Biopharma SOPs & GDEs Technical Writer
Listed on 2026-10-27
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Quality Assurance - QA/QC
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Manufacturing / Production
Pinnaql seeks a Technical Writer to develop SOPs and Global Documents Engineering (GDE) documentation for a biopharmaceutical manufacturing environment. Draft, revise, and format documents, translating engineering requirements into clear, compliant content while ensuring consistency with GMP standards.
You will collaborate with Engineering, Manufacturing, Validation, and Quality to resolve comments and drive document reviews.
We would love to welcome a new Biopharma SOPs & GDEs Technical Writer to our organisation in United States.
As a Biopharma SOPs & GDEs Technical Writer, you will play an important part at Validation- in United States.
We invite applications for the Biopharma SOPs & GDEs Technical Writer position located in United States.
The following opportunity is for a Biopharma SOPs & GDEs Technical Writer with Validation-.
Our organisation is growing, and we are hiring a Biopharma SOPs & GDEs Technical Writer in United States.
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