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Document Control Specialist

GForce Life Sciences
Austin, TX, United States
Temporary

Job Details :

Internal Job Title : QA Specialist II

Duration : 6-month contract

Location : Onsite - Austin, TX

Special Notes : Will start with the standard Monday - Friday shift for training, and will then move to Wednesday - Saturday shift

Responsibilities :

  • This person will ensure the quality of manufactured products and processes per standard operating processes (SOP) and GMP (Good Manufacturing Practices).
  • DHR review - review batch records for med device
  • This role will be primarily in a desk environment

Qualifications :

  • Bachelor's Degree in a related field
  • 0-2 years of previous experience
  • Previous experience with document review in the pharma / med device industry
  • Strong understanding of Medical Device Quality Documents
  • 30+ days ago
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