USA - Technical Writer II (IT) (contract)

Job Title: Technical Writer II

Location: Swiftwater, PA

Contract: 9-months (with possibility of extension)

Schedule: Monday - Friday; 8 AM - 4:30 PM

Pay Rate Max: $54 per hour

Sanofi's contingent workforce program, FLEXT Direct, is seeking a Technical Writer II for a 9-month contract.

This is an exciting opportunity to join a dynamic and fast-paced team supporting the global implementation of a critical laboratory information management system at a major pharmaceutical site. The ideal candidate will be a highly adaptable and detail-oriented professional who thrives in a high-stress environment and can quickly respond to shifting priorities. This role is central to ensuring the on-time delivery of a large-scale system implementation by producing high-quality technical documentation and supporting key project milestones in a compliant and safe manner. The successful candidate will play a vital role in maintaining regulatory compliance while collaborating closely with cross-functional teams to drive project success.

Responsibilities

• Design, develop, and update required technical documentation to support system implementation
• Assist with the editing of quality documents, including SOPs, guidelines, and validation master plans, to ensure compliance with regulatory requirements
• Create training slides and content to support end-user readiness
• Support future state process mapping efforts
• Organize, track, and plan master data review activities
• Track and manage project-specific deliverables to ensure on-time completion
• Complete all required Safety and Compliance training and associated training modules
  
  
  

Skills

• Strong verbal and written communication skills
• Excellent interpersonal and information-gathering abilities
• Ability to work effectively in a team environment and collaborate across functions
• Capacity to adapt quickly to changing priorities in a high-pressure environment
• Strong organizational and project tracking skills
• Attention to detail and commitment to regulatory compliance
  
  
  

Experience

• Prior experience working in a Good Manufacturing Practices (GMP) environment
• Prior experience with quality applications such as Veeva or LIMS
  
  
  

Qualifications

• BA/BS degree preferred
  
  
  

This role offers a unique opportunity to make a meaningful impact on a high-profile global system implementation within the pharmaceutical industry. Working at the intersection of technology, quality, and compliance, you will gain invaluable experience in a regulated environment while contributing to a project that directly supports the production of life-saving products. If you are a motivated self-starter who enjoys working on complex, large-scale initiatives alongside talented and dedicated professionals, this position offers the challenge and growth opportunity you have been looking for.