Csv , Compliance Gxp

**Req ID**: 338619 We are currently seeking a CSV, GxP to join our team in Bangalore, Karnātaka (IN-KA), India (IN). Mid-senior level test analyst, about 3-6 years Mandatory Skills: CSV, STLC Principles, GxP, 21 CFR Part 11, good written and Verbal communication skills, good knowledge of Testing tools like HPALM (TIMS), working experience in Agile...

Notice Period-Immediate Joiner or Max 10 days (Do not share long notice period profile.)Permanent Payroll - Anlage InfotechClient - NTT DATALocation - Bangalore (Hybrid- 2/3 days in a week)Role & responsibilities -Location: BengaluruExp: 5+ years (Relevant)Shift Timings: GeneralHybrid: 2 to 3 days WFOMandate Skills:** CSV, Compliance Gxp, Infrastructure...

Job Title: GxP Validation and Compliance SpecialistJob type:Full-time, ContractLocation:Hybrid (Bengaluru, Hyderabad, Delhi, Pune)About Us:Our mission at micro1 is to match the most talented people in the world with their dream jobs. If you are looking to be at the forefront of AI innovation and work with some of the fastest-growing companies in Silicon...

We are seeking a highly skilled and detail-oriented CSV Technical Writer to join our team. This role demands strong documentation capabilities, effective communication, and deep exposure to the pharmaceutical industry and CSV practices. The ideal candidate will be proficient in stakeholder management, user story writing, and technical documentation including...

Key Skills: - Application/Product development testing and experience in Computer Systems Validation (CSV)Experience in QMS, Regulatory Requirements, GxP Compliance, and Good Documentation PracticesStrictly adhereing to Business SOPs, cost & coverage, requirement specifications & formulation of Test Cases in HP ALM for the Functional, Integration, end-to-end,...

Job Description Job Description GxP Validation & Compliance Specialist (Contract) Position Type: Contract (6 Months) Open Positions: 01 Location: Bangalore (Preferred) Experience Required: 46 years Role OverviewWe are looking for a skilled GxP Validation & Compliance Specialist to ensure that all digital twin workflows comply with global regulatory...

Job Title: CSV ExecutiveLocation: BangaloreExperience: 2-4 yearsIndustry: Pharmaceutical / Biotechnology / LifesciencesKey Responsibilities:Perform validation activities for GxP computerized systems (planning, risk assessment, URS, IQ, OQ, PQ, summary reports)Prepare and review validation documentation in line with 21 CFR Part 11, EU Annex 11, and other...

Client: Mphasis Technical Skills: Mandatory Skills - 5+ years’ experience in Computer System Validation (CSV), Compliance and process. - Experience in Validation Planning, Validation Review, Validation Release - should have expertise creating Functional Requirements Specification (FRS), Validation Plan, Test Plan, IOQ. - Experience in creating IQ...

We are seeking a highly skilled and detail-oriented CSV Technical Writer to join our team. This role demands strong documentation capabilities, effective communication, and deep exposure to the pharmaceutical industry and CSV practices. The ideal candidate will be proficient in stakeholder management, user story writing, and technical documentation including...

Planning and performing of Computer Systems Validation in regulated environment. Respond CSV schedule to ensure all quality, manufacturing and engineering systems remain qualified to current GxP and GAMP5 requirements. IT systems interface Required Candidate profileWorking knowledge on US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. Develop CFR Part 11 csv...