TalentBurst, an Inc 5000 company
Software Technical Writer
TalentBurst, an Inc 5000 company, Branchburg Township, New Jersey, United States
Industry: Medical Devices
Title: Technical Writer Med/Clin I Job ID: ROCGJP00037578 Location: Branchburg NJ Duration: 12 months contract (High Chances of Extension)
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.
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. Requirements: Bachelor's degree in Technical Writing, Communications, Life Sciences, or related field. Minimum of 3 years experience as a technical writer, preferably within the pharmaceutical, biotechnology, or medical device industry. Familiarity with regulatory requirements and guidelines for medical product labeling (e.g., FDA, EMA, etc.). Excellent writing, editing, and proofreading skills. Strong attention to detail and ability to manage multiple projects simultaneously. Proficient 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 environment. Strong organizational and time management skills. Effective communication skills and ability to convey complex information clearly. Preferred Qualifications: Experience with component content management systems (CCMS) Experience with labeling system software.
Title: Technical Writer Med/Clin I Job ID: ROCGJP00037578 Location: Branchburg NJ Duration: 12 months contract (High Chances of Extension)
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.
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. Requirements: Bachelor's degree in Technical Writing, Communications, Life Sciences, or related field. Minimum of 3 years experience as a technical writer, preferably within the pharmaceutical, biotechnology, or medical device industry. Familiarity with regulatory requirements and guidelines for medical product labeling (e.g., FDA, EMA, etc.). Excellent writing, editing, and proofreading skills. Strong attention to detail and ability to manage multiple projects simultaneously. Proficient 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 environment. Strong organizational and time management skills. Effective communication skills and ability to convey complex information clearly. Preferred Qualifications: Experience with component content management systems (CCMS) Experience with labeling system software.