Senior Global AS&T Specialist

AskBioDurham, NC
Onsite

About The Position

This role is a secondment opportunity at AskBio, a company focused on advancing gene therapy. The Senior Global Analytical Sciences and Technology (AS&T) Specialist will support analytical method lifecycle management, troubleshooting, and method transfer activities for gene therapy products. This position requires the ability to work effectively in a matrix organization and influence without direct authority. The role is office-based in RTP, NC and reports to the Director, Analytical Sciences.

Requirements

  • Bachelor’s degree in biology, microbiology, molecular biology, biotechnology or related field with 5+ years of relevant work experience, or a Master’s degree with 2+ years of relevant work experience.
  • Demonstrated experience working in matrix organizations and independent management of cross-functional initiatives.
  • Ability to influence without direct authority across teams and functions.
  • Hands-on experience supporting GMP environments.
  • Experience with method validation, transfer, and lifecycle management.
  • Knowledge of analytical methods supporting biologics manufacturing.
  • Understanding ICH, FDA, and EMA requirements for gene therapy products.
  • Excellent written and verbal communication skills.
  • High attention to detail and data integrity mindset.
  • Strong problem-solving and investigative skills.

Nice To Haves

  • Industry experience with strong focus on gene therapies analytical methodologies.
  • Experience with stability studies and impurity profiling.
  • Project management and prioritization skills.
  • Experience supporting regulatory filings and agency interactions.
  • Knowledge of Quality by Design (QbD) and risk-based approaches.

Responsibilities

  • Develop and implement phase appropriate analytical control strategies for gene therapy products.
  • Participate in lifecycle management of complex bioanalytical methods, including PCR/ddPCR, ELISA, cell-based potency assays, NGS, HPLC, and AUC.
  • Support method qualification, validation, and comparability studies for rAAV program methods.
  • Analyze analytical data across programs to identify trends, method variability, and product consistency.
  • Apply statistical tools to evaluate assay performance and capability.
  • Drive continuous improvement initiatives for analytical technologies, including digitalization and automation.
  • Participate in or lead analytical method transfers to/from CDMOs, CROs, and internal QC laboratories.
  • Author and approve transfer protocols, validation documents, and technical reports.
  • Act as the AS&T SME for external partners, ensuring alignment on method performance and expectations.
  • Troubleshoot cross-site method activities, ensuring consistency across global networks.
  • Support investigations (OOS/OOT/deviations) and assist in determination of root cause analysis of complex analytical methods.
  • Partner with Quality to define and implement CAPAs and ensure inspection-readiness.
  • Author and review analytical sections of regulatory submissions (IND, BLA, MAA), with emphasis on gene therapy requirements.
  • Ensure analytical control strategies align with evolving regulatory expectations for advanced therapies.
  • Support regulatory interactions, inspections, and responses as an analytical SME.

Benefits

  • Secondment opportunity to broaden experience, expand knowledge, and contribute to AskBio’s mission.
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