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AskBio

Clinical-stage gene therapy company developing AAVs

Manufacturing Specialist 2 - DNA

Bioprocess & BiomanufacturingPosted on Nov 11
Full-timeDurham, NC, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a biological or engineering discipline with 2+ years of relevant work experience, a master's degree in a biological or engineering discipline, or a high school diploma with 6+ years of role-relevant work experience is required.
  • Experience or demonstrated skills with one or more of the following techniques: aseptic technique; preparing reagents at desired dilutions or concentrations; restriction enzyme digestion; gel electrophoresis; DNA quantitation; identifying annotated features on a plasmid map; bacterial cell culture; centrifugation; filtration; fermentation; and liquid chromatography.
  • Strong attention to detail, organization, and ability to multitask in a fast-paced, highly interactive team environment are required.
  • A track record of independently delivering and interpreting experimental results is required.
  • Verbal and written communication skills, formal record-keeping ability, and ability to interact effectively with internal and external stakeholders are required.
  • Ability to work and learn in a fast-paced, team-oriented laboratory environment is required.
  • Experience with laboratory management, fermentation, and molecular biology or DNA sequence design and analysis software is required.

Responsibilities

  • Perform hands-on plasmid purifications to support research-grade rAAV manufacturing, technology improvements, and progression of early-stage gene therapy programs.
  • Follow batch records and document method procedures in a detailed, organized manner.
  • Perform and evaluate data analysis at completion of test methods, summarize results, and finalize batch records.
  • Independently support process investigations, improvements, and optimization activities in collaboration with Senior Research Associates and the DNA Process Development group.
  • Identify, develop, and implement process improvements, including revisions to standard operating procedures, batch records, analytical records, and formulation records, and initiate new procedures when necessary.
  • Manage inventory of raw materials and laboratory supplies.
  • Prepare manufacturing reports and data to present to scientists and management.
  • Ensure laboratory areas are clean and organized, and ensure equipment, supplies, and raw materials are available and ready for use.

Desired Qualifications

  • A master's degree in a biological or engineering discipline is preferred.
  • Experience with fermentation is preferred.
  • Experience with SnapGene is preferred.

About the Company

AskBio

Clinical-stage gene therapy company developing AAVs

AskBio develops adeno-associated virus (AAV) gene therapies for genetic and complex diseases. Therapies use AAV vectors to deliver therapeutic genes into patients’ cells and move through research, clinical trials, and toward commercialization. It differentiates itself with a clinical-stage portfolio and a partnerships-based model, combining in-house R&D with licensing deals. Its goal is to bring gene therapies to patients with unmet medical needs by advancing candidates through development and into the market.

Company size
501-1,000
Company stage
Acquired
Total funding
$239.1M
Headquarters
Durham, NC
Founded
2001

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