Overview
Technical Writer Med / Clin I in the Operations Labeling Group. You will be responsible for creating, revising, and maintaining high-quality labeling documents for our medical products.
Key Responsibilities
- Develop and maintain labeling instructions for use / Method Sheets (IFU / MS)
- Ensure labeling content is accurate, clear, and consistent with regulatory and company global standards
- Review and edit labeling documents to ensure clarity, consistency, and compliance
- Coordinate labeling activities to ensure timely completion of projects
Qualifications
Bachelor\'s degree in Technical Writing, Communications, Life Sciences, or related fieldMinimum of 3 years experience as a technical writer, preferably within the pharmaceutical, biotechnology, or medical device industryFamiliarity with regulatory requirements and guidelines for medical product labeling (e.g., FDA, EMA, etc.)Excellent writing, editing, and proofreading skillsStrong attention to detail and ability to manage multiple projects simultaneouslyProficient in using document management systems and authoring tools such as Adobe Acrobat, Microsoft Office, etc.Ability to work independently as well as collaboratively in a team environmentStrong organizational and time management skillsEffective communication skills and ability to convey complex information clearlyPreferred Qualifications
Experience with component content management systems (CCMS)Experience with labeling system softwareJob Details
Industry : Medical DevicesTitle : Technical Writer Med / Clin IJob ID : ROCGJP00037578Location : Branchburg, NJDuration : 12 months contract (High Chances of Extension)Compensation
Base pay range : $45.00 / hr - $54.00 / hr
Direct message the job poster from TalentBurst, an Inc 5000 company
About the role : As a Technical Writer in the Operations Labeling Group, you will be responsible for creating, revising, and maintaining high-quality labeling documents for our cutting-edge medical products.
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