{"id":3510154,"url":"https://alion.io/job/centrient-pharmaceuticals-global-it-qa","title":"Global IT QA","company":{"id":673573,"name":"Centrient Pharmaceuticals","domain":"centrient.com","url":"https://alion.io/company/centrient","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workable","truth_index":{"grade":"A","score":86,"open_postings":9,"ghost_share":0,"stale_share":0.556,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-11-01T06:10:25Z"}},"role":"Marketing","role_family":"Marketing","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":["Gurgaon, India"],"countries":["IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"21 CFR Part 11","optional":false},{"name":"CAPA","optional":false},{"name":"GMP","optional":false},{"name":"Veeva","optional":false}],"status":"live","first_seen_at":"2026-10-30T07:29:23Z","employer_posted_date":"2026-10-30","last_verified_at":"2026-11-01T07:07:10Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"Purpose of the Role:-\nReporting to the Global QA Director CSV and Data Integrity, providing governance and services to Global IT and supporting the global audit programme. Ensure global GMP applications (SAP,\nTrackwise, Master Control, Veeva and Infrastructure) compliance with CSV and Data Integrity best practice according to applicable regulations and Corporate Policy and Procedure.\nWork with partners in Global IT to ensure that new projects and changes are executed to maintain the validated state.\nApply GMP & cGMP as meant by 21 CFR part 11, EU GMPs Annex 11, GAMP and current eDI best practice. Ensure embedding of Quality and Validation in the total approach, thinking and\nacting. Coach and train direct colleagues as well as Key-Users. Audit CSV and eDI for Local Sites, System Vendors, CMO, CLO and Global IT.\nKey Individual Accountabilities:-\n\nProvide QA governance to CSV and eDI practices for Global GMP systems\n\nProactively participate in Global IT projects (new systems and changes)\n\nProactively participate in Global IT quality improvement projects\n\nEnsure Change Control governance in line with processes and stakeholders such as Local site QA, IT and respective\nBusiness Owners\n\nActs as System Subject Matter Expert on systems Quality and Validation\n\nOrganize trainings on CSQ processes\n\nDefine and maintain the GMP compliancy audit agenda for the Centrient sites and business units and Qualified Vendors.\nKey Shared Accountabilities :-\n. Participate in relevant teams for all CSQ and core business process projects to ensure that the necessary validation activities are identified and carried out\n\nParticipate and provide leadership and technical SME to Global CSV and DI improvement projects\n\nParticipate in Corporate Audit (Virtual and On site) and for Computerized System\n\nProvide IT CSV support for agency audits including multiple international agencies at one time.\nKey Leadership behaviors:-\n\nCommunicates effectively with a diverse audience\n\nAbility to lead and manage project teams\n\nGreat team player\n\nFast learner\n\nOpen and value / result oriented\n\nIntercultural skills\nOwns & Influences\nCompliance of Global IT systems to applicable\nregulation\n\nExternal inspection & audit support\n\nAudit planning, execution, reporting and monitoring\nEstablish a computer system validation framework that is clear and effective for all stakeholders involved in projects and day to day operation and maintenance\nRequirements\nRequired Competencies:-\nWorking knowledge of Global IT systems (SAP, Document Management System, CAPA Management Systems)\nStrong Quality and continuous improvement mindset\nDeep expertise in Computer System Validation and Data Integrity for the Pharmaceutical industry\nIndependent and reliable worker\nTeam player\nStrong communications skills\nIntercultural skills\nGood Knowledge of GxP Analysis, Gap Assessment, Risk Assessment.\nGood Knowledge of 21 CFR Part 11, CSV - GAMP and electronic Data Integrity\nExperience : 8yrs. to 15 yrs.\nEducation:-\nUniversity degree in technical, science, chemical engineering or computer sciences","description_format":"text","description_chars":3065,"description_truncated":false,"requirements":{"experience_years_min":null,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Generic Drugs","APIs & Drug Manufacturing"],"lifecycle":[{"event":"open","at":"2026-10-30T07:29:23Z"}],"visa":[],"liveness":{"score":86,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.86,"p_room":1,"age_days":1,"expected_fill_days":24,"reasons":["conf:2","win:early"],"computed_at":"2026-11-01T06:10:25Z"},"pay":null,"html_url":"https://alion.io/job/centrient-pharmaceuticals-global-it-qa","json_url":"https://alion.io/job/centrient-pharmaceuticals-global-it-qa.json","meta":{"generated_at":"2026-11-01T08:06:47Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":12615,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-02T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":673573},"rest":"https://alion.io/mcp/rest/get_company?id=673573"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fcentrient-pharmaceuticals-global-it-qa"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fcentrient-pharmaceuticals-global-it-qa"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fcentrient-pharmaceuticals-global-it-qa"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/centrient-pharmaceuticals-global-it-qa\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fcentrient-pharmaceuticals-global-it-qa"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3510154}},{"tool":"search_jobs","arguments":{"company":"centrient.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3510154},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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