Technical writing with labelling & Pharma
Dawar Consulting
Job Description
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
If interested, please send us your updated resume at View email address on click.appcast.io/View email address on click.appcast.io
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.
- 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.
If interested, please send us your updated resume at View email address on click.appcast.io/View email address on click.appcast.io
Vacancy posted 4 days ago
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