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Quality Systems Technical Writer and Documentation Specialist

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Company/Organization: BioPharm Systems, Inc.

Description:

Under the direction of the Director of QA:
- Author internal audit plans and summary reports
- Assist in the follow up of internal audit findings to ensure remediation of observations
- Assist with storing and archiving controlled documents
- Assist in sending controlled document effectivity notifications, training notifications, updating the staff training matrix, tracking completion of training, and initiating CAPAs for employee training records
- Perform administrative tasks
- Assist with on-boarding and termination activities
Assist with internal auditing of:
- Change control records
- Deviations and corrective and preventative actions (CAPAs)
- Employee training records, resumes, and job descriptions
- Application Support tickets
- Periodic review of POL, SOPs, GDL, FRM, and REF documents
- Software inventory and GxP assessments
- Project or process deliverables

Qualifications:

- 4 year degree completed or in progress
- Expertise with Microsoft Office including Word, Visio, and Excel
- Strong writing skills
- Strong problem-solving abilities
- Detail oriented

Hours:

20 hours a week

Length/Availability:

Flexible

End Date:

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Tags:
QA  IT  PAID  INTERNSHIP  PART-TIME 
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BioPharm Systems, Inc.

See http://www.biopharm.com/
BioPharm Systems, Inc.    [ All of our Internships ]

2000 Alameda de las Pulgas, Suite 154
San Mateo, CA 94403

Phone: 650-292-5332
Email:  rgavan@biopharm.com
Website:  BioPharm Systems, Inc.

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