Senior Scientist II, CMC BioProcess Purification Development

Company Description

About Abb Vie

Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at  Follow @abbvie on Linked In, Facebook, Instagram, X and You Tube.

The Biologics CMC Development team at Abb Vie in the Bay Area has a long and rich history of biologics development. Located in a state of the art facility in South San Francisco, the team leverages its comprehensive end-to-end CMC capabilities to work collaboratively through all phases of CMC development with a primary focus on advancing complex biologic therapies, such as multi-specifics, and novel modalities, to human clinical studies and eventual licensure.

This role is within a team of highly experienced scientists and managers who have directly enabled the development/IND submissions of 20+ novel biologics and successfully filed two BLAs.

As a member of the CMC Purification Development group, you will apply strong downstream process-development expertise to design robust, phase-appropriate drug substance purification processes for GMP production, clinical studies, and eventual licensure. You will own purification deliverables for assigned programs, help define drug substance development strategy as a functional lead on cross-functional CMC teams, and communicate data-driven recommendations, risks, and tradeoffs to key stakeholders.

This position is an onsite role in a lab-based function. To be successful candidates must enjoy and thrive in a fast-paced and highly collaborative lab environment with daily face-to-face cross-functional interactions between scientists.

Responsibilities

• Develop, optimize, characterize, and scale up purification processes for monoclonal antibodies, multispecifics, antibody‑like molecules, and other complex biologic candidates across early- and late-stage drug substance process development
• Lead technology transfer to internal or external GMP manufacturing sites; author transfer packages, support facility fit and readiness, and provide technical troubleshooting during clinical manufacturing
• Develop viral clearance strategy and oversee studies with contract laboratories, including protocol development, technical review, data interpretation, and report approval
• Optimize purification platforms and deepen process understanding through mechanistic modeling, statistical design of experiments, data analytics, and targeted wet‑lab studies
• Conceive and evaluate novel, advanced bioprocess technologies that are in line with the group’s strategy
• Maintain current scientific knowledge by critically reviewing peer‑reviewed literature, regulatory guidance, patents, and emerging industry trends, and translate relevant advances into program strategy, experimental design, and platform development Seize opportunities to pursue project relevant leads that are in line with the group’s strategy
• Write technical publications,reports, presentations, and regulatory filings including publishing research in peer‑reviewed journals and presenting work at scientific conferences
• Work efficiently,collaboratively,and cross‑functionally to meet project deliverables and timelines.
• Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, and GxP compliance, where applicable
• Mentor and train junior scientists

• Bachelor’s Degree or equivalent education and typically 12+ years of experience, Master’s Degree…