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.