Quality Specialist Document Control
Location: San Jose California
Description: R&D Partners is hiring Quality Specialist Document Control right now, this position will be placed in California. More details about this position opportunity please read the description below. Job Description Summary:
Responsible for assuring that quality and clinical documents and records are processed and controlled according to company approved procedures.
! Position Responsibilities and Authorities:
Document Control
- Process (review, track, copy, scan, file, archive and maintain) quality documents and records in electronic and hardcopy format per relevant procedures.
- Process change control orders.
- Review, track, file and maintain employee training records.
- Control engineering lab notebook distribution and retrieval.
- Identify and implement improvements to the document control system.
- Train personnel regarding document format, content, use, control, and the document control system.
- Audit quality records (e.g. device history records, equipment records) for completeness, accuracy, and conformance to appropriate SOP’s.
- Collect and enter data into QA databases as needed.
- Filing of quality related documents.
- Support goals and objectives
- Perform other duties as assigned.
Minimum Qu! alification, Experience & Skills Required:
Minimum five years related experience in the medical device industry. Intermediate to advanced computer proficiency (MS Word, Excel, and Outlook), excellent communication skills, time management skills, and attention to detail required. Basic knowledge of Clinical regulations and IRB processes preferred.
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If you were eligible to this position, please email us your resume, with salary requirements and a resume to R&D Partners.
If you interested on this position just click on the Apply button, you will be redirected to the official website
This position starts available on: Wed, 12 Jun 2013 15:11:02 GMT