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
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