Sr. Tax Analyst |
| AGA Medical Corporation, a medical technology company, is dedicated to the development, design, ... |
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Regulatory Affairs Manager |
| AGA Medical Corporation, a medical technology company, is dedicated to the development, design, ... |
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Clinical Research Associate II |
| AGA Medical Corporation, a medical technology company, is dedicated to the development, design, ... |
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Sr. Manufacturing Engineer |
| AGA Medical Corporation, a medical technology company, is dedicated to the development, design, ... |
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Financial Pricing Analyst - Job ID #6221 |
| Working at Express Scripts says something about your commitment to quality, your integrity, and ... |
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Research Associate - Molecular Biology - RA/88MON |
| WHO WE ARE
R&D Systems, Inc. is a specialty manufacturer of biological products. We ... |
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Product Quality Assurance Manager |
| AGA Medical Corporation, a medical technology company, is dedicated to the development, design, ... |
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IT Project Manager |
| Working at Express Scripts says something about your commitment to quality, your integrity, and ... |
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Chemistry Lab Technician |
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Technical Writer, Sr.
| Details |
Country: USA
Location: Minnesota-Minneapolis Plymouth, MN 55442
Total applied: 39 |
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Technical Writer, Sr.
AGA Medical Corporation, a medical technology company, is dedicated to the development, design, manufacture, and marketing of nitinol-based occlusion devices and accessories for the minimally invasive treatment of cardiovascular defects and peripheral vascular disease.As a Technical Writer, Sr., you will provide coordination and technical writing support for technical communication label and instruction for use (IFU) process. Manage label/IFU process to ensure output meets internal, US and International requirements and standards. Coordinate actions and activities relative to label and IFU process. Develop and maintain content for product labels and IFU’s. Manage translations of labels and IFU’s. Work with product development teams on developing labeling and IFU content. Release controlled documents with documented processes. Perform other similar duties as assigned. Qualifications: Bachelor in Technical Writing/Communication or equivalent preferred. Preferred work experience of 1-3 years in a medical device company with a minimum of 5 years of technical writing. Knowledge of documentation control systems/processes. Knowledge and application of ISO 13485 and other applicable international regulations. Ability to interact effectively with a cross-functional team. Computer efficiency in Framemaker, Adobe, Quark, MS Word, Excel,. Expertise in other word processing programs is preferred. Ability to constructively interact with a range of personalities and many levels of the organization. Infrequent lifting of up to 40 pounds. -For quick consideration apply here We offer an excellent compensation and benefits package including medical, dental, life insurance, disability, 401(k), and much more. An Equal Opportunity/ Affirmative Action Employer Please, No Agencies Position Information Location: Plymouth, MN Job Category: Other Contact Information reference code: 1105
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