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Director, MS&T Downstream Laboratory Lead

Job in Gaithersburg, Montgomery County, Maryland, 20883, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-02-08
Job specializations:
  • Engineering
    Biotechnology, Research Scientist, Process Engineer, Quality Engineering
Job Description & How to Apply Below

Role Summary

Director, MS&T Downstream Laboratory Lead, Gaithersburg, US. This role provides scientific and strategic leadership for the Gaithersburg MSAT Downstream Laboratory, collaborates with cross-functional teams to establish and run the downstream MSAT laboratory in support of global programs, and leads hands-on management of the laboratory. The role develops phase-appropriate downstream scale-down models for antibody programs, supports technology transfers and on-market support, and drives scientific rigor and continuous improvement in downstream processes.

Responsibilities
  • Provide scientific and strategic leadership for the Gaithersburg MSAT Downstream Laboratory
  • Collaborate with teams across Supply Chain, Process Development, AS&T, Analytical Development, Quality, and Regulatory to establish and run the downstream MSAT laboratory in support of global programs
  • Provide direct hands-on management of the Gaithersburg MSAT Downstream Laboratory
  • Develop phase-appropriate downstream scale-down models for antibody programs
  • Participate in knowledge and technology transfers for antibody and ADC programs to enable design and execution of downstream characterization, investigational and scale-down model studies to support tech transfers and on-market support
  • Coach and develop MSAT team members on downstream antibody manufacturing processes, laboratory activities and studies
  • Foster a culture of scientific rigor, innovation, and continuous improvement
  • Play a critical leadership role in designing, developing, characterizing, and qualifying downstream processes (including chromatography, filtration, viral inactivation and filtration, UFDF concentration, formulation, and cryopreservation)
  • Draft SOPs, reports, and presentations
  • Maintain and troubleshoot instrumentation and equipment
  • Collaborate with internal and external groups to advance late-stage antibody capabilities
  • Support data analysis and present results within the team and to broader scientific groups
  • Maintain a high standard of good documentation practice, experimentation, and record keeping
  • Work productively in a team environment and independently to deliver against timelines
  • Lead projects, CAPAs, deviations/investigations and/or continuous improvement efforts
  • Support technology transfer to GMP from contract manufacturers or the internal process development team, including process/facility gap assessments and drafting/reviewing GMP documents (batch records, tech transfer protocols, sampling plans)
  • Collaborate closely with downstream tech transfer teams and the Process Validation team to ensure PPQ readiness; contribute to PPQ protocol authoring and review ensuring GMP compliance and scientific rigor
Qualifications
  • Required:

    MS degree in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, or related discipline with 12 plus years of pharmaceutical/biotechnology process development industry experience
  • Required:

    In-depth CMC knowledge in either early or late-stage antibody technology transfer projects with sound understanding of all stages of antibody drug development, GMP, and QbD approach; experience with antibody or ADC on-market technical support is considered a plus
  • Required:

    Proven success leading cross-functional CMC teams and stakeholder/client management
  • Required:

    Strong organizational, troubleshooting, and interpersonal skills along with excellent oral and written communication
  • Required:

    Proven ability to design and perform complex projects while shaping scientific strategy both at the platform and program level
  • Required:

    Proven ability to work independently, effectively plan and organize work activities and prioritize task completion to meet project deadlines
  • Required:

    Demonstrated strategic and enterprise thinking
  • Required:

    Experience as subject matter expert for antibody downstream processes
  • Required:

    Demonstrated collaboration with GMP Manufacturing, Quality Control, Quality Assurance, Engineering, Regulatory Affairs and Process Development within technology transfer projects and product commercialization
  • Preferred:
    PhD
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