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Technical Writer

Greenville, NC💼 Full-time🗓 2026-07-10 → 2026-07-30

Core

Creating, organizing, and formatting technical documentation (Master Batch Records, protocols) for manufacturing and packaging operations.

Role type

Technical Writer (Manufacturing/Pharma)

Builds

Manufacturing documentation and change control records

Domain

Pharmaceutical manufacturing / Oral solid dosage forms

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Technical writing, GMP documentation knowledge, database management, Microsoft Office (Word, Excel), Adobe Professional

Preferred skills

Quality system administration, electronic document software implementation

Responsibilities

Gather information from SMEs to create or update documents, review documents for accuracy and consistency, input data into inventory and Manufacturing Resource Planning systems, close out help desk tickets for document corrections, provide information during client and FDA audits, coordinate document approval across the organization

Seniority

Entry-level to Mid-level

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