Documentation Specialist Job

DOCUMENTATION SPECIALIST needed for a contract opportunity with Yoh's client located in Hillsboro, OR

The Big Picture - Top Skills You Should Possess:
- cGMP
- GMP-regulated industry

What You'll Be Doing:
- The successful candidate will be responsible for scanning GMP documents using FileNet.
- Other duties include shelving documents and labeling QA file room contents, performing document audits, and generating reports at requested intervals.
- Effectively follow 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.

What You Need to Bring to the Table:
- 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

Bonus Points! Otherwise Known As Preferred Qualifications:
- Knowledge of cGMP regulations and concepts preferred, particularly in good documentation practices.
- Experience in pharmaceutical/biotech or other GMP-regulated industry preferred.
- Candidates must have at least AA/AS Degree and one to two (1 - 2) years-related work experience.

RECRUITER: Mary Nguyen

Yoh, a DayJ2W: SCIENTIFIC

MONJOB J2WPACNW

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SFSF: LS