Job Summary: We are seeking a skilled and experienced IBM SAP Solution Architect Lead to spearhead SAP transformation initiatives on IBM Cloud. In this role, you will architect enterprise-grade solutions, lead SAP migration projects, streamline integration across platforms, and support DevOps automation initiatives. Youll act as a key technical leader aligning stakeholders, developers, and business goals within complex cloud and hybrid SAP environments. Job Details: Location: Bengaluru Experience: 6 to 10 Years Employment Type: Full-Time Work Mode: Onsite/Hybrid - 3 Days at office in a Week Office Location - Indira Nagar Key Responsibilities: Lead SAP S/4HANA transformation programs, ensuring seamless delivery on IBM Cloud. Design enterprise architecture and integration strategy for SAP and non-SAP systems. Automate SAP landscape operations using Ansible, Python, Terraform, and GitHub pipelines. Drive test strategy and execution across SAP functional and non-functional domains. Coordinate SAP migrations, ensuring performance, HA/DR architecture, and business continuity. Develop and publish SAP reference architectures and documentation for IBM Cloud. Collaborate with stakeholders and manage technical discussions and roadmap planning. Implement process automation for infrastructure and SAP applications using modern tools. Required Skills & Experience: 6-10 years of experience in SAP architecture, S/4HANA implementation, and migration. Strong hands-on experience with Ansible, Terraform, Python, GitHub, and CI/CD tools. Deep understanding of SAP BTP, LAMA, and integration strategies in hybrid environments. Solid grasp of SAP high availability/disaster recovery architecture. Experience working with databases: HANA, DB2, ASE Sybase, MaxDB, Oracle, MS SQL. Exposure to automation scripting (Shell, PowerShell, Bash, Python). Familiar with tools like JIRA and version control systems (Git). Preferred Certifications: TOGAF SAP OS/DB Migration SAP Cloud Platform Technology IBM Cloud / AWS / Azure / GCP certifications Education: Bachelors degree in Computer Science, Information Systems, Engineering, or related field.
Job description Role QMS Analyst Responsibilities : Assurance/Management (Pharma or Biotech industry) Notice Period: Immediate joiners only We are looking for a QMS professional to assist in drafting investigation reports and supporting quality management processes within the pharmaceutical industry. If you have hands-on experience with Change Controls, CAPAs, and QMS documentation, this role is perfect for you! Key Responsibilities: Write/re-write Investigation reports and participate in root cause analysis specific to Engineering QMS events/incidents/deviations. Support the QA/QMS Leads in daily operations and quality management tasks. Assist in creating, reviewing, analyzing, and closing QMS records (Change controls, CAPAs, documentation). Track, follow up, and report on the status of QMS records. Collaborate with technical SMEs to gather necessary information for drafting investigation reports. Experience & Skills Required : 1-3 years of experience in quality assurance or quality management within the pharmaceutical or biotech industry. Extensive experience drafting Investigation reports for Engineering QMS events/deviations/incidents. Familiarity with Quality Management Systems (QMS), Change Controls, CAPAs, and related processes. Awareness of regulatory requirements (FDA, EMA) and industry standards (ISO 9001, ICH Q10). Understanding of GxP (Good Manufacturing Practices, Good Laboratory Practices, Good Clinical Practices). Strong written and verbal communication skills. Education & Training : Bachelors degree in Biotechnology, Pharmacy, Computer Science, Life Sciences, or a related field. Why Join? Grow your career in the thriving pharma/biotech industry. Gain valuable experience in quality management and regulatory compliance Industry Type: Pharmaceutical & Life Sciences Employment Type: Full Time, Permanent Education UG: Any Graduate Key Skills CAPA, Change Control, QMS, Investigation. Deviation. GxP
Role CSV Engineer Responsibilities Serve as an SME in CSV processes and best practices Develop and execute validation protocols (IQ/OQ/PQ) for computer systems, software applications, and automated processes. Create validation plans, test scripts, and summary reports. Ensure all computer systems comply with FDA regulations, GxP guidelines, and other relevant industry standards (e.g., 21 CFR Part 11). Provide training to staff on CSV processes and regulatory requirements Stay updated on industry best practices, regulatory changes, and advancements in technology related to CSV. Identify opportunities for improving validation processes and procedures. Perform Change Impact Assessments, Risk Assessments, Periodic Reviews . NOTE: Experience in Validation of Lab Systems and Manufacturing Systems is a MUST. Preferred candidate profile 1-3 years of overall experience in computer system validation within the pharmaceutical, biotech, or medical device industry. Strong knowledge of FDA regulations, GxP guidelines, and industry standards (e.g., 21 CFR Part 11, GAMP 5). Proficiency in developing and executing validation protocols and related documentation. Proficient in using validation tools and software. Strong written and verbal communication skills. Education and Trainings Bachelors degree in Biotechnology, Pharmacy, Computer Science, Engineering, Life Sciences, or a related field. Advanced degrees or certifications in validation, quality assurance, or regulatory compliance are a plus.
Responsibilities Serve as an SME in CSV processes and best practices Develop and execute validation protocols (IQ/OQ/PQ) for computer systems, software applications, and automated processes. Create validation plans, test scripts, and summary reports. Ensure all computer systems comply with FDA regulations, GxP guidelines, and other relevant industry standards (e.g., 21 CFR Part 11). Provide training to staff on CSV processes and regulatory requirements Stay updated on industry best practices, regulatory changes, and advancements in technology related to CSV. Identify opportunities for improving validation processes and procedures. Perform Change Impact Assessments, Risk Assessments, Periodic Reviews . NOTE: Experience in IT Systems Validation is a must. Specifically experience with LMS(Learning Management System) is must. Preferred candidate profile 5-6 years of overall experience in computer system validation within the pharmaceutical, biotech, or medical device industry. Experience with validation of IT Systems(LMS). Knowledge in process required for GxP and Non-GxP systems/features. Strong knowledge of FDA regulations, GxP guidelines, and industry standards (e.g., 21 CFR Part 11, GAMP 5). Experience working with cross function teams. Proficiency in developing and executing validation protocols and related documentation. Proficient in using validation tools and software. Strong written and verbal communication skills. Education and Trainings Bachelors degree in Biotechnology, Pharmacy, Computer Science, Engineering, Life Sciences, or a related field. Advanced degrees or certifications in validation, quality assurance, or regulatory compliance are a plus.