Quality Control Analyst II

in Pharma Contract

Job Detail

  • Experience Level Mid Level
  • Degree Type Bachelor of Science (BS)
  • Employment Consulting
  • Working Type On Site
  • Job Reference 0000009139
  • Salary Type Hourly
  • Industry Pharmaceuticals
  • Selling Points

    Opportunity to work for biopharma company focused on developing rare disease treatments.

Job Description

Quality Control Analyst II – Molecular Virology

1 year initial contract

Position Summary

 

Reporting to the Director, QC Cellular Virology & Molecular Biology, the Analyst II – QC Molecular Biology will support the gene therapy program pipeline including but not limited to routine GMP testing of AAV vector analytical methods such as GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed. Adaptable to perform in a fast-paced environment while still delivering high-quality results, this Analyst II – QC Molecular Biology will be required to have strong interpersonal skills and be able to work under minimal supervision. 

 

This role typically requires that the majority of the work be conducted on-site and thus will be subject to certain on-site safety protocols. 

 

Responsibilities

·        Perform routine QC testing including, but not limited to: ddPCR/dPCR and qPCR test methods in support of in-process, release, and stability.

·        Support routine laboratory operations (equipment cleaning, laboratory cleaning, inventory control, logbook management).

·        Support development, technical transfer and validation of qPCR and dPCR-based assays and other methods for lot release and stability as needed.

·        Author and revise SOPs/Forms and other relevant controlled documentation.

·        Perform peer review of both internally and externally generated data.

·        Support QC deviations. Investigations, analytical method performance trending and root cause analysis, as needed.

 

·        Ensures laboratory inspection readiness and assists with Troubleshooting/continuous improvement as needed.

Requirements

o   BS or MS in Molecular Biology, Cell Biology, Biochemistry or a related discipline with 2+ years industry experience. QC GMP experience is required.

o   Hands-on experience with performing dPCR, ddPCR and/or qPCR test method execution required.

o   Experience with statistical analysis of analytical data and stability studies preferred

o   Experience with viral vectors is not required but experience with biologics preferred

o   Independently motivated and detail-oriented with good problem solving ability

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