Document Control Specialist

2 weeks ago


Austin, United States GForce Life Sciences Full time

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


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