Company DescriptionMilestone, a division of the global PM Group, provides advanced automation and digital systems consultancy services, specializing in Life Sciences and FMCG sectors. With a team of over 160 experts, we bring a comprehensive perspective to project implementation through our experience as end users, engineering consultants, and system integrators. Our service offerings include digital factory delivery, system integration, compliance, and manufacturing intelligence among others, ensuring tailored solutions for business needs. As part of the employee-owned PM Group, which operates in Europe, the UK, USA, and Asia, Milestone combines decades of expertise with a commitment to optimizing client outcomes.We are seeking an experiencedTechnical Writerto support a pharmaceutical client on a project within a start-up manufacturing facility. The successful candidate will have strongMES (Manufacturing Execution System) documentation experienceand a solid understanding of GMP environments.Key Responsibilities:Author, review, and update GMP documentation including SOPs, work instructions, and MES-related documentsSupport deviations, change controls, and CAPAs, ensuring accurate and compliant documentationCollaborate with Quality, Manufacturing, and MES teams to ensure documentation aligns with site and regulatory requirementsSupport documentation readiness for audits and inspectionsEnsure documentation reflects start-up facility processes and evolving systemsRequirements:3+ years' experience in a Technical Writing role within the pharmaceutical or biotech industryStrong experience with MES documentation in a GMP-regulated environmentProven experience authoring SOPs, and supporting deviations and change controlsExperience working in a start-up or greenfield facility is highly desirableKnowledge of EU GMP and regulatory standardsExcellent written communication and stakeholder engagement skills