Associate Director, CMC Program Management

Job not on LinkedIn

November 7

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Logo of Vera Therapeutics, Inc.

Vera Therapeutics, Inc.

Biotechnology • Pharmaceuticals

Vera Therapeutics, Inc. is a clinical-stage biotechnology company focused on developing treatments for immunological kidney diseases that improve patients’ lives. The company is advancing Atacicept through clinical development for IgA nephropathy (IgAN), running Phase 2b and Phase 3 trials, and pursuing programs in lupus nephritis and other immunologic conditions. Headquartered in Brisbane, CA, Vera emphasizes science-driven drug development, patient engagement, and sustainability.

201 - 500 employees

🧬 Biotechnology

đź’Š Pharmaceuticals

đź“‹ Description

• Develop, maintain, and track project timelines and deliverables for CMC activities, ensuring alignment with organizational and departmental objectives. • Coordinate commercial supply readiness and next generation process development activities across CMC, quality, regulatory, commercial, and external CDMO/CMOs. • Act as a liaison between CMC team and external partners, consolidate and disseminate key decisions and updates across cross-functional workstreams. • Support CMC Subteam and other governance forums to develop, track and execute on CMC functional objectives and lifecycle management initiatives. • Work with CMC team to develop, manage and track the CMC budget. • Provide CMC project management support, both internally and externally with vendors. This includes activities such as drug substance/drug product development, manufacturing, and supply chain oversight. Proactively track and manage activities at vendors and facilitate resolution of issues to keep project activities on track. • Create and maintain program management tools to communicate timelines, deliverables, issues, risks, and mitigations. Ensure cross functional alignment on program status including expectations, opportunities, and risks.

🎯 Requirements

• BS/MS degree in a scientific or engineering discipline. PMP is a plus. • 8 years of biotech experience in any of the following sub-disciplines; process development, manufacturing, and/or analytical development. • 5 years of CMC program management experience. • Proficient in Microsoft Project. • Experience in Smartsheet is preferred but not required • High level of attention to detail. • Ability to work with ambiguity, and create new, more efficient processes; desire to bring order and organization to a newly developing organization • Ability to communicate effectively with stakeholders across the organization at all levels. • Proven ability to manage competing priorities, budgets, and timelines in a fast-paced, rapid-growth environment. • Highly skilled at working collaboratively with cross-functional teams and contractors to drive results and meet company objectives. • Excellent written and verbal communication skills, including a demonstrated ability to effectively communicate in a program team environment, within department, among functional groups, and external collaborators. • Self-directed and proactive with ability to function independently, exercise good judgment, and respond quickly and effectively to changing environments.

🏖️ Benefits

• Equal-opportunity employer • Fair and equitable compensation practices • Total compensation packages that are market competitive

Apply Now

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