Documentation Specialist
- Employer
- Ware Technology Services
- Location
- Minneapolis, MN
- Start date
- Aug 2, 2019
- Closing date
- Sep 1, 2019
View more
- Category
- Healthcare
- Job Type
- Employee
- Employment Status
- Full Time
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Job Details
Ware Technology Services is recruiting for a Direct Hire Documentation Specialist!
The Document Control Specialist reports directly to the Director of Quality. The Document Control Specialist supports quality assurance activities by reviewing records and documents for accuracy, completeness and adherence to the company quality management system, customer requirements, and cGMP regulatory requirements. The Document Control Specialist performs document management and administrative support tasks for SOP and batch record systems as well as other tasks to assure the schedules and goals of the quality system are met. Perform QA document control functions, including document logs, tracking, processing, review, distribution, release, scanning, and archiving of documents
Coordinate the revision, review, and approval and retirement of SOPs and other GMP documents
Organize and ensure accurate and reliable filing systems for all paper-based GMP documents
Quality professional with a minimum of 2-3 years of hands on experience performing document management in a regulated pharmaceutical or medical device industry with direct document control experience
Demonstrated knowledge of cGMPs, 21 CFR 210, 211, and 820 and other regulatory agency requirements sufficient to apply to quality operations and compliance
Must be skilled in the use of MS office applications such as Word, Excel, PowerPoint and Adobe Acrobat
The Document Control Specialist reports directly to the Director of Quality. The Document Control Specialist supports quality assurance activities by reviewing records and documents for accuracy, completeness and adherence to the company quality management system, customer requirements, and cGMP regulatory requirements. The Document Control Specialist performs document management and administrative support tasks for SOP and batch record systems as well as other tasks to assure the schedules and goals of the quality system are met. Perform QA document control functions, including document logs, tracking, processing, review, distribution, release, scanning, and archiving of documents
Coordinate the revision, review, and approval and retirement of SOPs and other GMP documents
Organize and ensure accurate and reliable filing systems for all paper-based GMP documents
Quality professional with a minimum of 2-3 years of hands on experience performing document management in a regulated pharmaceutical or medical device industry with direct document control experience
Demonstrated knowledge of cGMPs, 21 CFR 210, 211, and 820 and other regulatory agency requirements sufficient to apply to quality operations and compliance
Must be skilled in the use of MS office applications such as Word, Excel, PowerPoint and Adobe Acrobat
Company
Engineering & IT
As in any profession, the key to success is knowing what your strengths are and then finding the opportunity to use them. Ware Technology Services allows you to utilize and develop your skills through exciting projects with great companies in your area. And, because we take care of all the work involved in finding the right opportunities, you can focus on advancing your career.
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