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Dir​/Sr. Director, Upstream Biologics Manufacturing

Job in Chesterbrook, Chester County, Pennsylvania, USA
Listing for: Avalo Therapeutics
Full Time position
Listed on 2026-09-07
Job specializations:
  • Manufacturing / Production
    Validation Engineer, Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 180000 - 240000 USD Yearly USD 180000.00 240000.00 YEAR
Job Description & How to Apply Below
Position: Dir./Sr. Director, Upstream Biologics Manufacturing
Location: Chesterbrook

Chesterbrook, PA

At Avalo (ahh-vah'-low), we are 100% focused on developing treatments for immune-mediated inflammatory diseases with large unmet needs that affect millions worldwide. Our strategy is to develop medicines that target the IL-1β pathway, which is a central driver of the inflammatory process.

We share a commitment to teamwork, passion for science, and dedication to patients suffering from acute and chronic inflammatory disorders. Our collective expertise in discovery, development, and regulatory approvals is evidenced in our strong individual track records of advancing multiple therapeutic programs to successful commercialization.

Position Summary

The Dir./ Sr. Director, Upstream Biologics Manufacturing will provide technical and strategic leadership for outsourced upstream drug substance manufacturing, with primary responsibility for supporting late-stage clinical development and advancing biologics manufacturing processes toward commercial readiness. This individual will serve as the Company's upstream manufacturing subject matter expert and primary technical representative with Contract Development and Manufacturing Organizations (CDMOs/CMOs), ensuring reliable clinical supply while driving manufacturing execution, process characterization, technology transfer, process validation/PPQ, continued process verification, regulatory inspection readiness efforts, and preparation for commercial manufacturing.

The Dir./Sr. Director will serve as the upstream process SME across development, manufacturing, and partner closely with internal and consultant CMC resources, Quality, Regulatory Affairs, Supply Chain, Program Management, and external manufacturing partners to ensure robust, compliant, scalable, and reliable production of biologic drug substance. The role requires strong technical judgment, ownership, and the ability to influence and drive results in a highly outsourced operating model.

Essential Duties and Responsibilities External Manufacturing Leadership
  • Serve as the technical lead and Company subject matter expert for upstream manufacturing activities performed at external CDMOs.
  • Lead the technical evaluation, selection, qualification, governance, and ongoing performance management of upstream CDMO partners.
  • Provide oversight of mammalian cell culture-based manufacturing processes from cell bank/seed train expansion through bioreactor production and harvest.
  • Review manufacturing readiness, campaign plans, batch records, production schedules, process performance, and manufacturing data to ensure successful execution.
  • Establish strong technical relationships with CDMO process development, manufacturing, quality, engineering, and project management teams; appropriately challenge and elevate technical or execution risks.
  • Provide technical input to scopes of work, manufacturing agreements, change orders, and contract discussions related to process requirements and CDMO capabilities.
Process Monitoring and Technical Support
  • Review and assess batch records, process trends, deviations, investigations, and manufacturing performance data.
  • Lead technical troubleshooting during manufacturing campaigns and drive or support root-cause investigations for process deviations, non-conformances, and unexpected manufacturing performance.
  • Evaluate process performance metrics, including:
  • Cell growth and viability
  • Metabolite profiles
  • Process yields
  • Product quality attributes
  • Process robustness and consistency
  • Identify and implement appropriate process improvements while maintaining alignment with late-stage development, comparability, validation, and regulatory requirements.
Technology Transfer and Process Validation
  • Avalo SME will lead the evaluation and implementation of upstream aspects of process transfers between development laboratories, pilot facilities, and commercial manufacturing sites at CDMO’s.
  • Support development and review of technology transfer packages, process descriptions, risk assessments, and comparability protocols.
  • Provide technical oversight during engineering, demonstration, PPQ, and validation batches. Evaluate process performance data and recommend process improvements to increase reliability,…
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