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# USA - Technical Writer II (IT) (contract)

- **Company:** Sanofi
- **Location:** Swiftwater, PA, United States
- **Salary:** $112,320.0
- **Contract:** Temporary to permanent
- **Skills:** Laboratory Information Management Systems, Data Management, Veeva
- **Published:** June 5, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=2efcc54e4ef01667

## About the Role

Do you have experience in User training (technical support)?, Do you have a Bachelor's degree?, * 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.

## Description

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., * 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


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