QC Associate I

South San Francisco, California | Contract

Post Date: 01/08/2018 Job ID: 3736 Industry: Quality and Regulatory Affairs

Our client is a leading biotechnology company that discovers, develops, manufactures and commercializes medicines to treat patients with serious or life-threatening medical conditions. They  are among the world' s leading biotech companies, with multiple products on the market and a promising development pipeline.

 

Duties: 
  • Support method development and validation.
  • Execute, author and/or review protocols, data summaries, report and project binders.
  • Assist in QC investigation as needed.
  • Troubleshoot method and instrumentation problem as needed
  • Complete or provide cross-training and training as required on procedures and analytical methods
  • Maintain GMP compliance
  • Ensure laboratory areas and data are inspection ready at all times
  • Monitor and report all safety events and near-miss events observed per standard safety procedures and work with
  • EHS as required.
  • Mitigate and prevent ergonomic-related injuries

 

 

Skills:

  • BS in Chemistry, Biochemistry, Analytical Chemistry, Chemical Engineering, or other related degree concentration
  • At least 2 year analytical chemistry experience
  • Must be able to independently run well-defined experiments and analyze and/or review data
  • Knowledge of regulatory guideline and industry standards, including cGMP

 

Education:

  • BS in Chemistry, Biochemistry, Analytical Chemistry, Chemical Engineering, or other related degree concentration
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