Alvotech is currently seeking a highly skilled and experienced Quality Control Laboratory Manager to join our team in Reykjavik. This role involves a high degree of responsibility and demands a comprehensive understanding of various analytical techniques and methods. If you're seeking an exciting role where you can utilize your expertise and significantly impact product testing and stability, this opportunity is for you.

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

Alvotech hf

<ul>
<li>Management and oversight of all QC laboratories within the Quality Control</li>
<li>Be responsible for all GMP compliance aspects of the labs, including equipment, employees, supplies, and documentation.</li>
<li>Be responsible for the safe and efficient running of the Quality Control/Analytical laboratory.</li>
<li>Review and approve generated technical documentation within the document management system</li>
<li>Maintain regulatory readiness, participate actively in regulatory preparation and inspections</li>
<li>Provide oversight and technical guidance, ensuring an optimal level of scientific ability and training within the department</li>
<li>Identify required document changes and empower staff to implement changes promptly</li>
<li>Collaborate with fellow Managers and Team Leaders on departmental initiatives</li>
</ul>

Helstu verkefni og ábyrgð

<ul>
<li>BS/M.Sc in a relevant scientific discipline</li>
<li>5+ years of experience in biotech or pharmaceutical industry</li>
<li>Demonstrated scientific and leadership skills. Experience leading teams of scientists with varying levels of experience is required.</li>
<li>Good conceptual, analytical, problem-solving, and organizational skills &ndash; must be detail-oriented, well-organized, and able to work independently and in teams</li>
</ul>

Menntunar- og hæfniskröfur

<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>

Fríðindi í starfi


Alvotech is currently seeking a highly skilled and experienced Quality Control Laboratory Manager to join our team in Reykjavik. This role involves a high degree of responsibility and demands a comprehensive understanding of various analytical techniques and methods. If you're seeking an exciting role where you can utilize your expertise and significantly impact product testing and stability, this opportunity is for you.

Ended

QC Laboratory Manager

Alvotech is seeking a dedicated cell culture scientist to join our Upstream Process (USP) Research and Development (R&amp;D) team. As a USP scientist, you will play a crucial role in our USP team developing a small-scale bioreactor process for subsequent scale-up and transfer to a manufacturing environment for production of biosimilars.


Alvotech is seeking a dedicated cell culture scientist to join our Upstream Process (USP) Research and Development (R&amp;D) team. As a USP scientist, you will play a crucial role in our USP team developing a small-scale bioreactor process for subsequent scale-up and transfer to a manufacturing environment for production of biosimilars.
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

Upstream Process Development (R&D) - Scientist

We are looking for a motivated Scientist to join the Process Related Impurity (PRI) team within the Analytical Research and Development (ARD) department at Alvotech, Reykjavik. In this position, you will be a part of an agile team with the focus on analyzing samples, method development and validation of process impurity assays for biologics (biosimilar).
The ARD department consists of dedicated scientists, working with a great variety of analytical assays, including cell-based and process impurity assays, applied to analyze samples from process development groups and manufacturing.
We offer an exciting working environment with a unique opportunity for personal and scientific growth for both experienced and recently graduated scientists.


We are looking for a motivated Scientist to join the Process Related Impurity (PRI) team within the Analytical Research and Development (ARD) department at Alvotech, Reykjavik. In this position, you will be a part of an agile team with the focus on analyzing samples, method development and validation of process impurity assays for biologics (biosimilar).

The ARD department consists of dedicated scientists, working with a great variety of analytical assays, including cell-based and process impurity assays, applied to analyze samples from process development groups and manufacturing.

We offer an exciting working environment with a unique opportunity for personal and scientific growth for both experienced and recently graduated scientists.
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.

Scientist for Process Related Impurity Testing

Alvotech is seeking a dedicated and detail-oriented Research and Development (R&amp;D) Technician to support our innovative R&amp;D team. As an R&amp;D Technician, you will play a crucial role in maintaining the efficiency and effectiveness of our R&amp;D operations. You&rsquo;ll be part of the lab management team, ensuring that our R&amp;D departments run smoothly by managing key supporting activities.


Alvotech is seeking a dedicated and detail-oriented Research and Development (R&amp;D) Technician to support our innovative R&amp;D team. As an R&amp;D Technician, you will play a crucial role in maintaining the efficiency and effectiveness of our R&amp;D operations. You’ll be part of the lab management team, ensuring that our R&amp;D departments run smoothly by managing key supporting activities.
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.

R&D Technician

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The Purchasing Manager is responsible for all purchasing activities of raw materials, components, equipment, and services essential for Alvotech&rsquo;s operation. This involves managing the operational purchasing process, ensuring the timely placement of purchase orders, on-time deliveries, and effective inventory management.&nbsp;
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The Purchasing Manager is responsible for all purchasing activities of raw materials, components, equipment, and services essential for Alvotech’s operation. This involves managing the operational purchasing process, ensuring the timely placement of purchase orders, on-time deliveries, and effective inventory management.










Purchasing Manager 

The QC Product Testing Shift Lead in the Microbiology Lab is responsible for overseeing the microbiological testing operations during their assigned shift. This role ensures that all testing activities related to microbial analysis are conducted accurately, efficiently, and in compliance with regulatory standards, particularly Good Manufacturing Practices (GMP). The Shift Lead plays a crucial role in ensuring product safety by monitoring and managing microbial testing processes, coordinating team efforts, and ensuring that all laboratory activities meet stringent quality standards.


The QC Product Testing Shift Lead in the Microbiology Lab is responsible for overseeing the microbiological testing operations during their assigned shift. This role ensures that all testing activities related to microbial analysis are conducted accurately, efficiently, and in compliance with regulatory standards, particularly Good Manufacturing Practices (GMP). The Shift Lead plays a crucial role in ensuring product safety by monitoring and managing microbial testing processes, coordinating team efforts, and ensuring that all laboratory activities meet stringent quality standards.