Receival and distribution of external/internal samples
Support in management of stability studies within the sample management team
Notifying manager of identified deviations
Complete master laboratory records documentation using good documentation practices
Support in sample management tasks such as reconciliation of log books and discarding measured/backup samples
Be aware of preparations for regulatory inspections
Be aware of and comply with Alvotech’s current EHS policies
Job requirements:
Bachelor’s degree and 1-3 years of relevant work experience in the pharmaceutical or biopharmaceutical sector.
Proficient in using a PC and common Microsoft packages such as Word and Excel.
Basic Knowledge of Good Manufacturing Practices (GMP) and documentation Rules is an asset.
Communication skills: Excellent technical written and verbal communication skills.
Very good command of English, both written and spoken.
What we offer:
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.
The chance to be a part of a global and fast-growing company.
An international work culture that encourages diversity, collaboration and inclusion.
Positive, flexible, and innovative work environment.
Support for personal growth and internal career development.
Company social events and milestone celebrations.
Excellent in-house canteen and coffee house.
Exercise and wellbeing support for full-time employees.
On-site shower facility.
Transportation grant towards eco-friendly modes of travel for full-time employees.
Internet at home for full-time employees.
About Alvotech
Our mission is to improve patient lives and the sustainability of the global healthcare ecosystem by broadening the availability and accessibility of biosimilars.