{"id":3377485,"url":"https://alion.io/job/evotec-equipment-support-technician","title":"Equipment Support Technician","company":{"id":715207,"name":"Evotec","domain":"evotec.com","url":"https://alion.io/company/evotec-website-english","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":79,"open_postings":14,"ghost_share":0,"stale_share":0.857,"repost_share":0,"time_to_fill_p50_days":26,"computed_at":"2026-11-01T06:10:25Z"}},"role":"Support","role_family":"Support","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Verona, Italy"],"countries":["IT"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":21000,"max_usd":46000,"period":"year","method":"role_country_seniority_unknown","sample_n":50},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"GMP","optional":false},{"name":"Mass Spectrometry","optional":false}],"status":"live","first_seen_at":"2026-10-27T00:00:00Z","employer_posted_date":"2026-10-27","last_verified_at":"2026-11-01T13:22:32Z","board_verified":true,"closed_at":null,"days_open":5,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":5},"description":"DUTIES AND RESPONSIBILITIES\nRegulatory / Compliance\nMaintain a thorough understanding of applicable SOPs, cGMP requirements, and company policies relevant to assigned activities.\nEnsure full compliance with the Quality Management System and regulatory requirements within Pharmaceutical Sciences, Aptuit Verona.\nPerform all activities in accordance with site safety procedures and guidelines.\nAuthor, review, and maintain Standard Operating Procedures (SOPs) and related documentation.\nManage equipment-related deviations, investigations, CAPAs, and Change Controls, ensuring timely completion and effectiveness.\nSupport the implementation and follow-up of corrective and preventive actions.\nMaintain training records up to date and complete all required training activities in a timely manner.\nTechnical / Scientific\nSupport the qualification, maintenance, calibration, administration, and lifecycle management of laboratory equipment and computerized systems.\nDefine business requirements and provide technical expertise for equipment qualification, maintenance, and performance monitoring activities.\nCoordinate and manage third-party suppliers involved in equipment maintenance, qualification, and laboratory support services.\nDevelop and support business continuity plans for critical laboratory equipment and processes.\nPlan, execute, review, and document qualification, requalification, and maintenance activities.\nAuthor and review qualification protocols, reports, risk assessments, and technical documentation.\nEnsure maintenance schedules are effectively managed and completed according to plan.\nTroubleshoot equipment and configuration issues, providing timely user support to minimize laboratory downtime.\nInvestigate equipment incidents, identify root causes, assess operational impact, and support implementation of corrective actions.\nDefine and oversee GMP requirements related to laboratory instrumentation and computerized systems.\nManage the lifecycle of SOPs and controlled documents related to equipment management.\nSupport internal audits, client audits, and regulatory inspections, acting as a subject matter expert for equipment-related topics.\nAdministrative / General\nFoster clear and effective communication with colleagues, stakeholders, and management.\nKeep the supervisor informed of progress, priorities, issues, and achievements.\nCollaborate effectively within cross-functional teams and contribute positively to team objectives.\nDemonstrate flexibility and adaptability in managing changing priorities and workloads.\nExhibit strong organizational and planning skills to ensure efficient execution of assigned activities.\nApply sound problem-solving and decision-making skills to resolve technical and operational issues.\nPromote a culture of continuous improvement, compliance, and operational excellence.\nRequirements:\nExperience with GC-MS, LC-MS systems and laboratory equipment used for physical analysis and characterization is considered an advantage.\nWorking experience in GMP environment.\nEnglish minimum low-intermediate English\nFR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.\nEN: In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.\nIT: In compliance with fundamental ethical and professional principles and with Legislative Decree 198/2006, Evotec is an Equal Opportunity Employer committed to fostering a safe, diverse, and inclusive workplace built on mutual respect. We provide equal employment opportunities to all qualified candidates and employees based on their skills, experience, and professional qualifications. In line with our ethical and professional principles, all employment-related decisions, including recruitment and selection processes, are made fairly and without any form of discrimination. 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