Are you an experienced Technical Author looking to join a leading company in the healthcare and pharmaceutical sectors? This company, a pioneer in manufacturing clean air and containment equipment, is seeking a dedicated Technical Author to contribute to their innovative team in Heywood. This is an exceptional opportunity to be part of a dynamic organization that values precision, collaboration, and continuous improvement. The ideal candidate should have a degree or equivalent compliance experience in a similar industry, with desirable knowledge of medical and pharmaceutical validation. The role requires experience in validation protocols, risk assessments, and operator manuals, alongside an understanding of CE and UKCA compliance and related directives Key Responsibilities of the Technical Author - Produce high-quality validation, compliance, and technical documentation to support the design and manufacture of the company's products. - Prepare essential validation documentation including Requirements Traceability Matrices, Design Qualifications, Factory Acceptance Tests, Installation and Operation Qualifications, Operator Manuals, and Risk Assessment and Method Statements. - Develop Standard Test Protocols and procedure manuals, ensuring adherence to applicable protocols, guidelines, and legal standards. - Collaborate closely with the Compliance Engineer and other departments such as Production, Customer Care, Sales, and After...