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Absci

Biopharma protein expression and purification platform

Director Program Management

Program ManagementConfirmed live in the last 24 hours
Full-time$185k - $210k /yrRemote

About the Job

Requirements

  • A bachelor's degree in a scientific, engineering, or technical discipline is required; an advanced degree such as an MS, PhD, or MBA may be considered in an equivalent experience combination.
  • At least 10 years of professional experience in fast-paced biotech environments, including at least 5 years leading drug development programs.
  • A demonstrated track record of delivering with rigor, speed, and accountability in fast-paced biotech organizations.
  • Experience managing drug development programs across discovery, preclinical, and IND-enabling stages; exposure to clinical trial execution and regulatory submissions is strongly preferred.
  • Hands-on ownership of integrated development plans, critical-path management, budgets, and cross-functional resource planning across concurrent programs.
  • Direct experience managing CRO and CDMO execution to schedule, budget, and quality.
  • Ability to lead cross-functional teams and manage senior stakeholders, including executive leadership, governance committees, and alliance partners, driving alignment and decisions without direct authority.
  • Strong command of program management tools and practices, such as MS Project, Smartsheet, portfolio dashboards, and scenario planning, and of drug development processes and milestones.
  • Hands-on experience with agentic AI tools, including AI agents and multi-agent workflows, for program planning, analysis, and reporting.
  • Written and verbal communication skills to distill complexity for senior leadership.
  • Sound judgment, autonomy, and ability to operate effectively in ambiguity in a fast-paced, evolving environment.
  • Legal authorization to work in the United States.

Responsibilities

  • Serve as the dedicated program management partner to a program leader across a portfolio of assets from discovery through IND and clinical entry, including complex, high-risk, and IND-enabling programs.
  • Build and maintain the integrated cross-functional development plan as the source of truth for critical path, scope, timeline, and budget.
  • Apply data-driven planning methods to translate the AI-driven platform's design-build-test-learn cadence into executable, resourced plans, including novel modalities, bespoke IND paths, and first-in-human transitions.
  • Partner with functional leaders to forecast and align program resources and shape development strategy through scenario modeling, milestone forecasting, and resource trade-off analysis.
  • Manage multiple CROs, CDMOs, and other external partners against agreed scope, schedule, budget, and quality standards.
  • Maintain escalation criteria and early-warning thresholds, raise risks early with proposed mitigations, and adapt to reprioritization, negative data, and shifting timelines or resources.
  • Prepare programs for stage-gate and governance reviews; represent programs to the executive team, governance committees, and alliance partners; and support evidence-based decisions, including recommendations to discontinue programs.
  • Maintain portfolio dashboards and provide regular updates on status, spend, and cycle-time metrics, identifying issues with proposed paths forward.
  • Improve program management standards, tools, and planning disciplines; mentor program managers; and support new planning and governance practices.

Desired Qualifications

  • Experience advancing antibody or other biologics programs from discovery through IND.
  • Experience partnering with AI, machine learning, or computational platform teams in drug discovery.
  • Experience in small- to mid-cap or clinical-stage biotech, or in a rapidly scaling organization.
  • PMP, PgMP, or equivalent project/program management certification; Lean or Six Sigma is a plus.
  • Familiarity with GxP requirements and clinical-stage quality expectations.
  • Direct experience managing clinical-stage programs.

About the Company

Absci

Biopharma protein expression and purification platform

AbSci provides biopharma-focused protein expression and biomanufacturing solutions. Its core platform uses a semi-oxidizing cytoplasm and a dual inducible promoter to tightly control protein production, enabling efficient and scalable production of folded, active proteins. A key offering is SoluPure, a chromatography-free purification method that simplifies downstream processing, reducing bottlenecks and costs. Their high-throughput workflow can generate cell lines that produce properly folded proteins in as little as three months, speeding drug development. Compared with traditional systems like CHO mammalian cells, AbSci emphasizes integrating expression and purification with a faster, more cost-effective pipeline and scalable biomanufacturing. The company aims to transform biologics manufacturing by delivering streamlined, high-throughput protein production and purification services to pharmaceutical and biotech customers.

Company size
51-200
Company stage
IPO
Headquarters
Vancouver, WA
Founded
2011

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