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Qa Document Specialist Jobs
Company | ZEISS Group |
Address | , Chesterfield, Mo |
Employment type | FULL_TIME |
Salary | |
Expires | 2023-07-15 |
Posted at | 1 year ago |
As a Quality Assurance Document Specialist, you will:
- Help review document changes helping to determine possible impact to regulatory and operational compliance
- Help monitor Quality Assurance logs and tasks and help to push the projects or documents to completion
- Document review observations such as suggested edits/comments, if applicable
- Review and approve non-DMS documents (QA Monthly Preventative Maintenance, Engineering Preventative Maintenance documents, Calibration Records, Training Records, Customer Complaints, Nonconformances, etc.)
- Help manage documentation overhaul projects
- Identify and implement improvements to established processes, by working closely with engineering and regulatory personnel
As a Quality Assurance Document Specialist, you bring to the table:
- Strong communication skills, both written and spoken
- Ability to multi-task on different projects, while maintaining high quality performance
- Strong organizational skills
- Ability to work cross-functionally with a team, including engineering, regulatory, marketing, and manufacturing personnel
- Proficiency in Microsoft Office applications, including Word and Excel
- An Associate’s or Bachelor’s degree, preferably in a technical field of study
- Ability to problem solve and think outside of the box
- Great attention to detail, especially proofreading of documentation prior to approval
- 0-3 years experience in a relevant field
Bonus Points for the Following:
- Experience in the medical device field, or another regulated industry
- Experience with technical writing
- Experience with project management
Your ZEISS Recruiting Team:
Christina Choing-
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