
501 - 1000 employees
Founded 2013
🧬 Biotechnology
💊 Pharmaceuticals
🏥 Healthcare
💰 $78.3M Post IPO equity on 2025-07
Biotechnology • Pharmaceuticals • Healthcare
Alvotech is a biopharmaceutical company that specializes in developing and manufacturing biosimilars—biologic medicines highly similar to approved reference biologics—to increase global patient access to affordable biologic therapies. The company follows a vertically integrated approach, covering cell line development through fill-and-finish manufacturing, and partners with commercialization experts to bring products to market. Its pipeline includes proposed biosimilars to high-profile biologics, and it emphasizes scale, control and speed in production. Alvotech operates globally and focuses on improving access to biologic medicines.
🔥 25 minutes ago
Where this job comes from
Posted on Alvotech's careers page, not through a job board
First seen by Remote Rocketship 25 minutes ago

501 - 1000 employees
Founded 2013
🧬 Biotechnology
💊 Pharmaceuticals
🏥 Healthcare
💰 $78.3M Post IPO equity on 2025-07
Biotechnology • Pharmaceuticals • Healthcare
Alvotech is a biopharmaceutical company that specializes in developing and manufacturing biosimilars—biologic medicines highly similar to approved reference biologics—to increase global patient access to affordable biologic therapies. The company follows a vertically integrated approach, covering cell line development through fill-and-finish manufacturing, and partners with commercialization experts to bring products to market. Its pipeline includes proposed biosimilars to high-profile biologics, and it emphasizes scale, control and speed in production. Alvotech operates globally and focuses on improving access to biologic medicines.
• Review and critically assess analytical data, studies and technical documentation • Author and review method qualification and validation protocols and reports • Assess and document deviations, unexpected results and out of spec investigations arising during analytical studies • Prepare scientific reports and assessments supporting analytical similarity and comparability, stability, forced degradation and product characterization • Collaborate with laboratory scientists, Quality Assurance, Regulatory Affairs and other technical functions
• Degree in Biology, Biochemistry, Biotechnology, Pharmaceutical Sciences or a related field • Experience in analytical development, qualification or validation, quality control, or related biopharmaceutical activities • Strong knowledge of cell-based potency assays, binding assays, ELISA and related bioanalytical techniques • Strong scientific judgment, data interpretation and technical writing skills • Good understanding of relevant ICH, FDA, USP and GMP requirements • Experience with HCP, residual DNA, residual Protein A or other process-related impurity assays is an advantage
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