Senior Scientist, Process Development (Contract)

Adverum Biotechnologies, Inc.Redwood City, CA
3d$60 - $70

About The Position

Adverum, a wholly owned subsidiary of Eli Lilly and Company, is looking for a Senior Scientist to join our Process Development team in Redwood City. This individual will be a key member of the team, focusing on downstream activities. This is a 12-month contract with an opportunity for an extension.

Requirements

  • Bachelor’s or advanced degree in chemical/biochemical engineering or related fields.
  • 6-8 years of downstream purification experience in pharmaceutical or gene therapy manufacturing, including GMP-regulated operations.
  • Hands on experience with buffer preparations, TFF (Hollow Fiber/Cassettes), UF/DF and Column Chromatography Purification. Experience working with AKTA Avant is required.
  • Able to work in a fast-paced environment as a team player with effective communication skills.
  • Excellent computer skills; especially proficient in Excel and Word.
  • Strong desire to learn new technologies, skill sets, and science behind AAV processing.
  • Strong teamwork and communication skills.

Nice To Haves

  • Experience with statistical analysis software (e.g., JMP) and data visualization tools is a plus.
  • Familiarity with regulatory guidelines and requirements for biologics manufacturing is a plus.

Responsibilities

  • Perform pilot scale downstream purification process and manufacturing (post cell lysate to final formulation) by utilizing column chromatography, UFDF, and various filtration steps.
  • Follow good documentation practices to maintain accurate records.
  • Work closely with team members to perform buffer preparation.
  • Set-up, operate and maintain required downstream laboratory equipment.
  • Maintain reagent, sample, and consumables inventory.
  • Assist with data entry and data analysis in Excel and/or other statistical programs.
  • Ensure safe workplace in compliance with the company and EHS' rules and regulations.
  • Work with Assay Development and Quality Control to coordinate testing.
  • Work to optimize, and revise current process protocols, procedures, and batch records to make them more robust and streamlined.
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