Key ResponsibilitiesExecute end-to-end Computer System Validation (CSV) activitiesPrepare, review and approve validation deliverablesPerform risk assessments and validation planningSupport validation of SAP S/4HANA, TrackWise, QMS, DMS and enterprise applicationsWork on 21 CFR Part 11, GxP and GAMP 5 complianceSupport change management, deviation management and validation documentationConduct periodic reviews, control maturity assessments and auditsSupport SaaS and cloud qualificationWork with Agile and Waterfall methodologiesCoordinate with business, IT, QA and project stakeholdersWhat We’re Looking For4–14 years of relevant Life Sciences / Pharmaceutical experienceStrong hands-on CSV / IT Validation experienceGood knowledge of GAMP 5, 21 CFR Part 11 and GxPExperience with regulated enterprise applicationsStrong documentation and validation lifecycle knowledgeExposure to SaaS / Cloud validation is an advantageStrong communication and stakeholder management skillsIT / Computer Science / Engineering background preferredWe are looking for experienced Computer System Validation (CSV) / IT Validation professionals to join our Life Sciences practice and support pharmaceutical clients across validation, compliance and digital transformation initiatives.Interested candidates can share their updated resume with passport pics attached at: csv.staffing@mazars.co.in and Harshita.sengar@mazars.co.in - mark all of them with your profile summary (Linkedin ID Link) along with details of their notice period and current location, CTC (Fixed + Variable) & Expected CTC

CSV / IT Validation Professional for Life Sciences (4–14 Years)

Emma

Responsibilities

Skills wanted:

Language(s) required:

Pooja Gupta

Pooja Gupta

About Forvis Mazars:

www.forvismazars.com/group/en

Admin access needed