Research Associate

ACL Digital

Philadelphia (Philadelphia County)

On-site

USD 65,000 - 90,000

Full time

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Job summary

ACL Digital is seeking a scientist to perform release, characterization and stability testing of lentiviral products onsite in Philadelphia for a 12-month period. The role involves supporting process development and discovery teams with a range of analytical methods such as Western Blot, ELISA, PCR-based assays, flow cytometry, and viral titration.

The candidate will communicate scientific findings through protocols and reports, and contribute to developing novel methods for quantifying product

Qualifications

  • BS with at least 1 year of relevant experience.
  • Biopharmaceutical industry experience preferred.

Responsibilities

  • Perform release, characterization and stability testing of lentiviral products to support the analytical requirements of the process development and discovery teams, including but not limited to Western Blot, ELISA/Alphalisa, PCR-based methods, flow cytometry, particle analysis, and cell-based viral titration.
  • Communicate scientific data and information effectively through data presentations, protocols, test methods and development reports.
  • Help drive innovative thinking for novel methods to quantitate lentiviral product strength, safety, purity, and identity.

Skills

Communication skills
Team player
Attention to detail

Education

Bachelor's degree

Job description

Location: Philadelphia, PA (Onsite, 5 days)

Duration: 12 months

Job Responsibilities
  • Perform release, characterization and stability testing of lentiviral products to support the analytical requirements of the process development and discovery teams, including but not limited to Western Blot, ELISA/Alphalisa, PCR-based methods, flow cytometry, particle analysis, and cell-based viral titration.
  • Communicate scientific data and information effectively through data presentations, protocols, test methods and development reports.
  • Help drive innovative thinking for novel methods to quantitate lentiviral product strength, safety, purity, and identity.
Basic Requirements

BS with at least 1 years of relevant experience Biopharmaceutical Industry experience preferred

Preferred Qualifications
  • Demonstrated competency and experience with characterization of viral vectors using cell-based, molecular (qPCR/ddPCR) and/or traditional biochemical methods.
  • Experience developing procedures for use in GLP and/or cGMP facilities is ideal.
  • Effective communication skills and collaborative skills are required.
  • Strong commitment to on-the-bench experimental work
  • A strong team player with excellent oral and written communication skills; to design, execute and troubleshoot experiments with limited oversight; and analyze, interpret, and clearly communicate complex analytical data.
  • Highly organized with a strong attention to detail, able to work in a timeline-driven, fast-paced and highly collaborative working environment.
  • Working knowledge and proficiency with Microsoft Office software.
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