Technical Writer Job

Needed: Technical Writer– Pharma (Hybrid – New Brunswick, NJ)

We are seeking a Technical Writer – Pharma for our global pharmaceutical client. You will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). The focus of the role is to deliver CMC documentation (dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application. This role requires effective collaboration across technical functions to deliver on timelines for submissions. The position interfaces with experts in Process Development, Analytical Development, Cell Therapy Technical Ops, Quality and Regulatory Sciences across CTDO.

This is a 40-hour per-week, 12-month contract (extensions possible), 50% onsite at the client’s office in New Brunswick, NJ. Work Schedule: Mon-Fri (normal business hours). Travel occasionally to other local NJ sites for larger team meetings (2-3 times a year)

This is a W2 role as a Stage 4 Solutions employee. Health benefits and a 401K are offered.

To learn more and to apply, please go to: https://hubs.la/Q03KKjPm0 (Please apply to the Technical Writer– Pharma (Hybrid – New Brunswick, NJ)) role.

Please feel free to forward this project opening to others who may be interested.

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