QC Technical Writer (3-Month Contract)

QC Technical Writer (3-Month Contract) | GMP | OnsiteI’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 RoleThis 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:Authoring and editing analytical methods, protocols, and technical reportsSupporting documentation related to method qualification and validationReviewing and improving existing QC documentation for clarity and complianceEnsuring all documentation aligns with GMP and regulatory standardsCollaborating with QC, Analytical Development, and QA teamsSupporting documentation for technology transfer and commercial readinessWhat They’re Looking ForExperience working in a GMP-regulated environment (pharma, biotech, CDMO)Strong background in technical writing within QC or Analytical DevelopmentExperience with analytical methods, validation, or laboratory documentationExcellent written communication skills with strong attention to detailAbility to translate complex scientific data into clear, compliant documentationWhy This Role?Join a company undergoing significant GMP expansion and commercial growthHigh-impact role supporting QC and analytical readiness for manufacturingWork closely with scientific teams in a highly collaborative environmentFast-moving process with immediate start availableStrong potential for extension beyond the initial 3-month contractIf this sounds interesting, feel free to apply or message George Higginson directly for a confidential discussion.