fni til a&eth; sty&eth;ja vi&eth; kerfisuppf&aelig;rslur og &uacute;rb&aelig;tur.</li>
<li>G&oacute;&eth; samskiptah&aelig;fni til a&eth; vinna me&eth; &thorn;j&oacute;nustua&eth;ilum og birgjum.</li>
<li>&THORN;ekking &aacute; n&yacute;justu t&aelig;knistefnum.</li>
<li>S&eacute;rfr&aelig;&eth;i&thorn;ekking &aacute; uppl&yacute;singakerfum.</li>
<li>F&aelig;rni til a&eth; halda verklagsreglum og ferlum uppf&aelig;r&eth;um.</li>
<li>Reynsla af ger&eth; sta&eth;la&eth;ra vinnureglna (SOPs).</li>
<li>H&aelig;fni &iacute; notenda&thorn;j&aacute;lfun og stu&eth;ningi.</li>
<li>Geta til a&eth; a&eth;sto&eth;a vi&eth; kerfispr&oacute;fanir og vottun.</li>
</ul>

H&aelig;fniskr&ouml;fur:
<ul>
<li>H&aacute;sk&oacute;lagr&aacute;&eth;a sem n&yacute;tist &iacute; starfi e&eth;a samb&aelig;rileg starfsreynsla.</li>
<li>A&eth; minnsta kosti 2 &aacute;ra reynsla &iacute; lyfjai&eth;na&eth;i.</li>
<li>&THORN;ekking &aacute; GxP reglum.</li>
<li>Reynsla af me&eth;h&ouml;ndlun t&ouml;lvukerfa.</li>
<li>&THORN;ekking &aacute; ranns&oacute;knarstofukerfum og ferlum.</li>
<li>Fram&uacute;rskarandi skrifleg og munnleg samskiptah&aelig;fni &aacute; ensku.</li>
<li>Sterk greiningarh&aelig;fni.</li>
<li>H&aelig;fni til a&eth; st&yacute;ra m&ouml;rgum verkefnum samt&iacute;mis.</li>
<li>G&oacute;&eth; skipulags- og stj&oacute;rnunarh&aelig;fni.</li>
</ul>

Overview of role:
<ul>
<li>Are you passionate about driving the life cycle management and administration of IT systems? Alvotech is looking for a passionate and skilled IT Specialist in Analytical Applications&nbsp;to temporarily join our Information Technology team.&nbsp;</li>
</ul>

Key Responsibilities:
<ul>
<li>Experience in managing and maintaining IT systems.</li>
<li>Ability to support system upgrades and improvements.</li>
<li>Good communication skills for working with vendors and service providers.</li>
<li>Knowledge of the latest technology trends.</li>
<li>Expertise in IT systems.</li>
<li>Ability to keep processes and procedures up-to-date.</li>
<li>Experience in writing Standard Operating Procedures (SOPs).</li>
<li>Skills in user training and support.</li>
<li>Ability to assist with system testing and qualification.</li>
</ul>

Qualifications:
<ul>
<li>Bachelor's degree or relevant business experience.</li>
<li>At least 2 years of experience in the Pharmaceutical or Medical Device Industry.</li>
<li>Familiarity with GxP regulatory requirements.</li>
<li>Experience in validating computer systems.</li>
<li>Knowledge of laboratory systems and processes.</li>
<li>Excellent written and verbal communication skills in English.</li>
<li>Strong analytical and interpersonal skills.</li>
<li>Ability to manage multiple tasks simultaneously.</li>
<li>Excellent organizational and management skills.</li>
</ul>

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

Why Alvotech
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.


Hefur þú áhuga á að stýra og hafa umsjón með upplýsingakerfum? Alvotech leitar að metnaðarfullum og hæfileikaríkum IT sérfræðingi í greiningarvinnu til að ganga tímabundið til liðs við upplýsingatækniteymi sitt.



Helstu verkefni og ábyrgð:


 - Reynsla af stjórnun og viðhaldi upplýsingakerfa.

 - Hæfni til að styðja við kerfisuppfærslur og úrbætur.

 - Góð samskiptahæfni til að vinna með þjónustuaðilum og birgjum.

 - Þekking á nýjustu tæknistefnum.

 - Sérfræðiþekking á upplýsingakerfum.

 - Færni til að halda verklagsreglum og ferlum uppfærðum.

 - Reynsla af gerð staðlaðra vinnureglna (SOPs).

 - Hæfni í notendaþjálfun og stuðningi.

 - Geta til að aðstoða við kerfisprófanir og vottun.




Hæfniskröfur:


 - Háskólagráða sem nýtist í starfi eða sambærileg starfsreynsla.

 - Að minnsta kosti 2 ára reynsla í lyfjaiðnaði.

 - Þekking á GxP reglum.

 - Reynsla af meðhöndlun tölvukerfa.

 - Þekking á rannsóknarstofukerfum og ferlum.

 - Framúrskarandi skrifleg og munnleg samskiptahæfni á ensku.

 - Sterk greiningarhæfni.

 - Hæfni til að stýra mörgum verkefnum samtímis.

 - Góð skipulags- og stjórnunarhæfni.




Overview of role:


 - Are you passionate about driving the life cycle management and administration of IT systems? Alvotech is looking for a passionate and skilled IT Specialist in Analytical Applications
to temporarily join our Information Technology team.





Key Responsibilities:


 - Experience in managing and maintaining IT systems.

 - Ability to support system upgrades and improvements.

 - Good communication skills for working with vendors and service providers.

 - Knowledge of the latest technology trends.

 - Expertise in IT systems.

 - Ability to keep processes and procedures up-to-date.

 - Experience in writing Standard Operating Procedures (SOPs).

 - Skills in user training and support.

 - Ability to assist with system testing and qualification.




Qualifications:


 - Bachelor's degree or relevant business experience.

 - At least 2 years of experience in the Pharmaceutical or Medical Device Industry.

 - Familiarity with GxP regulatory requirements.

 - Experience in validating computer systems.

 - Knowledge of laboratory systems and processes.

 - Excellent written and verbal communication skills in English.

 - Strong analytical and interpersonal skills.

 - Ability to manage multiple tasks simultaneously.

 - Excellent organizational and management skills.




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.

ІТ-спеціаліст – аналітичні програми

Overview of role
Alvotech is seeking a passionate and skilled&nbsp;Combination Product Lead&nbsp;to join our innovative&nbsp;Combination Products and Devices (CPD)&nbsp;team. The CDP team designs and develops drug delivery solutions that are reliable, accessible, and in keeping with patient needs. The Combination Product Lead works with Human Factors, Risk, Technical, and program strategy specialists to ensure the successful development, verification and validation of our products and maintenance of our combination drug product files (DHFs and DMRs).

We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website. 
We encourage you to visit our Career page (link:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C1203600b68924edbbc5108dce39dd29a%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638635514216949197%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=ZppaZTohYvGV6nMErJd%2Bu4I%2FZ%2B53StVRvXZXohUtTag%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a>) It offers valuable insights into our culture, values, and the innovative work we do. 
Key Responsibilities:
<ul>
<li>Lead the compilation of DHFs, including usability files, design verification testing, and risk assessments.</li>
<li>Draft key deliverables of the design control process.</li>
<li>Collaborate with specialists to deliver design verification, validation, and risk documentation.</li>
<li>Coordinate with regulatory bodies to compile technical files for submission, ensuring compliance with MDR 2017/745 and EU Medical Devices Directive 93/42/EC.</li>
<li>Maintain technical knowledge in the function, assembly, and testing of injection devices.</li>
<li>Stay updated on regulations related to combination drug products.</li>
<li>Author sections of global submission dossiers.</li>
<li>Contribute to process improvements and SOP drafting.</li>
<li>Maintain DHF documentation with QA.</li>
<li>Coordinate document review, updates, and approval for technical projects.</li>
<li>Perform design impact assessments for proposed design changes.</li>
<li>Schedule and manage stage reviews.</li>
</ul>

Qualifications:
<ul>
<li>Master&rsquo;s Degree with a minimum of 7 years of relevant work experience.</li>
<li>Proven experience in life cycle management of combination products.</li>
<li>Strong knowledge of design control processes and regulatory requirements (ISO-13485, ISO-14971, MDR, 21 CFR part 4, ISO-11608, IEC-62366, ASTM 1980, ISO 23908 etc.)</li>
<li>Proficiency in risk management and design verification/validation (ISO-13485, ISO-14971)</li>
<li>Experience with technical documentation and regulatory submissions.</li>
<li>Excellent verbal and written English communication skills.</li>
<li>Ability to work independently and as part of a team.</li>
<li>Self-motivated, adaptable, and positive attitude.</li>
</ul>


Overview of role

Alvotech is seeking a passionate and skilled
Combination Product Lead
to join our innovative
Combination Products and Devices (CPD)
team. The CDP team designs and develops drug delivery solutions that are reliable, accessible, and in keeping with patient needs. The Combination Product Lead works with Human Factors, Risk, Technical, and program strategy specialists to ensure the successful development, verification and validation of our products and maintenance of our combination drug product files (DHFs and DMRs).



We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website.



We encourage you to visit our Career page (link:
Join us - Alvotech - Better Access Better Lives) It offers valuable insights into our culture, values, and the innovative work we do.



Key Responsibilities:


 - Lead the compilation of DHFs, including usability files, design verification testing, and risk assessments.

 - Draft key deliverables of the design control process.

 - Collaborate with specialists to deliver design verification, validation, and risk documentation.

 - Coordinate with regulatory bodies to compile technical files for submission, ensuring compliance with MDR 2017/745 and EU Medical Devices Directive 93/42/EC.

 - Maintain technical knowledge in the function, assembly, and testing of injection devices.

 - Stay updated on regulations related to combination drug products.

 - Author sections of global submission dossiers.

 - Contribute to process improvements and SOP drafting.

 - Maintain DHF documentation with QA.

 - Coordinate document review, updates, and approval for technical projects.

 - Perform design impact assessments for proposed design changes.

 - Schedule and manage stage reviews.




Qualifications:


 - Master’s Degree with a minimum of 7 years of relevant work experience.

 - Proven experience in life cycle management of combination products.

 - Strong knowledge of design control processes and regulatory requirements (ISO-13485, ISO-14971, MDR, 21 CFR part 4, ISO-11608, IEC-62366, ASTM 1980, ISO 23908 etc.)

 - Proficiency in risk management and design verification/validation (ISO-13485, ISO-14971)

 - Experience with technical documentation and regulatory submissions.

 - Excellent verbal and written English communication skills.

 - Ability to work independently and as part of a team.

 - Self-motivated, adaptable, and positive attitude.


Лідер комбінованого продукту

Overview of role:
Join Alvotech as a&nbsp;Pharmacovigilance Manager&nbsp;and become a key player in our mission to deliver safe and effective treatments to patients worldwide. In this dynamic role, you will lead and manage global pharmacovigilance activities, ensuring compliance with international safety standards and regulations. You will work cross-functionally with various departments, including Clinical Development, Patient Safety, Medical Affairs, and Regulatory Affairs, to support all safety-related activities.
Your expertise will be crucial in developing and maintaining our Global PV system, covering both post-marketing pharmacovigilance and clinical safety activities. As a Pharmacovigilance Manager, you will collaborate with internal teams and external partners to ensure the highest standards of safety and quality. This position offers an exciting opportunity to make a significant impact on patient safety and contribute to the success of Alvotech's innovative biosimilar product portfolio. 
We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website. 
We encourage you to visit our Career page (link:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C1203600b68924edbbc5108dce39dd29a%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638635514216949197%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=ZppaZTohYvGV6nMErJd%2Bu4I%2FZ%2B53StVRvXZXohUtTag%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a>) It offers valuable insights into our culture, values, and the innovative work we do. 
Key Responsibilities:
<ul>
<li>Leadership in Pharmacovigilance: Oversee and engage in all PV activities within the Pharmacovigilance department.</li>
<li>Global PV System Management: Develop and manage Alvotech's Global PV system, encompassing both post-marketing and clinical safety activities.</li>
<li>Cross-Functional Collaboration: Work closely with Clinical Development, Patient Safety, Medical Affairs, and other departments to support safety-related activities.</li>
<li>Stakeholder Engagement: Collaborate with internal teams (e.g., Regulatory Affairs, Pharmaceutical Sciences) and external partners (e.g., CROs, service providers) to ensure PV compliance and performance.</li>
<li>Safety Management: Manage post-marketing PV activities for assigned products and clinical safety activities for assigned clinical study programs.</li>
<li>Comprehensive PV Activities: Oversee global pharmacovigilance tasks including ICSR/SAE processing, literature monitoring, signal management, periodic reporting, risk management, and regulatory submissions.</li>
<li>Quality and Compliance: Ensure the PV system is fully compliant with global PV and clinical safety legislation and manage PV audits and inspections.</li>
<li>Training and Development: Deliver training on pharmacovigilance processes and standards to staff and external parties.</li>
</ul>

Qualifications:
<ul>
<li>Education: Master's Degree in pharmaceutical sciences or related fields (medicine, pharmacy, life sciences).</li>
<li>Experience: Minimum of 5 years in the pharmaceutical industry with demonstrable PV knowledge. Experience with biosimilars is a strong advantage.</li>
<li>Technical Skills: Proficiency in safety databases, Microsoft Office tools, and technical software (Adobe, SharePoint, DocuSign, Veeva suite).</li>
<li>Regulatory Knowledge: Detailed understanding of PV processes, directives, regulations, and international guidelines (21CFR, GCP-R3, GVP, ICH, CIOMS etc.).</li>
<li>Communication Skills: Fluent in verbal and written English, with excellent communication and team collaboration skills.</li>
<li>Independence and Accountability: Ability to work independently, manage time effectively, and prioritize tasks.</li>
<li>Positive Work Environment: Maintain a positive, result-oriented work environment and foster a team spirit.</li>
<li>Cultural Adaptability: Ability to work in a multicultural environment and willingness to travel internationally as required.</li>
</ul>


Overview of role:

Join Alvotech as a
Pharmacovigilance Manager
and become a key player in our mission to deliver safe and effective treatments to patients worldwide. In this dynamic role, you will lead and manage global pharmacovigilance activities, ensuring compliance with international safety standards and regulations. You will work cross-functionally with various departments, including Clinical Development, Patient Safety, Medical Affairs, and Regulatory Affairs, to support all safety-related activities.

Your expertise will be crucial in developing and maintaining our Global PV system, covering both post-marketing pharmacovigilance and clinical safety activities. As a Pharmacovigilance Manager, you will collaborate with internal teams and external partners to ensure the highest standards of safety and quality. This position offers an exciting opportunity to make a significant impact on patient safety and contribute to the success of Alvotech's innovative biosimilar product portfolio.



We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website.



We encourage you to visit our Career page (link:
Join us - Alvotech - Better Access Better Lives) It offers valuable insights into our culture, values, and the innovative work we do.



Key Responsibilities:


 - Leadership in Pharmacovigilance: Oversee and engage in all PV activities within the Pharmacovigilance department.

 - Global PV System Management: Develop and manage Alvotech's Global PV system, encompassing both post-marketing and clinical safety activities.

 - Cross-Functional Collaboration: Work closely with Clinical Development, Patient Safety, Medical Affairs, and other departments to support safety-related activities.

 - Stakeholder Engagement: Collaborate with internal teams (e.g., Regulatory Affairs, Pharmaceutical Sciences) and external partners (e.g., CROs, service providers) to ensure PV compliance and performance.

 - Safety Management: Manage post-marketing PV activities for assigned products and clinical safety activities for assigned clinical study programs.

 - Comprehensive PV Activities: Oversee global pharmacovigilance tasks including ICSR/SAE processing, literature monitoring, signal management, periodic reporting, risk management, and regulatory submissions.

 - Quality and Compliance: Ensure the PV system is fully compliant with global PV and clinical safety legislation and manage PV audits and inspections.

 - Training and Development: Deliver training on pharmacovigilance processes and standards to staff and external parties.




Qualifications:


 - Education: Master's Degree in pharmaceutical sciences or related fields (medicine, pharmacy, life sciences).

 - Experience: Minimum of 5 years in the pharmaceutical industry with demonstrable PV knowledge. Experience with biosimilars is a strong advantage.

 - Technical Skills: Proficiency in safety databases, Microsoft Office tools, and technical software (Adobe, SharePoint, DocuSign, Veeva suite).

 - Regulatory Knowledge: Detailed understanding of PV processes, directives, regulations, and international guidelines (21CFR, GCP-R3, GVP, ICH, CIOMS etc.).

 - Communication Skills: Fluent in verbal and written English, with excellent communication and team collaboration skills.

 - Independence and Accountability: Ability to work independently, manage time effectively, and prioritize tasks.

 - Positive Work Environment: Maintain a positive, result-oriented work environment and foster a team spirit.

 - Cultural Adaptability: Ability to work in a multicultural environment and willingness to travel internationally as required.


Менеджер з фармаконагляду

Alvotech is looking for a passionate and skilled Technical Investigator to become a key player in our innovative&nbsp;Combination Products and Devices (CPD) team. In this role you'll lead technical investigations, manage lab operations, and ensure the quality and reliability of our products through data analysis and problem-solving. 
We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website. 
We encourage you to visit our Career page (link:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C1203600b68924edbbc5108dce39dd29a%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638635514216949197%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=ZppaZTohYvGV6nMErJd%2Bu4I%2FZ%2B53StVRvXZXohUtTag%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a>) It offers valuable insights into our culture, values, and the innovative work we do. 
Key Responsibilities:
<ul>
<li>Lead investigations and provide expert technical support within our dynamic technical team.</li>
<li>Periodically operate in R&amp;D laboratory space according to GLP principles.</li>
<li>Propose experiments and interpret data in scientifically and statistically sound manner using standard tools such as Excel, JMP, etc.</li>
<li>Interpret the impact of findings on other programs and actively support product complaint investigations.</li>
<li>Track complaint frequency, evaluate redesign proposals, and lead deviation/OOS investigations.</li>
<li>Offer specialized input into various technical investigations. </li>
</ul>
Qualifications:
<ul>
<li>Bachelor's Degree and a minimum of 5 years of relevant work experience.</li>
<li>Strong background in scientific hypothesis testing and laboratory work.</li>
<li>Excellent verbal and written English communication skills.</li>
<li>Ability to work independently and in a team setting.</li>
<li>Self-motivated, adaptable, and positive attitude.</li>
<li>Requires strong knowledge of Excel and other Microsoft suite software and preference for additional knowledge in at least one of the following: JMP, PowerBI, or Matlab/Octave.</li>
</ul>


Alvotech is looking for a passionate and skilled Technical Investigator to become a key player in our innovative
Combination Products and Devices (CPD) team. In this role you'll lead technical investigations, manage lab operations, and ensure the quality and reliability of our products through data analysis and problem-solving.



We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website.



We encourage you to visit our Career page (link:
Join us - Alvotech - Better Access Better Lives) It offers valuable insights into our culture, values, and the innovative work we do.



Key Responsibilities:


 - Lead investigations and provide expert technical support within our dynamic technical team.

 - Periodically operate in R&amp;D laboratory space according to GLP principles.

 - Propose experiments and interpret data in scientifically and statistically sound manner using standard tools such as Excel, JMP, etc.

 - Interpret the impact of findings on other programs and actively support product complaint investigations.

 - Track complaint frequency, evaluate redesign proposals, and lead deviation/OOS investigations.

 - Offer specialized input into various technical investigations.




Qualifications:


 - Bachelor's Degree and a minimum of 5 years of relevant work experience.

 - Strong background in scientific hypothesis testing and laboratory work.

 - Excellent verbal and written English communication skills.

 - Ability to work independently and in a team setting.

 - Self-motivated, adaptable, and positive attitude.

 - Requires strong knowledge of Excel and other Microsoft suite software and preference for additional knowledge in at least one of the following: JMP, PowerBI, or Matlab/Octave.


Технічний слідчий

Vi&eth; leitum a&eth; lei&eth;toga &iacute;&nbsp;t&aelig;kni&thorn;j&oacute;nustuteymi&nbsp;innan lyfja og l&aelig;kningat&aelig;kja deild hj&aacute; Alvotech (e. Combination Products and Devices). Markmi&eth; deildarinnar er a&eth; &thorn;r&oacute;a v&ouml;rur (a&eth;allega lyfjapenna og sprautur) sem m&aelig;ta &thorn;&ouml;rfum notenda og au&eth;velda &thorn;eim lyfjagj&ouml;f, og standast einnig al&thorn;j&oacute;&eth;legar kr&ouml;fur um &thorn;r&oacute;un lyfja og l&aelig;kningat&aelig;kja. Markmi&eth; t&aelig;kni&thorn;j&oacute;nustuteymisins er a&eth; safna og t&uacute;lka t&aelig;knileg g&ouml;gn um v&ouml;rur &iacute; &thorn;r&oacute;un og jafnframt sty&eth;ja notkun &thorn;eirra &aacute; marka&eth;i. Lei&eth;togi t&aelig;kni&thorn;j&oacute;nustuteymisins vinnur &iacute; n&aacute;nu samstarfi vi&eth; a&eth;rar &thorn;r&oacute;unardeildir og g&aelig;&eth;asvi&eth; til a&eth; greina atvik sem koma geta upp &aacute; marka&eth;i, &thorn;j&aacute;lfa f&oacute;lk &iacute; hvernig v&ouml;rurnar virka, og lei&eth;a t&aelig;knilegar ranns&oacute;knir &thorn;egar &thorn;&ouml;rf er &aacute;. Starfi&eth; krefst reglulegrar vi&eth;veru &iacute; h&ouml;fu&eth;st&ouml;&eth;vum okkar &iacute; Reykjavik.
Vi&eth; bj&oacute;&eth;um upp &aacute; skemmtilegt og krefjandi starf &iacute; al&thorn;j&oacute;&eth;legu umhverfi &aacute;samt fj&ouml;lbreyttum t&aelig;kif&aelig;rum til starfs&thorn;r&oacute;unar. Ef &thorn;&uacute; hefur &aacute;huga &aacute; &thorn;essu spennandi t&aelig;kif&aelig;ri, hvetjum vi&eth; &thorn;ig til a&eth; kynna &thorn;&eacute;r &thorn;a&eth; betur &aacute; heimas&iacute;&eth;u okkar!&nbsp; 
Vi&eth; hvetjum &thorn;ig einnig til a&eth; sko&eth;a starfas&iacute;&eth;una okkar:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C7ae86df454cf4e35e44d08dcd8068404%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638622769693940279%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=DIfyOPk%2BDLdwhPyg%2FbBK9o5hMo%2FcC0yKMZqPozqlCSQ%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a> sem veitir g&oacute;&eth;a inns&yacute;n &iacute; vinnusta&eth;amenninguna, gildin okkar og &thorn;a&eth; frumkv&ouml;&eth;la starf sem vi&eth; st&ouml;ndum fyrir. 
[English]
Overview of role:
Alvotech is seeking a&nbsp;Head of Technical Team&nbsp;to join our innovative&nbsp;Combination Products and Devices (CPD)&nbsp;team. This role is crucial for driving innovation and excellence within our technical team of four dedicated members. The purpose of this team is to provide services to the commercial organization to combination products that have graduated from development, as well as the collection of scientifically and technically sound evidence for design verification of the product during development.
The successful candidate will play a key role in overseeing laboratory setup and conducting experiments in collaboration with the Analytical &amp; Research Development lab,&nbsp;requiring frequent on-site presence&nbsp;in&nbsp;Reykjavik, Iceland.

Key Responsibilities:
<ul>
<li>Lead the CPD technical team, managing laboratory space and ensuring design verification.</li>
<li>Develop and provide training / oversee training on Alvotech products, particularly device attributes and function to stakeholders including complaint handling intake teams (internal and external), deviation investigators, QC testing teams etc.</li>
<li>Develop support service to product complaints team.</li>
<li>Develop support service for unexpected testing event / out of specification event investigations and deviations.</li>
<li>Evaluate and propose redesign opportunities and provide feedback to quality management review board.</li>
<li>Interpret impacts on other programs and support product complaint investigations.</li>
<li>Lead and provide SME input on deviation/OOS investigations.</li>
<li>Apply scientific hypothesis testing and laboratory work expertise.</li>
</ul>

Qualifications:
<ul>
<li>Master&rsquo;s Degree with at least 5 years of relevant experience.</li>
<li>Strong leadership and strategic planning skills.</li>
<li>Excellent decision-making and problem-solving abilities.</li>
<li>High level of independence and accountability.</li>
<li>Broad knowledge of the pharmaceutical value chain.</li>
<li>Experience with internal and external stakeholder engagement.</li>
<li>Ambitious, proactive, and hands-on approach.</li>
<li>Strong team player with a collaborative mindset.</li>
<li>Excellent verbal and written English communication skills.</li>
<li>Service mindset. </li>
</ul>
We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website. 
We encourage you to visit our Career page (link:&nbsp;<a href="https://gbr01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.alvotech.com%2Fcareers&amp;data=05%7C02%7Casgerdurj%40alvotech.com%7C1203600b68924edbbc5108dce39dd29a%7C53cf7bdbb4f949879c325764ef5621ce%7C0%7C0%7C638635514216949197%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=ZppaZTohYvGV6nMErJd%2Bu4I%2FZ%2B53StVRvXZXohUtTag%3D&amp;reserved=0" target="_blank" rel="noopener">Join us - Alvotech - Better Access Better Lives</a>) It offers valuable insights into our culture, values, and the innovative work we do.


Við leitum að leiðtoga í
tækniþjónustuteymi
innan lyfja og lækningatækja deild hjá Alvotech (e. Combination Products and Devices). Markmið deildarinnar er að þróa vörur (aðallega lyfjapenna og sprautur) sem mæta þörfum notenda og auðvelda þeim lyfjagjöf, og standast einnig alþjóðlegar kröfur um þróun lyfja og lækningatækja. Markmið tækniþjónustuteymisins er að safna og túlka tæknileg gögn um vörur í þróun og jafnframt styðja notkun þeirra á markaði. Leiðtogi tækniþjónustuteymisins vinnur í nánu samstarfi við aðrar þróunardeildir og gæðasvið til að greina atvik sem koma geta upp á markaði, þjálfa fólk í hvernig vörurnar virka, og leiða tæknilegar rannsóknir þegar þörf er á. Starfið krefst reglulegrar viðveru í höfuðstöðvum okkar í Reykjavik.

Við bjóðum upp á skemmtilegt og krefjandi starf í alþjóðlegu umhverfi ásamt fjölbreyttum tækifærum til starfsþróunar. Ef þú hefur áhuga á þessu spennandi tækifæri, hvetjum við þig til að kynna þér það betur á heimasíðu okkar!



Við hvetjum þig einnig til að skoða starfasíðuna okkar:
Join us - Alvotech - Better Access Better Lives sem veitir góða innsýn í vinnustaðamenninguna, gildin okkar og það frumkvöðla starf sem við stöndum fyrir.



[English]

Overview of role:

Alvotech is seeking a
Head of Technical Team
to join our innovative
Combination Products and Devices (CPD)
team. This role is crucial for driving innovation and excellence within our technical team of four dedicated members. The purpose of this team is to provide services to the commercial organization to combination products that have graduated from development, as well as the collection of scientifically and technically sound evidence for design verification of the product during development.

The successful candidate will play a key role in overseeing laboratory setup and conducting experiments in collaboration with the Analytical &amp; Research Development lab,
requiring frequent on-site presence
in
Reykjavik, Iceland.



Key Responsibilities:


 - Lead the CPD technical team, managing laboratory space and ensuring design verification.

 - Develop and provide training / oversee training on Alvotech products, particularly device attributes and function to stakeholders including complaint handling intake teams (internal and external), deviation investigators, QC testing teams etc.

 - Develop support service to product complaints team.

 - Develop support service for unexpected testing event / out of specification event investigations and deviations.

 - Evaluate and propose redesign opportunities and provide feedback to quality management review board.

 - Interpret impacts on other programs and support product complaint investigations.

 - Lead and provide SME input on deviation/OOS investigations.

 - Apply scientific hypothesis testing and laboratory work expertise.




Qualifications:


 - Master’s Degree with at least 5 years of relevant experience.

 - Strong leadership and strategic planning skills.

 - Excellent decision-making and problem-solving abilities.

 - High level of independence and accountability.

 - Broad knowledge of the pharmaceutical value chain.

 - Experience with internal and external stakeholder engagement.

 - Ambitious, proactive, and hands-on approach.

 - Strong team player with a collaborative mindset.

 - Excellent verbal and written English communication skills.

 - Service mindset.




We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website.



We encourage you to visit our Career page (link:
Join us - Alvotech - Better Access Better Lives) It offers valuable insights into our culture, values, and the innovative work we do.

Керівник технічної команди

Reporting to QC PRI Team Leader, this is a hands-on laboratory-based position. Employee will participate in QC testing by performing ELISAs, qPCR and ligand binding assays to test for process related impurities and potency of biosimilar products produced at Alvotech.


Reporting to QC PRI Team Leader, this is a hands-on laboratory-based position. Employee will participate in QC testing by performing ELISAs, qPCR and ligand binding assays to test for process related impurities and potency of biosimilar products produced at Alvotech.

Спеціаліст з біологічних аналізів контролю якості – тестування на домішки, пов'язані з процесом

Join our newly formed team within the Quality division at Alvotech, a leading biosimilar pharmaceutical company. As a Specialist in Engineering &amp; CSV Compliance, you will collaborate with various departments to oversee qualification and validation activities for facilities, utilities, and equipment. You will serve as a Quality representative and subject matter expert, ensuring compliance with EU and US legislation for parenteral manufacturing. Your role will involve supporting QA oversight, reviewing and approving qualification documents, change controls, deviations, and CAPAs, and contributing to investigations and corrective actions. We seek a candidate with a bachelor's degree in a relevant area, at least 3 years of experience in the pharmaceutical or medical device industry, and a strong understanding of GAMP 5 guidelines.


Join our newly formed team within the Quality division at Alvotech, a leading biosimilar pharmaceutical company. As a Specialist in Engineering &amp; CSV Compliance, you will collaborate with various departments to oversee qualification and validation activities for facilities, utilities, and equipment. You will serve as a Quality representative and subject matter expert, ensuring compliance with EU and US legislation for parenteral manufacturing. Your role will involve supporting QA oversight, reviewing and approving qualification documents, change controls, deviations, and CAPAs, and contributing to investigations and corrective actions. We seek a candidate with a bachelor's degree in a relevant area, at least 3 years of experience in the pharmaceutical or medical device industry, and a strong understanding of GAMP 5 guidelines.