QC Technical Writer (3-Month Contract) | GMP | Onsite
I’m currently partnered with a biologics-focused CDMO who are continuing to scale their GMP operations as they move towards commercial readiness across the US. As part of this growth, they are looking to bring on a QC Technical Writer on an initial 3-month contract , with strong likelihood of extension.
The Role
This position will focus on supporting the QC and Analytical teams with technical documentation , ensuring all methods, protocols, and reports are clearly written, compliant, and inspection-ready. You’ll play a key role in bridging science and documentation , working closely with QC, Analytical Development, and QA teams.
Key responsibilities include:
What They’re Looking For
Why This Role?
If this sounds interesting, feel free to apply or message George Higginson directly for a confidential discussion.
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