Key Responsibilities:

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  Perform testing for in-process, lot release, stability studies, investigations, transfers, and validations.

  
  


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  Review assays and support technical transfer activities.

  
  


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  Write and maintain Quality Records, including Deviations, CAPA, Change Control, and test methods.

  
  


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  Participate in projects such as method transfers, new instruments, and method qualifications.

  
  


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  Use laboratory computer systems and Microsoft Office (Word, Excel, PowerPoint).

  
  


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  Utilize GMP Quality Systems such as Track...