Job Description
Have you written Technical Documents such as SOP’s? Within a Biotechnology, Pharmaceutical or Medical Device industry? We are currently seeking a Technical Writer to join a leading global Biopharma company in Westport, County Mayo, Ireland. The successful candidate will contribute to the growth of their multi-million-euro site and work within a diverse team. For a career driven Technical Writer, this role offers great progression opportunities to develop a career in Quality Assurance. Key Responsibilities: * You will assist and manage the closure of existing CAPAs and ensure robust actions are in place. * Maintain strong relationships with managers and colleagues within the technical and QA departments. * Lead and support continuous improvements projects. * Write technical documents such as SOP’s. Qualifications/Experience Required: * Previous expereince working in a similar role within a pharmaceutical, biotechnology or medical device environment. * Understanding of GMP regulations. * Knowledge of manufacturing operations. * Relevant scientific degree. * Excellent writing skills is essential