
Alvotech hf
Alvotech er fjölþjóðlegt hátæknifyrirtæki í fremstu röð. Meira en 1400 starfsfólk af um 70 þjóðernum sameinast um að móta framtíðina á sviði líftæknilyfja og tryggja sjúklingum um allan heim betra aðgengi að hágæða lyfjum. Meðal starfsfólks eru margir af færustu vísindamönnum landsins.
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 alls starfsfólks, 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.

QC Compliance Scientist
Quality control Reykjavik is seeking a compliance specialist supporting maintenance of GMP compliance in the quality control unit. You will work together with a team of more than 70 people to ensure the quality of medicines produced at Alvotech by helping to perform the work of the team according to GMP regulations.
Menntunar- og hæfniskröfur
Bachelor's or master's degree in the field of analytical chemistry, biochemistry, biotechnology, or similar
Experience in the biopharmaceutical industry > 3 years
Analytical biopharmaceutical experience (Development, validation, and application of analytical methods in a GMP environment) > three years
Good knowledge of spoken and written English
Strong communication and organization skills, self-motivation, and good team skills
Confident in using MS Office (Word, Excel, and PowerPoint)
Helstu verkefni og ábyrgð
Monitor the status of all types of quality records like deviations, change controls, corrective and preventive actions, and change actions
Support closure of quality records actively either supporting by managing subject matter experts or as a subject matter expert
Perform walkthroughs to check compliance in the QC laboratories
Perform training on compliance topics
Compile and update compliance-related QC SOPs
Act as SME for compliance topics in inspections
·Prepare, support, and follow up on audits
Fríðindi í starfi
The chance to be a part of a global and fast-growing company.
Support for personal growth and internal career development.
Excellent in-house canteen and coffee house.
On-site shower facility.
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.
Company social events and milestone celebrations.
Exercise and well-being support for full-time employees.
Positive, flexible, and innovative work environment.
Transportation grant towards eco-friendly modes of travel for full-time employees.
Internet at home for full-time employees.
An international work culture that encourages diversity, collaboration, and inclusion.
Auglýsing birt24. nóvember 2022
Umsóknarfrestur10. desember 2022
Tungumálahæfni
Engar sérstakar tungumálakröfur
Staðsetning
Sæmundargata 15-19 15R, 101 Reykjavík
Starfstegund
Starfsgreinar
Starfsmerkingar
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