The Technical Writer will support pharmaceutical validation activities by preparing, reviewing, and maintaining high‑quality validation documentation in compliance with GMP, data integrity, and regulatory requirements. The role focuses on Kneat‑based documentation, protocol preparation, execution review, and summary reporting. ResponsibilitiesDocumentation & WritingDraft, edit, and finalize validation protocols, execution summaries, and final reports using Kneat softwarePrepare structured documentation such as IQ/OQ/PQ summaries, qualification reports, and validation deliverablesEnsure documentation follows Good Documentation Practices (GDP) and site‑specific SOPsReview & ComplianceReview Kneat execution entries for accuracy, completeness, and complianceSupport pre‑ and post‑execution documentation reviewsEnsure all validation documents meet regulatory requirements (e.g. GMP, data integrity, audit readiness)Collaboration & SupportWork closely with Validation Engineers, QA, and Project Teams to ensure documentation aligns with executed activitiesTrack documentation status, revisions, and approvalsSupport audit and inspection readiness through well‑maintained documentationQualificationsDiploma or Degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related fieldHands‑on experience with Kneat documentation systemExperience writing or supporting validation protocols and reportsStrong understanding of GMP and Good Documentation Practices (GDP)Familiarity with validation lifecycle documentation