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Alvotech · CMO QA, Germany Home office

Sr. Lead

Full-time BioTech
We use cookies to personalise content and ads, to provide social media features and to analyse our traffic. We also share information about your use of our site with our social media, advertising and analytics partners who may combine it with other information that you’ve provided to them or that they’ve collected from your use of their services. You consent to our cookies if you continue to use our website. See our Cookie Policy - Alvotech - Better Access Better Lives Decline Accept Cookies Sign In Search for Jobs Almenn umsókn / General Application CMO QA Sr. Lead page is loaded CMO QA Sr. Lead Apply remote type Fully remote locations Reykjavik Headquarters Lithuania Home Office Germany Home office Greece Home Office Poland Home Office View All 7 Locations time type Full time posted on Posted 7 Days Ago time left to apply End Date: May 4, 2026 (6 days left to apply) job requisition id JR100198 We are looking for a CMO QA Sr. Lead to join Alvotech’s Quality organization. The role is responsible for end‑to‑end Quality oversight of assigned Contract Manufacturing Organizations (CMOs), ensuring compliance with GMP requirements and supporting commercial manufacturing and product supply. Scope & Responsibilities Serve as the single point of contact for consistent product Quality oversight for assigned CMOs Provide Quality support for GMP manufacturing, product release, health authority requirements, and commercial supply Enable efficient communication and decision‑making related to Quality matters with CMOs Ensure timely and accurate Quality communication and delivery of required documentation from CMOs Act as Quality SME and perform review and/or approval of documents and QMS records in line with the RACI matrix Review and/or approve documentation related to technology transfer to CMOs Review and/or approve documentation related to commercial batches, process validation, and master batch records Ensure QMS records related to CMOs are managed in accordance with applicable procedures Support Alvotech and CMO Qualified Persons (QP) in compiling Quality release documentation from CMOs, as required Support compilation and review of APQRs from CMOs as required Review and manage CMO Technical Quality Agreements Job Requirements University degree in Life Sciences, Pharmacy, Engineering, or a related field Proven experience in Quality Assurance within the pharmaceutical or biotech industry Hands‑on experience working with or overseeing Contract Manufacturing Organizations (CMOs) Strong knowledge of GMP, Quality Management Systems, and commercial manufacturing requirements Experience reviewing and approving Quality documentation and agreements Strong communication and stakeholder management skills Highly organized, detail‑oriented, and able to work independently Fluency in 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 well-being 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. Why Alvotech We at Alvotech are passionate about improving lives by increasing access to affordable biologics. We’re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity, and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work, and empowered to succeed in an agile environment. True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds, regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let’s create a healthier world together through affordable biologic medicines. Similar Jobs (2) Associate Scientist, QC Product Testing (Fixed‑Term, 1 Year) locations Reykjavik Headquarters time type Full time posted on Posted 12 Days Ago time left to apply End Date: April 29, 2026 (1 day left to apply) QC Scientists – Analytical (Shift & Daytime Roles) locations Reykjavik Headquarters time type Full time posted on Posted 13 Days Ago time left to apply End Date: April 28, 2026 (11 hours left to apply) About Us At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.   We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.   Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale. If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide. If you have any technical issues, please contact: [email protected] Read More © 2026 Workday, Inc. 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