Our client, a world leader in diagnostics and life sciences, is looking for a
"
Technical Writer
"
based out of
Branchburg, NJ

Job Duration:

Long Term Contract (Possibility Of Further Extension)

Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

As a Technical Writer in the Operations Labeling Group at Roche, you will be responsible for creating, revising, and maintaining high-quality labeling documents for medical products. You will ensure all content meets regulatory requirements, global standards, and company guidelines while supporting the timely completion of labeling projects.

Key Responsibilities

• 
  Develop and maintain labeling documents, including Instructions for Use (IFU) and Method Sheets (MS).
• 
  Ensure labeling content is accurate, clear, consistent, and compliant with regulatory and company standards.
• 
  Review, edit, and proofread labeling documents to ensure quality and compliance.
• 
  Collaborate with cross-functional teams to coordinate labeling activities and meet project timelines.
• 
  Manage multiple labeling projects simultaneously, ensuring timely completion.

Requirements

• 
  Bachelor’s degree in Technical Writing, Communications, Life Sciences, or a related field.
• 
  Minimum of 3 years of experience as a Technical Writer, preferably in the pharmaceutical, biotechnology, or medical device industry.
• 
  Strong knowledge of regulatory requirements and guidelines for medical product labeling (e.g., FDA, EMA).
• 
  Excellent writing, editing, and proofreading skills with strong attention to detail.
• 
  Proficiency with document management systems and authoring tools (e.g., Adobe Acrobat, Microsoft Office).
• 
  Ability to work independently and collaboratively in a team environment.
• 
  Effective communication skills with the ability to convey complex information clearly.

• 
  Experience working with Component Content Management Systems (CCMS).
• 
  Familiarity with labeling system software.

hr@dawarconsulting.com
/kavitha
@dawarconsulting.com