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Documentation Specialist I
Ref No.: 20-05067
Location: Hillsboro, Oregon

The successful candidate will be responsible for issuance of production documents. Duties include but not limited to printing and issuance of GMP documents. They are also responsible for effectively following SOPs, policies, and cGMPs. Adhere to and enforce Genentech policies and procedures related to document control. Attend cGMP training per department policy. Complete SOP and on-the job training per department policy.

  • Must have ability to take initiative and work with little supervision.
  • High level of professionalism and the ability to interact with personnel at all levels.
  • High degree of skill and comfort with computer applications.
  • Demonstrate ability to work accurately, follow instructions, and handle multiple priorities.
  • Very strong organizational and communication skills.
  • Knowledge of cGMP regulations and concepts preferred, particularly in good documentation practices. Experience in pharmaceutical/biotech or other GMP-regulated industry preferred.

AA/AS Degree and 1-2 years-related work experience preffered

Is this contractor working in a GMP environment?: Yes
Second Job Title: Documentation Specialist