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Job Requirements of Technical Writer:
-
Employment Type:
Full-Time
-
Location:
Branchburg, NJ (Onsite)
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Technical Writer
Tailored Management Services Inc
Branchburg, NJ (Onsite)
Full-Time
Job Title: Technical Writer
Location: 1080 US Highway 202 South, Branchburg, NJ 08876
Duration: 12+ Month Contract (Potential for Extension or Conversion to Permanent)
Pay Rate: $25.05 – $52.76/hr (W2)
Benefits: Weekly Pay, Vision, Dental, and Medical Coverage
About the Role
We are seeking a skilled Technical Writer to join the Operations Labeling Group. In this role, you will be responsible for developing, revising, and maintaining high-quality labeling documents that support our innovative medical products. You will play a key part in ensuring that labeling materials are accurate, compliant, and user-friendly for a global audience.
Key Responsibilities
Required Qualifications
Preferred Qualifications
Location: 1080 US Highway 202 South, Branchburg, NJ 08876
Duration: 12+ Month Contract (Potential for Extension or Conversion to Permanent)
Pay Rate: $25.05 – $52.76/hr (W2)
Benefits: Weekly Pay, Vision, Dental, and Medical Coverage
About the Role
We are seeking a skilled Technical Writer to join the Operations Labeling Group. In this role, you will be responsible for developing, revising, and maintaining high-quality labeling documents that support our innovative medical products. You will play a key part in ensuring that labeling materials are accurate, compliant, and user-friendly for a global audience.
Key Responsibilities
- Create, revise, and maintain Instructions for Use (IFU) and Method Sheets (MS).
- Ensure all labeling content is accurate, clear, and compliant with regulatory requirements and Roche global standards.
- Review and edit labeling documents for clarity, consistency, and compliance.
- Collaborate cross-functionally to coordinate labeling activities and deliverables.
- Manage multiple projects simultaneously, meeting deadlines without compromising quality.
Required Qualifications
- Bachelor’s degree in Technical Writing, Communications, Life Sciences, or a related field.
- 3+ years of experience as a Technical Writer, ideally within pharmaceuticals, biotechnology, or medical devices.
- Strong understanding of regulatory requirements for medical product labeling (e.g., FDA, EMA).
- Exceptional writing, editing, and proofreading skills with attention to detail.
- Proficiency with document management systems and tools such as Adobe Acrobat and Microsoft Office Suite.
- Ability to work independently and collaboratively in a fast-paced, team-oriented environment.
- Excellent time management and communication skills to clearly convey complex information.
Preferred Qualifications
- Experience with component content management systems (CCMS).
- Familiarity with labeling system software and related workflows.
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