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Director, IT R&D Technology Platforms and Operations

Syndax Pharmaceuticals Inc. · New York, NY telecommuting permitted

Education
Master's in Pharmaceutical Science or Regulatory Affairs
Experience
36 months
Wage
Not stated
First / last seen
2026-09-26 / 2026-10-16

Experience must include

Veeva VaultGxP production systems21 CFR Part 11EU Annex 11Standard Operating ProceduresChange Management

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Where this job is advertised

National Labor Exchange (state job banks, via usnlx.com search) swa live
first seen 2026-09-26 · posted 2026-09-23

Original posting ↗

Application instructions (verbatim)

Send resumes to: zkowzic@syndax.com

This source's terms don't allow us to republish the full ad; read it at the original posting. Signed-in applicants see the full text on their fit page.

State job banks via NLx, all orders (NY, CA, TX, GA, FL) swa live
first seen 2026-09-28 · posted 2026-09-23

Original posting ↗

Application instructions (verbatim)

Send resumes to: zkowzic@syndax.com
Full posting text
Director, IT R&D Technology Platforms and Operations
Syndax Pharmaceuticals Inc. — New York, NY

Director, IT R&D Technology Platforms and Operations needed for Syndax Pharmaceuticals, Inc. located in New York, NY. Oversee the continuous operation, platform lifecycle management, role-based access administration, and operational oversight, and performance of GxP production systems with a focus on Veeva Vault and other non Veeva applications. Identify gaps and operational pain points within the GxP production systems ecosystem and translate them into prioritized enhancements that improve performance, usability, and business efficiency. Implement and enforce robust governance practices, ensuring that operational activities align with applicable requirements such as 21 CFR Part 11 and EU Annex 11 where relevant. Develop and maintain Standard Operating Procedures (SOPs), work instructions, and training materials for platform operations, validated state maintenance where applicable, data integrity controls, and regulated GxP procedures will be essential to support compliance expectations. Lead the Change Management Board, overseeing the evaluation, documentation, and approval of changes to GxP production systems, including releases, configuration updates, patches, integrations, and vendor delivered updates. 100% Telecommuting is permissible. Masters degree in Pharmaceutical Science or Regulatory Affairs and 3 years of experience performing the duties listed above. Must be willing to travel to client sites across the U.S. Send resumes to: zkowzic@syndax.com

Why we think this is a PERM ad (92% confidence): The posting names the specific employer (Syndax Pharmaceuticals Inc.) and worksite (New York, NY, with 100% telecommuting permissible), states exact minimum requirements ('Masters degree in Pharmaceutical Science or Regulatory Affairs and 3 years of experience performing the duties listed above'), and directs applicants to email a resume to a specific contact ('Send resumes to: zkowzic@syndax.com'). These are hallmark features of a PERM labor-market-test advertisement.