Job Description

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.

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