What are the responsibilities and job description for the Technical Writer Med/Clin I position at Compass Consulting?
About the Company: Our client develops, manufactures and supplies a wide array of innovative medical diagnostic products, services, tests, platforms and technologies.
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.
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:
- Bachelors 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 Skills:
- Experience with component content management systems (CCMS).
- Experience with labeling system software.
Please note this opportunity is not eligible for C2C.
