Consultant | CSV | Hyderabad | SAP | DSA LS&HC

Deloitte & Touche GmbH Wirtschaftsprüfungsgesellschaft

Hyderabad

Presencial

INR 1 800 000 - 2 400 000

Tempo integral

Há 8 dias

Uma candidatura completa num minuto

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Resumo da oferta

Deloitte & Touche GmbH Wirtschaftsprüfungsgesellschaft in Hyderabad seeks an experienced Computer System Validation (CSV) and Quality Assurance professional with 5+ years of expertise in validating GxP-regulated computerized systems within Life Sciences and Healthcare. You will lead end-to-end validation activities for enterprise applications including ERP, MRP, QMS, LIMS and cloud platforms.

Strong regulatory knowledge (GMP, 21 CFR Part 11, EU Annex 11) and hands-on validation deliverables like

Qualificações

  • 5+ years of QA/Computerized System Validation in a regulated Life Sciences/Healthcare environment.
  • Knowledge of GMP, 21 CFR Part 11, 21 CFR Part 820, EU Annex 11, etc.

Responsabilidades

  • Lead end-to-end validation activities for IT projects and system releases/upgrades.
  • Define test strategy and review test cases in accordance with test plan.
  • Support internal audits and inspections and contribute to validation deliverables.

Conhecimentos

Quality Assurance
CSV
GxP Knowledge
Regulatory Knowledge
Data Migration
Cloud Validation
IT Risk Assessments
Validation Plans
URS/FS/DS
SDLC

Formação académica

BE/BTech

Descrição da oferta de emprego

The team

Enterprise technology must do much more than keep the wheels turning; it is the engine that drives functional excellence and the enabler of innovation and long-term growth. Learn more about ET&P

Experienced Computer System Validation (CSV) and Quality Assurance professional with 5+ years of expertise in validating GxP-regulated computerized systems within the Life Sciences and Healthcare industry. Proven track record of leading end-to-end validation activities for enterprise applications including ERP, LIMS, QMS, MRP, and cloud-based platforms.

  • Should have at least 5 years of experience in quality assurance and/or computerized system validation processes in a regulated environment in life sciences and healthcare (LSHC) industry.
  • Knowledge of and experience with regulatory requirements (e.g. GMP, 21 CFR Part 11, 21 CFR Part 820, EU Annex 11 etc..)
  • Participate as a Validation Subject Matter Expert to support the development of business requirements documentation, technical designs, test strategy and plans, etc.
  • Responsible to set up the validation strategy to ensure agility & speed in delivery
  • Minimum of 5 years of relevant work experience as a Computer System Validation Professional, including hands-on experience with domain systems (Enterprise Level Application i.e., ERP, MRP, QMS, LIMS, etc.) in support of global business operations
  • Should be able to defined and execute end to end validation activities for IT projects and system releases/upgrades
  • Build effective working relationships and collaborate with other domain and enterprise resources to ensure system validation needs are being met.
  • Should be able to create and review applicable validation deliverables such as GxP Assessment, Validation Plan, URS, FRS, DS, Configuration Specification, IQ , OQ , PQ test plan , test report , Validation Summary Report etc.
  • Should have experience in performing Data Migration for validated systems.
  • Exposure to cloud validation , Supplier assessment.
  • Exposure to AI/ML Validation
  • Exposure to Infrastructure Qualification for GxP relevant systems.
  • Periodic Reviews of the IT Systems including user reviews and maintaining the validated state of the IT System
  • Deviation Handling - RCA using 5 x Why approach or any similar approach and CAPA
  • Experience in handle Change Request during operational phase.
  • Requirement Risk Assessment , IT Risk Assessments and Data Privacy related tasks
  • Support Supplier Assessments and provide guidance.
  • End to end validation activities for IT projects and system releases/upgrades
  • Define test strategy and review test cases in accordance with test plan.
  • Support in Internal audit and inspections
  • Participate in project teams and assist in determining project schedules and the appropriate levels of validation.
  • Perform validation functional testing as required. Track and resolve deviations during qualification activities.
  • Test Strategy Definition: Creating a comprehensive testing strategy, including test plans and test data plans across all phases of the SDLC.
PERSONAL ATTRIBUTES
  • Communication: Excellent written and oral communication skills; able to engage with multiple levels of the organization
  • Dealing with Ambiguity: Can effectively cope with change; can shift gears comfortably; can decide and act without having the total picture; remains calm, effective and practical when dealing with ambiguity; doesn't have to finish things before moving on; can comfortably handle risk and uncertainty
  • Self Confidence
  • Good interpersonal skills
  • Ability to collaborate and communicate with stakeholders and external parties.
  • Excellent communication skills - written and oral in English
  • Large degree of flexibility and the ability to work under strong time pressure
  • Inspire and motivate team

Education: BE/Btech/Any fulltime graduation

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