Fréttablaðið - 13.01.2018, Blaðsíða 49

Fréttablaðið - 13.01.2018, Blaðsíða 49
Alvotech is a privately owned, fully integrated specialty biopharmaceutical company focused exclusively on development and manufacturing of high quality biosimilar products. We are specialists in biogeneric product creation, all along the value chain from cell line development to commercial manufacturing. Our common goal: to be a global leader in the biosimilar space and to deliver high quality cost competitive products to patients worldwide. We come from all around the world, bringing literally thousands of years of combined knowl- edge and expertise to our mission. ABOUT ALVOTECH Sæmundargötu 15-19, 101 Reykjavík PIONEERING BIOGENERICS DS DEVELOPMENT HUMAN RESOURCES Alvotech is looking to recruit exceptional talents into a rapidly expanding international company. We are focused on creating and developing Pioneering Biogenerics using the knowledge and expertise of our dedicated professionals. Our state-of-the-art facility located in Vatnsmýri in Reykjavík is a testament to our ambition of creating leading quality biogenerics. For us to continue with our exciting projects we need to expand our teams with capable and ambitious talents to join us on our exciting journey. Drug Substance Development Technician Technician DS Development will be working as a part of the process development team who develop a robust upstream process to a target product titre and quality specification. Ability to learn quickly and follow instructions in a controlled enviroment is essential. HR Specialist (temporary position February–November) HR Specialist will develop and implement HR strategies and initiatives aligned with the overall business strategy. The specialist will support employees and managers with HR standards, ensure successful onboarding experience and have overall responsibility of the payroll process. Mass Spectometry Senior Scientist Mass Spectrometry Senior Scientist will be responsible for developing and/or transfer of LC-MS methods to support the development of our biosimilar products, analysis of samples and running and troubleshooting the mass spectometers. Technical Quality Agreements Specialist Specialist TQ Agreements will manage the communication, negotiation and execution of technical quality agreements with contractors, suppliers and service providers for Alvotech as well as being responsible for the creation and management of technical agreement procedure and templates within Alvotech. QA ITANALYTICS IT Validation Specialist The IT validation specialist manages and executes validation and qualification of computer systems and IT infrastructure and furthermore ensures maintained status of validation/qualifica- tion of IT systems. Head of Analytical Development The Head of Analytical Development will lead a group of scientists within Analytical Development supporting biosimilar programs. He/she will define the technical agenda for the ana- lytical development department and ensure alignment of the agenda with the relevant organizational goals. Analytical Development Scientists Analytical Development scientist will develop analytical methods, write method development protocols and reports, analyse samples, report and review data and work on validation of physicochemical methods. Laboratory Technician Laboratory Technician will work in accordance with GMP practices, conducting all activities in a compliant manner and be responsible for receiving samples, sample registration and distribution within the laboratories along with routine checks of laboratory equipment and other tasks within the laboratory. Product Testing Scientists Product Testing Scientist will analyze samples to support raw material, stability and product release testing activities as well as assisting in the preparation of release documentation along with using various analytical techniques for the analysis/release of monoclonal antibodies. Quality Assurance Specialist QA Specialist is responsible for the planning of self-inspections within Alvotech along with recording of observations and corrective actions from self-inspection activities. He/she will assist in data gathering and setup of quality reviews for Alvotech suppliers and proactively identify, assess and incorporate best industry practice and new regulatory guidelines in area of expertise into Alvotech Quality System and SOPs. For further information on all jobs please visit www.alvotech.com. The deadline for applications is the 22nd of January 2018. Please submit CVs and cover letters in English for the application process. DP MANUFACTURING AND DEVELOPMENT Drug Product Development Scientist The DP Development Scientist will manage the pharmaceutical development aspects of a biosimilar development project as a drug product subject-matter-expert in a cross-functional team. He/she will develop and characterize robust manufacturing processes for drug product manufacturing according to QbD principles and internal policies. Drug Product Manufacturing Support DP Manufacturing Support team works in accordance with GMP practices, conducting all activities in a compliant and safe manner. Activities include cleaning and preparing CNC and grade C areas for production along with visual inspection of media filled and product filled final dosage forms. Drug Product Manufacturing Technician DP Manufacturing Technician will carry out all activities required to produce a filled final dosage form, including aseptic filling, line clearances, coding and labeling of filled units, visual inspection as well as ensuring that the clean rooms are maintained in a operational state. The activities will be performed in full compli- ance with cGMP practices. JOIN OUR DYNAMIC TEAM OF EXPERTS 1 3 -0 1 -2 0 1 8 0 4 :3 9 F B 1 2 0 s _ P 0 7 2 K .p 1 .p d f F B 1 2 0 s _ P 0 6 1 K .p 1 .p d f F B 1 2 0 s _ P 0 4 9 K .p 1 .p d f F B 1 2 0 s _ P 0 6 0 K .p 1 .p d f A u to m a tio n P la te re m a k e : 1 E B C -4 F B 0 1 E B C -4 E 7 4 1 E B C -4 D 3 8 1 E B C -4 B F C 2 7 5 X 4 0 0 .0 0 1 4 A F B 1 2 0 s _ 1 2 _ 1 _ 2 0 1 8 C M Y K
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