GMP Technical Writer – Onsite Documentation
Listed on 2026-09-30
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Catalent is seeking a Technical Writer to collect, organize, format, and author documents for manufacturing activities at Greenville, NC. You will input data into the site inventory system and support change controls, audits, and cross‑functional projects.
The role emphasizes GMP documentation, MS Word/Excel proficiency, and effective communication in an onsite environment. A STEM degree with experience is required.
We are seeking a motivated GMP Technical Writer – Onsite Documentation to join Catalent Pharma Solutions in SC, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP Technical Writer – Onsite Documentation role in the description above.
We appreciate your interest in this position.
Join Catalent Pharma Solutions and contribute to our ongoing work.
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