{"id":3002229,"url":"https://alion.io/job/medpharm-computer-system-validation-specialist-csv-medpharm","title":"Computer System Validation Specialist (CSV) - MedPharm","company":{"id":2322662,"name":"MedPharm","domain":"medpharm.com","url":"https://alion.io/company/medpharm-com","size_band":"51-200","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"JazzHR","truth_index":null},"role":"Biotech","role_family":"Biotech","seniority":"middle","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Guildford, United Kingdom"],"countries":["GB"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":53000,"max_usd":128000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":136},"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"21 CFR Part 11","optional":false},{"name":"GLP","optional":false},{"name":"GMP","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-10-21T12:35:14Z","employer_posted_date":"2026-10-21","last_verified_at":"2026-10-28T00:05:17Z","board_verified":true,"closed_at":null,"days_open":6,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":6},"description":"Position Summary\nThe Computer System Validation (CSV) Specialist is responsible for the governance, validation, and lifecycle management of all GxP-relevant computerised systems at site.\nThis role ensures ongoing compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, GAMP5 principles, and applicable global regulatory requirements. The position provides technical oversight of electronic systems, manages validation activities, assesses system updates and changes, and closes existing CSV compliance gaps to maintain inspection readiness and data integrity.\nEssential Functions\nOwn and maintain the site Computerised Systems Validation (CSV) Master Plan.\nManage the full validation lifecycle of GxP systems (URS, risk assessment, IQ/OQ/PQ, validation reports).\nAssess and approve system updates, configuration changes, and upgrades in line with change control procedures.\nConduct risk-based impact assessments for system changes and new implementations.\nPerform and document periodic system reviews to ensure ongoing validated state.\nIdentify and close existing CSV gaps to ensure compliance with Annex 11 and data integrity requirements.EudraLex Volume 4 Good Manufacturing Practice (GMP) guidelines, laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/EEC respectively\nUK Good Laboratory Practice Regulations 1999, Statutory Instrument No. 3106 as amended by Statutory Instrument 2004/994 \nOECD Series on Principles of Good Laboratory Practice and Compliance Monitoring No1 \nOECD Principles of Good Laboratory Practice ENV/MC/CHEM(98)17 \nOECD Series on Principles of Good Laboratory Practice and Compliance Monitoring Nos. 2-25 \nMHRA ‘GxP’ Data Integrity Guidance and Definitions March 2018\nUS 21 CFR Part 11\nUS 21 CFR Part 210 & 211 (US GMPs)\n• Ensure appropriate audit trail review processes are defined and implemented.\nSupport supplier qualification and oversight of SaaS/cloud-based system providers.\nProvide inspection support for MHRA and other regulatory authorities.\nCollaborate with QA, IT, Operations, and external vendors to ensure compliant system management.\nDevelop and maintain CSV templates, procedures, and best practices aligned with GAMP5 principles.\nStandard bullet list item for all people manager positions:\nAttracts, develops, and retains a high performing team to meet the current and evolving needs of the business through effective selection, training and development, coaching and mentoring and performance management.\n Education and ExperienceBachelor’s degree in Life Sciences, Pharmacy, Engineering, Computer Science, or a related scientific discipline (or equivalent relevant experience).\nMinimum 3-5 years’ experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical, biotechnology, or clinical research environment.\nDemonstrated hands-on experience with MasterControl (or equivalent eQMS), including configuration assessment, validation, and lifecycle management.\nPractical experience validating GxP computerised systems in accordance with EU GMP Annex 11 and GAMP5.\nExperience conducting system risk assessments, change impact assessments, and periodic reviews.\nExperience supporting regulatory inspections (e.g., MHRA, FDA) relating to computerised systems and data integrity.\n Knowledge, Skills, and AbilitiesStrong knowledge of EU GMP Annex 11 requirements.\nGood understanding of MHRA Data Integrity Guidance and ALCOA+ principles.\nKnowledge of GAMP5 risk-based validation methodology.\nUnderstanding of 21 CFR Part 11 (where applicable).\nKnowledge of computerised system lifecycle management in a regulated environment.\nAbility to prepare and review validation documentation (URS, IQ/OQ/PQ, validation reports).\nStrong analytical and risk assessment skills.\nAbility to assess system changes and determine validation impact.\nStrong written and verbal communication skills.\nAbility to manage multiple validation projects and priorities simultaneously.\nEffective cross-functional collaboration skills (QA, IT, Operations, external vendors).\nProficiency with Microsoft Office (Word, Excel, PowerPoint, Teams, etc.) required.\nTravel RequirementsNone \nPhysical Demands and Work EnvironmentThe physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.\nWhile performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is occasionally required to walk; sit; climb or balance and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.\nOther Duties\nPlease note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.\nLimitations and Disclaimer\nThe above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. All job requirements are subject to possible modification to reasonably accommodate individuals with disabilities. This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow job-related instructions and to perform other job-related duties requested by their supervisor in compliance with Federal and State Laws. Requirements are representative of minimum levels of knowledge, skills, and/or abilities. 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