Quality Systems Technical Writer and Documentation Specialist
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:
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BioPharm Systems, Inc.

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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