Spec 2, Technical Writing

Saviance

$80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in technical writing for medical devices or IVD products
  • Strong understanding of regulatory requirements and compliance standards
  • Proven proofreading and editing skills
  • Familiarity with Quality Management Systems (QMS)
  • Ability to work cross-functionally with various teams
  • Excellent written and verbal communication skills

Responsibilities

  • Create and edit technical documentation for medical devices and IVD products
  • Proofread and maintain product labeling to ensure clarity and compliance
  • Control and manage documentation throughout the product lifecycle
  • Collaborate with Regulatory Affairs and Quality teams for accuracy
  • Align documentation with corporate branding and global regulatory standards
  • Coordinate with cross-functional teams including R&D, Marketing, and Operations

Benefits

  • Comprehensive health and wellness programs
  • Opportunities for professional development
  • Collaborative work environment
  • Exposure to diverse teams and projects
  • Recognition and rewards for contributions
Full Job Description
On site Bill is *** The Technical Writer / Proofreader is responsible for creating, editing, proofreading, maintaining, and controlling regulatory-compliant product labeling and technical documentation for medical device and in vitro diagnostic (IVD) products. This role ensures documentation is accurate, clear, compliant, and aligned with corporate branding, Quality Management System (QMS) requirements, and global regulatory standards.

The position works closely with Regulatory Affairs, Quality, R&D, Marketing, Manufacturing, Product Management, and Operations teams to develop high-quality customer-facing documentation and labeling throughout the product lifecycle.

On site Bill is *** The Technical Writer / Proofreader is responsible for creating, editing, proofreading, maintaining, and controlling regulatory-compliant product labeling and technical documentation for medical device and in vitro diagnostic (IVD) products. This role ensures documentation is accurate, clear, compliant, and aligned with corporate branding, Quality Management System (QMS) requirements, and global regulatory standards.

The position works closely with Regulatory Affairs, Quality, R&D, Marketing, Manufacturing, Product Management, and Operations teams to develop high-quality customer-facing documentation and labeling throughout the product lifecycle.

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