1.0 - 2.0 years

0 - 2 Lacs

Bengaluru, Karnataka, India

On-site

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Key Deliverables: Build analytical datasets from multiple data sources for business decision-making Develop statistical and machine learning models aligned with retail functions Create structured algorithms and reusable modules for scalable data solutions Present actionable insights through intuitive dashboards or presentation tools Role Responsibilities: Collaborate with functional teams to translate business needs into analytical use cases Apply CI tools to identify and drive operational improvements Ensure quality and timeliness of deliverables against defined KPIs Create visualization layers that enable end-user decision-making across domains

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Senior decision scientist Tesco Plc

2.0 - 4.0 years

2 - 4 Lacs

Bengaluru, Karnataka, India

On-site

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Key Deliverables: Build statistical models and ML algorithms to solve real business problems Translate business challenges into structured analytical frameworks and data solutions Create scalable, reusable code modules and visualization dashboards for decision making Collaborate cross-functionally to enhance analytical adoption and drive continuous improvement Role Responsibilities: Engage stakeholders to gather business priorities and scope data science solutions Leverage multiple data sets to construct analytical models and insights Share best practices and new advancements with team to upskill and innovate Deliver actionable outputs through intuitive tools or presentations for end-users

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Software Validation Engineer / CSV - IT Flex

5.0 - 10.0 years

5 - 9 Lacs

Chennai, Tamil Nadu, India

On-site

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Job Description To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a/an Software Validation Engineer - IT located in Chennai Location. Reporting to the Manager and the role involves What a typical day looks like: Good Experience in executing Medical industries software validations, having led and managed projects. Strong working knowledge of applied statistics, quality systems, and regulatory requirements across multiple health authorities including 21 CFR 820, 21 CFR Part 11, ISO 14971, ISO 13485, FDA, EU Medical Device Regulation, GAMP, GPSV, and CSV/CSA High-level strategic problem-solving and reasoning skills. Analyzes evaluates and presents information concerning findings, trends with IT in business, and development. Ensure adherence to software validation processes and perform review & approval for all the software validation activities. Suggests and debates to implement the right SDLC, software validation methods, and procedures with Flex. Train and coach project team members on achieving quality in project deliverables (e.g. GDP, V&V Process, CSV, project-related risks management, resolving the issues by following the right process, and SOP requirements). Conducts meetings (technical & management) to review investigation findings related to IT systems. Cooperates with other department personnel and peers in understanding needs and identifying opportunities for improvements. Serve as the SME for CSV, maintaining the knowledge and information in the CSV area of expertise. Perform software validation activities Liaise between IT, Quality, Project Team, Corporate Quality team, and various regulatory bodies. Keep abreast of regulatory developments within or outside of the company as well as evolving best practices in compliance control. Prepare reports for senior management and external regulatory bodies as appropriate. Escalate non?compliance with a resolution for the fundamental CSV compliance issues. Support the project team to perform audit readiness and project audits. Expected to travel (domestic/internationally) when needed to meet with Flex facility project Teams. Work collaboratively with different departments located in a different geography. The experience we're looking to add to our team: 5 - 10 years of experience in Medical/Life Sciences industries software validation and compliance reviews. Strong working knowledge of applied statistics, quality systems, and regulatory requirements across multiple health authorities including 21 CFR 820, 21 CFR Part 11, ISO 14971, ISO 13485, FDA, EU Medical Device Regulation, GAMP, GPSV, and CSV/CSA High-level strategic problem-solving and reasoning skills. Analyzes evaluates and presents information concerning findings, trends with IT in business, and development. Ensure adherence to software validation processes and perform review & approval for all the software validation activities. Suggests and debates to implement the right SDLC, software validation methods, and procedures with the Flex.

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