Við hjá Alvotech vinnum að því að þróa og framleiða líftæknilyf sem geta bætt líf og heilsu milljóna manna um allan heim. Markmiðið er að vera á meðal fremstu fyrirtækja í framleiðslu og sölu hliðstæðulyfja á viðráðanlegu verði og gera þau þannig aðgengilegri fyrir fólk sem annars hefði ekki ráð á þeim.
Við höfum byggt upp fjölþjóðlegt fyrirtæki í hjarta Reykjavíkur með 450 starfsmenn frá yfir 50 þjóðlöndum þar sem áhersla er lögð á jafnrétti og fjölbreytileika. Unnið er að stækkun húsnæðis hátækniseturs Alvotech í Vatnsmýrinni og undirbúningi á framleiðslu og sölu líftæknilyfja.
Starfsumhverfi fyrirtækisins einkennist af drifkrafti, ástríðu, heilindum og fagmennsku. Það eru spennandi tímar framundan og við leitum að samstarfsfólki sem brennur fyrir að bæta líf fólks um heim allan.
Alvotech er stolt af því að hafa hlotið Jafnlaunavottun Jafnréttisstofu Íslands.
Viltu vera með?
Gæðadeildir // Quality
Scientist QC Raw Materials
The Scientist in Quality Control (QC) Raw Materials (RM) is responsible for the inspection, sampling and testing of incoming goods to be used in the manufacturing process, as well as performing routine cleaning, inspections, and upkeep of laboratory equipment.
Particle Testing Scientist QC Raw materials
The Particle Testing Scientist is responsible for developing methods and procedures for particle controls packaging components, as well as supporting particle related investigations.
Visual Inspection Scientist QC Raw Materials
The Visual Inspection Scientist is responsible for the release of incoming goods for the manufacturing process at Alvotech. The role involves information gathering, establishing work documents, the setup of inspection libraries and laboratory testing.
Quality Management Specialist
The Quality Management (QM) Specialist is responsible for collecting, analysing, and reporting metrics from across Alvotech, in addition to monitoring and reporting on the status of actions from regulatory inspections, partner audits, self-inspections, QM reviews and the Alvotech Quality Plan.
Specialist Technical Quality Agreements
The Technical Quality Agreement Specialist will assist Quality Assurance (QA) in streamlining the TQA process, driving eciency and improvements.
QA Specialist DP Manufacturing
The QA Specialist is responsible for supporting drug product manufacturing.
The main responsibilities will be the review and approval of batch records, investigations, and quality documents.
QC Sample Management Scientist
The QC Sample Management Scientist performs daily tasks like aliquoting, pulling of stability samples and sample shipments. Performs routine analytical work with advanced analytical techniques, creates and updates documents for methods and raw materials and reviews results of simple methods.
QC Product Testing Scientist
The QC Product Testing Scientist actively participates in quality control and release of product manufactured at Alvotech. Performs routine analytical work with advanced analytical techniques. Creates and updates documents for methods and raw materials, reviews results of simple methods.
Rannsóknir og Þróun // Research & Development
Downstream Development Scientist (Entry Level)
The Downstream Development Scientist’s role consists of lab support tasks, including solution preparation, running chromatography and crossflow systems, maintaining the equipment and lab responsibly, in addition to executing experiments in all DSPD unit operations.
Downstream Development Scientist
The Downstream Development Scientist is responsible for designing fit-for-purpose purification experiments, as well as compiling and analysing experimental data to generate process knowledge and support global regulatory submission.
Scientists Drug Product Development
We have three Drug Development Scientist positions available in the Drug Product Development team working on the development of liquid/lyophilized biologics (biosimilar) manufacturing processes. The positions are in: Formulation development, Process development and Material science.
Bioassay Development Scientist
The Bioassay Development Scientist performs method development, qualification, validation and testing of a process impurity assays, such as residual protein A ELISA, residual DNA (qPCR) and residual HCP ELISA assays. The scientist creates method development, qualification protocols and reports.
Lyfjaframleiðsla // Manufacturing
Drug Product Manufacturing Technician
The Drug Product Manufacturing Technician level III performs all manufacturing activities in Drug Production with a focus on “clean room” behaviour, provides guidance and training, identifies process improvement, and helps create and maintain a lean, flexible and agile manufacturing facility
Head of Commissioning and Qualification
The Head of Commissioning and Qualification (C&Q) is responsible for leading the C&Q team in Technical Operations and is responsible for organizing, scheduling, and coordinating team eorts and supporting various departments within Alvotech for C&Q purposes.
Upplýsingatækni // Information Technology
IT Application Administrator
The IT Application Administrator is a member of the Computer System Management (CSM) team in IT. The CSM team is responsible for the implementation, operation, and administration of computer systems, in a highly regulated environment.
IT Compliance Specialist
The IT Compliance Specialist supports the life cycle management of computerized systems ensuring compliance with regulatory requirements and participates in the continuous improvement of IT policies and procedures.
Innkaup // Procurement
Strategic Sourcing Specialist
The Strategic Sourcing Specialist manages specific procurement categories, both direct and indirect, to achieve added value from the supplier market and direct savings, in addition to negotiating favourable procurement contracts with selected vendors and suppliers and creating and maintaining key performance indicator (KPI) metrics for supply chain performance.
Tactical Purchase Specialist
The Tactical Purchase (TP) Specialist role entails order management, including control of the Alvotech Purchase Order Process. The TP specialist works with end users to define needs, optimize sourcing and purchase activities, assuring seamless availability of materials to support company objectives.
Alvotech er alþjóðlegt fyrirtæki og samskiptamál okkar er enska.
Frekari upplýsingar um þessi störf og fleiri er að finna á vefnum okkar.
For more information visit www.alvotech.com
Merkja við auglýsingu
Þú þarft að skrá þig inn til að vista þessa auglýsingu
Sækja um starf
Til að sækja um þetta starf, vinsamlega farðu á jobs.50skills.com.