About the Role: We are seeking an experienced L2 Clinical Systems Support Specialist to join healthcare IT support team. In this role, you will provide advanced (L2) technical and functional support for critical clinical applications, primarily used in diagnostic imaging, radiology workflows, oncology, and electronic patient management. You will act as a key point of contact for resolving application-related issues, collaborating with internal teams and vendors to ensure system availability and user satisfaction. Key Responsibilities: Provide Level 2 support for clinical systems, resolving incidents, service requests, and escalations from L1 teams. Troubleshoot application issues, perform root cause analysis, and ensure resolution within agreed SLAs. Support users (clinical and administrative) with application usage, configurations, and minor enhancements. Coordinate with vendors and technical teams for complex problem resolution. Document solutions, contribute to knowledge base articles, and provide training where needed. Support system updates, patches, and validation activities under IT governance. Ensure compliance with healthcare regulations and data privacy standards. Desired Knowledge (Hands-on experience with some of the following): Insignia / Intellirad PACS (Picture Archiving and Communication System) IMS Maxims (Electronic Diagnosis Orders & Patient Administration Systems) Magentus RIS (Radiology Information System) Medilogik EMS (Clinical & Cardiology Reporting Solutions) CIMAR (Cloud-based Medical Image Exchange Platform) iQemo (Oncology Treatment Workflow Solution) IEP (Image Exchange Portal) eRS (Electronic Referral System) Ideal Candidate Profile: 4 plus years of experience in Level 2 application support within a healthcare / clinical systems environment. Strong analytical and troubleshooting skills for healthcare IT systems. Good understanding of clinical workflows in radiology, oncology, and patient referrals. Familiarity with PACS, RIS, and EHR integrations. Experience with ITSM tools (e.g., ServiceNow, Jira) for incident & request management. Knowledge of healthcare compliance standards (e.g., GxP, Data Privacy) is desirable. Excellent communication skills with a customer-centric approach. Ability to work collaboratively in a multi-stakeholder environment. Preferred Qualifications: Bachelor’s degree in Life Sciences, Computer Science, Health Informatics, or related field. ITIL Foundation certification (optional but good to have). Basic understanding of DICOM, HL7 (advantageous but not mandatory). Show more Show less

Mandatory skills: AWS Devops, Kubernetes, Docker, Python scripting (Basic/intermediate), Azure, Basics of citrix (optional) Strong knowledge of Linux/Unix systems and command line tools. Proficiency in scripting languages such as Python, Shell, or Perl. Experience with configuration management tools like Ansible, Puppet, or Chef. Familiarity with cloud platforms like AWS, Azure, or Google Cloud. Understanding of networking principles and protocols (TCP/IP, HTTP, DNS, etc.). Knowledge of containerization technologies (Docker, Kubernetes) and orchestration tools. Expertise in monitoring and logging tools such as Prometheus, Grafana, ELK stack, or Splunk. (Optional - But Good to Know) Experience with Citrix technologies such as XenApp, XenDesktop, and NetScaler Support the administration and engineering of the Citrix environment. Work with Citrix Provisioning Server, SQL Database, and Citrix License Server. Experienced knowledge of virtualization technologies such as VMware or Hyper-V Strong problem-solving and troubleshooting skills, with the ability to analyze and resolve complex technical issues. Excellent communication and collaboration skills to work effectively with cross-functional teams. Strong attention to detail and ability to work in a fast-paced, dynamic environment. Terraform basic syntax and GitLab CI/CD configuration, pipelines, jobs Cloud resources provisioning and configuration through CLI/API Understanding of how to do basic queries in logs tools for general questions Operating system (Linux) configuration, package management, startup and troubleshooting Block and object storage configuration Networking VPCs, proxies and CDNs Show more Show less

About the Role: We are seeking a highly experienced Subject Matter Expert (SME) in Veeva Vault Learning Management System (LMS) to support a major Veeva LMS implementation initiative within a GxP-regulated life sciences environment. The ideal candidate will possess deep expertise in the Learning Management lifecycle, have led or contributed to Veeva LMS deployments, and demonstrated the ability to collaborate with cross-functional teams to build compliant and user-friendly training processes. Key Responsibilities: Serve as the primary SME for Veeva LMS implementation, configuration, and optimization. Lead the analysis of the current Learning Management processes and identify improvement areas, compliance gaps, and inefficiencies. Design and document optimized learning workflows that align with regulatory (GxP) and business requirements. Collaborate with business stakeholders, training leads, and IT teams to capture requirements and ensure effective system integration. Support change management, training plans, and user adoption strategies for the new LMS. Ensure data integrity, audit-readiness, and SOP alignment for learning activities and records. Stay current with Veeva product updates, releases, and industry trends in learning and development within life sciences. Required Skills & Experience: Proven experience as a Subject Matter Expert (SME) in Veeva Vault LMS deployment. Deep understanding of the end-to-end Learning Management lifecycle in a life sciences or pharma setting. Experience in designing and optimizing compliant learning workflows in GxP-regulated environments. Excellent communication and stakeholder management skills. Ability to work across functions including Quality, IT, Regulatory, and Learning & Development teams. Preferred Qualifications: Familiarity with Veeva Vault QMS or DMS is a plus. Experience with Agile or hybrid methodologies in system implementation projects. Bachelor's or Master's degree in Life Sciences, Information Systems, or a related discipline. Show more Show less

Job Summary: We are looking for a seasoned Organizational Change Management (OCM) Lead with hands-on experience driving large-scale change initiatives in multi-site Veeva Vault deployments (QMS, LMS, and DMS). This role will focus on enhancing user engagement, maximizing readiness, and ensuring successful adoption across a global user base. You will play a critical role in shaping the human experience of digital transformation, leveraging feedback loops, behavior change methodologies, and communication frameworks to deliver sustainable results. Key Responsibilities: Lead the global OCM strategy and execution for Veeva Vault (QMS, LMS, and DMS) across a 15,000+ user base. Design and drive user-centric change management plans including stakeholder assessments, readiness plans, training, and communications. Utilize Pulse Surveys and real-time feedback mechanisms to measure engagement, sentiment, and adoption rates. Collaborate with cross-functional teams including Business Process Owners, Quality, Regulatory, IT, and Training Leads. Implement and oversee a communications framework using email, town halls, newsletters, learning platforms, and other internal channels. Lead training design and delivery efforts aligned to adult learning principles and system workflows. Equip and empower end-users to adopt “new ways of working” through clear messaging, hands-on enablement, and continuous support. Champion change resilience and stakeholder alignment at all levels of the organization, including executive leadership. Monitor and report on change adoption KPIs and adjust strategies as needed for optimal outcomes. Required Skills & Experience: 15+ years of experience in Organizational Change Management, with a strong focus on digital system deployments in regulated industries. Proven experience in Veeva Vault (QMS, LMS, DMS) multi-site implementations. Track record of managing change across a large user base (15,000+ users). Deep understanding of change impact assessments, stakeholder mapping, and behavioral adoption strategies. Experience driving human-centered design to increase user engagement and minimize resistance. Strong facilitation, presentation, and coaching skills to engage cross-level stakeholders. Skilled in developing and utilizing Pulse Surveys, user feedback mechanisms, and actionable insights. Knowledge of GxP, 21 CFR Part 11, ISO standards, and validation/compliance frameworks in the life sciences domain. Show more Show less

Role Overview: We are seeking an experienced Subject Matter Expert (SME) – DMS (Veeva Vault) who will be responsible for leading and supporting the deployment and optimization of the Veeva Vault Document Management System (DMS) across global Life Sciences operations. This role requires deep expertise in document lifecycle management, regulatory compliance, and the ability to translate user needs into streamlined, compliant workflows. Key Responsibilities: Serve as the primary SME for the Veeva Vault DMS platform , driving successful deployment, configuration, and optimization. Possess strong knowledge of the documentation lifecycle , including creation, review, approval, release, versioning, archival, and retrieval processes. Assess existing document management processes , identify gaps , inefficiencies , and non-compliance risks , and recommend improvements aligned with industry best practices and regulatory standards (e.g., GxP, 21 CFR Part 11, Annex 11). Collaborate with cross-functional stakeholders, including Quality, Regulatory, IT, and Business teams to gather user requirements , design intuitive workflows, and configure DMS functionality accordingly. Work closely with implementation partners, system integrators, or internal technical teams to design user-friendly workflows that are compliant with applicable regulatory guidelines. Lead or support UAT, training, and change management activities during and post-Veeva Vault DMS implementation. Act as a point of contact for troubleshooting, support, enhancements, and future scalability of the DMS system. Ensure that all documentation processes support data integrity, audit readiness, and regulatory compliance. Required Skills & Qualifications: 8+ years of experience in Document Management Systems, with at least 3–5 years specifically on Veeva Vault DMS in a lead or SME capacity. Strong understanding of Life Sciences documentation processes across R&D, Quality, Regulatory, and Compliance domains. Proven experience in end-to-end Veeva DMS implementation or transformation projects , including configuration, testing, rollout, and post-go-live support. Demonstrated experience in process design, gap analysis, stakeholder engagement, and workflow optimization. Excellent knowledge of compliance requirements and documentation standards relevant to the pharmaceutical or biotech industry. Strong communication, facilitation, and problem-solving skills. Preferred Qualifications: Experience working in regulated environments (GxP) . Veeva Vault certification is a plus . Familiarity with other Veeva modules like QMS or LMS is an added advantage. Experience working with global stakeholders in a matrixed environment. Show more Show less

Job Summary : We are seeking a highly experienced and motivated Subject Matter Expert (SME) for Veeva Vault QMS to lead the deployment and optimization of Quality Management System processes. The ideal candidate will bring deep domain expertise in QMS processes within the life sciences or pharmaceutical industry and will play a critical role in driving compliance, efficiency, and user adoption through effective system design and implementation. Key Responsibilities : Serve as the SME for Veeva Vault QMS , leading deployment, configuration, and optimization efforts. Understand existing QMS processes and workflows; identify gaps, inefficiencies, and areas for improvement. Work closely with stakeholders, business users, and functional SMEs to gather and analyze requirements. Design, implement, and refine QMS processes and workflows that are user-friendly and aligned with global regulatory requirements (e.g., 21 CFR Part 11, GxP, ISO standards). Support validation and testing of QMS functionalities and ensure documentation aligns with compliance standards. Provide training, knowledge transfer, and ongoing support to business and technical teams. Collaborate cross-functionally with IT, Quality Assurance, Regulatory, and Compliance teams. Act as a liaison between business and technical teams to ensure seamless integration and solution delivery. Required Skills & Experience : Minimum 12 years of experience in QMS domain within pharma/biotech/life sciences. Proven experience leading or acting as an SME for Veeva Vault QMS deployment . Deep understanding of Quality Management processes (e.g., CAPA, Change Control, Audit Management, Deviations). Strong knowledge of industry regulations and compliance frameworks (GxP, 21 CFR Part 11, ISO). Excellent communication, stakeholder engagement, and problem-solving skills. Experience in driving process design and change management initiatives. Preferred Qualifications : Veeva Vault QMS certification (if available). Background in Quality Assurance or Regulatory Operations. Experience working in global delivery models (onsite-offshore collaboration). Show more Show less

Role Overview Manage the end-to-end delivery of a Veeva Vault implementation, ensuring compliance with GxP standards, establishing robust governance, and driving Agile adoption with 4-week sprints for user-focused improvements. Responsibilities Lead planning and execution of Veeva Vault (QMS, LMS, DMS) deployment across multiple sites. Establish project governance to ensure compliance with organizational policies and GxP regulations. Implement Agile toolsets for GxP systems, managing 4-week sprints based on user feedback. Collaborate with IT, quality, compliance, and Veeva teams to align deliverables. Mitigate risks and report progress to leadership with clear KPIs. Drive user adoption and training for 15,000+ users. Coordinate with vendors to meet project milestones. Experience: 15+ years in project/program management in pharma/life sciences. Proven leadership in Veeva Vault multi-site deployments (QMS, LMS, DMS) for 15,000+ users. Expertise in project governance and Agile (4-week sprints) for GxP systems. Education : Bachelor’s in Life Sciences, IT, or related field; PMP or Master’s a plus. Skills: Deep knowledge of Veeva Vault and GxP regulations (21 CFR Part 11, EU Annex 11). Proficient in Agile tools (Jira, Confluence) and PM software (MS Project, Smartsheet). Strong leadership, communication, and problem-solving skills. Preferred : PMP, Agile (SAFe/Scrum), or Veeva certifications; experience in change management. Show more Show less

Role Overview: We are hiring a Veeva Vault LMS (VT) Subject Matter Expert to lead and support the design, deployment, and optimization of the Veeva Learning Management System in a regulated Life Sciences environment. The ideal candidate will bring deep domain knowledge of learning lifecycle processes, regulatory training compliance, and hands-on experience in LMS transformation using Veeva Vault Training. Key Responsibilities: Serve as the SME for Veeva Vault LMS (VT) – leading implementation, configuration, and ongoing improvements. Possess a comprehensive understanding of the learning management lifecycle , including training needs analysis, course creation, assignment, tracking, certification, reporting, and compliance. Evaluate existing LMS processes , identify inefficiencies or compliance gaps, and recommend optimized, scalable, and audit-ready solutions. Work closely with cross-functional teams , including Quality, Compliance, IT, HR, and Functional Training leads to gather business requirements and translate them into effective and compliant workflows. Design user-friendly training assignment structures and workflows within Veeva VT that meet regulatory standards (e.g., GxP, 21 CFR Part 11, EU Annex 11). Support or lead activities such as User Acceptance Testing (UAT) , training , and change management for successful adoption. Act as the point of contact for Veeva LMS/VT support , providing expert guidance on enhancements, configurations, and troubleshooting. Ensure all training records and processes are maintained in accordance with regulatory expectations and audit readiness . Required Skills & Qualifications: 12+ years of experience in Learning Management Systems, with 5 plus years of hands-on experience specifically in Veeva Vault LMS / VT . Proven experience in end-to-end LMS lifecycle management within the pharmaceutical, biotech, or medical device industry. Deep understanding of compliance-driven training systems in GxP environments. Experience working as an SME or lead in Veeva LMS implementation , including requirements gathering, configuration, validation, and deployment. Strong experience in process mapping, stakeholder collaboration , and workflow optimization for global LMS processes. Excellent interpersonal, documentation, and presentation skills. Preferred Qualifications: Veeva Vault Training (VT) certification (if available) or strong proof of practical VT expertise. Familiarity with additional Veeva modules like QMS or DMS is an added advantage. Experience working in multi-site, global environments with complex training requirements. Knowledge of 21 CFR Part 11, Annex 11 , and related regulatory standards. Show more Show less

Test Engineer / Test Lead (Veeva Vault) Position Overview: The Test Lead Engineer will spearhead end-to-end testing activities, ensuring thorough application testing and alignment with requirements, while leading and mentoring the testing team. Key Responsibilities: Plan and lead comprehensive testing activities, overseeing the entire testing process. Manage, mentor, and guide the testing team to achieve quality outcomes. Execute and ensure application testing aligns with test protocols and requirements. Collaborate with the validation team to ensure compliance and seamless execution. Leverage expertise in Veeva system testing to maintain high-quality standards. Qualifications: Proven experience in leading and planning end-to-end testing activities. Expertise in application testing and execution per test protocols. Mandatory experience with Veeva system testing. Strong leadership, mentoring, and collaboration skills. In-depth knowledge of testing processes and quality assurance. Show more Show less

Data Migration Engineer /Lead Position Overview: The Data Migration Lead Engineer will lead and execute data migration to Veeva Vault, ensuring data integrity and quality while developing strategies and mapping data from legacy systems. Key Responsibilities: Develop and lead data migration strategies for Veeva Vault from QMS (Caliber, Trackwise, homegrown), DMS (Biovia, Trackwise, Omnidocs), and LMS systems. Oversee end-to-end data migration processes, ensuring quality and integrity pre- and post-migration. Map master data elements from legacy to target systems with precision. Manage and mentor migration teams to achieve seamless execution. Ensure compliance with data migration standards and best practices. Qualifications: Proven experience migrating data to Veeva Vault from diverse QMS, DMS, and LMS systems. Expertise in data migration strategy development and execution. Strong skills in mapping master data elements across systems. Leadership and team management experience. Deep understanding of data integrity and quality assurance processes. Show more Show less

Job Title: Validation Engineer/CSV Consultant (Veeva/Cloud Validation) Location: Mumbai (On-site) Experience: 4-12 years Job Description: We are seeking a skilled Validation Engineer/CSV Consultant to join our Mumbai team, responsible for ensuring compliance of cloud-based systems, particularly Veeva Vault, in the pharmaceutical/medical device industry. Key responsibilities include developing and executing validation protocols (IQ, OQ, PQ), preparing URS, FRS, SOPs, and RTM, and ensuring adherence to FDA, 21 CFR Part 11, and GxP standards. The candidate will conduct risk-based validation, support regulatory audits, and collaborate with cross-functional teams. Ideal candidates will have 4-12 years of experience in computer system validation, hands-on expertise in Veeva Vault configuration/testing, and strong documentation and communication skills.

About the Role: We are seeking an experienced L2 Technical Support Specialist to join healthcare IT support team. In this role, you will provide advanced (L2) technical and functional support for critical clinical applications, primarily used in diagnostic imaging, radiology workflows, oncology, and electronic patient management. You will act as a key point of contact for resolving application-related issues, collaborating with internal teams and vendors to ensure system availability and user satisfaction. Key Responsibilities: Provide Level 2 support for clinical systems, resolving incidents, service requests, and escalations from L1 teams. Troubleshoot application issues, perform root cause analysis, and ensure resolution within agreed SLAs. Support users (clinical and administrative) with application usage, configurations, and minor enhancements. Coordinate with vendors and technical teams for complex problem resolution. Document solutions, contribute to knowledge base articles, and provide training where needed. Support system updates, patches, and validation activities under IT governance. Ensure compliance with healthcare regulations and data privacy standards. Desired Knowledge (Hands-on experience with min 3 of the following): Insignia / Intellirad PACS (Picture Archiving and Communication System) IMS Maxims (Electronic Diagnosis Orders & Patient Administration Systems) Magentus RIS (Radiology Information System) Medilogik EMS (Clinical & Cardiology Reporting Solutions) CIMAR (Cloud-based Medical Image Exchange Platform) iQemo (Oncology Treatment Workflow Solution) IEP (Image Exchange Portal) eRS (Electronic Referral System) Ideal Candidate Profile: 3 plus years of experience in Level 2 application support within a healthcare / clinical systems environment. Strong analytical and troubleshooting skills for healthcare IT systems. Good understanding of clinical workflows in radiology, oncology, and patient referrals. Familiarity with PACS, RIS, and EHR integrations. Experience with ITSM tools (e.g., ServiceNow, Jira) for incident & request management. Knowledge of healthcare compliance standards (e.g., GxP, Data Privacy) is desirable. Excellent communication skills with a customer-centric approach. Ability to work collaboratively in a multi-stakeholder environment. Preferred Qualifications: Bachelor’s degree in Life Sciences, Computer Science, Health Informatics, or related field. ITIL Foundation certification (optional but good to have). Basic understanding of DICOM, HL7 (advantageous but not mandatory).

Role Overview: We are looking for an experienced Senior Medical Writer to develop and lead the creation of high-quality scientific content including manuscripts, abstracts, posters, and congress materials . The ideal candidate will combine strong writing skills with a solid understanding of clinical research and publication standards. Key Responsibilities: Write, review, and finalize scientific content tailored for journals and conferences. Ensure scientific accuracy and strategic alignment across materials. Mentor and guide junior writers, sharing best practices and feedback. Collaborate with clients, authors, and stakeholders to ensure clarity, compliance, and impact. Contribute to digital content development (e.g., infographics, summaries). Support pitches and new business initiatives as needed. Qualifications: PhD/MD/PharmD/MPharm/M.Sc. in Life Sciences or related field. 4+ years in scientific/medical writing with focus on publications. Strong writing, editing, and communication skills. Good understanding of clinical trial data, literature review, and publication ethics. Familiarity with GPP, ICMJE, and journal/congress guidelines.

Role Summary: We are hiring a ThingWorx Developer to build and support IIoT applications for manufacturing use cases. The role involves mashup and service development, shop-floor integration via OPC UA/Modbus, and backend integration with enterprise systems. Key Responsibilities: Develop ThingWorx applications: mashups, services, and reusable components Integrate with PLCs/HMIs via OPC UA/Modbus TCP/IP Create dynamic visualizations (charts, trends, exports) Connect with SAP , SQL , flat files , and other enterprise systems Manage deployments, upgrades, and migrations of ThingWorx apps Work with Azure cloud , including Blob Storage Write and maintain unit test scripts Skills Required: Hands-on with ThingWorx (mashups, services, templates) Strong in Java , JavaScript , and data integration Experience with industrial protocols (OPC UA, Modbus) Good understanding of SQL and enterprise application integration Azure (especially Blob Storage) experience preferred

Title: Software Engineer (Front End)-Senior/Junior Years of experience: 2-7 years (Multiple Roles) Location: Pune, MH (hybrid) Job Description: JavaScript, TypeScript, HTML and CSS, Redux, MobXresponsive design principles and cross-platform development. Jest or Cypress, Familiarity with RESTful APIs and integrating front-end applications with back-end services. Familiarity with cloud platforms such as AWS, Azure or GCP. Strong knowledge of DevOps practices, including CI/CD pipelines and infrastructure as code. Previous experience in the online gaming or casino industry, with a strong understanding of player behaviour and industry regulations Experience with Angular Experience with mobile application development using React Native. Desired Skills: Experience with Webpack, Babel or other build tools. Understanding of security principles and implementing secure front-end applications. Experience with Test-Driven Development (TDD) and writing unit/integration tests. Experience leading technical discussions and code reviews. Experience as part of an Agile software engineering team.

Role: Full Stack Developer Location: Pune (Hybrid) Years of experience : 3-5 The necessary skills that we require for this role include: 3 to 5 years’ practical experience in the full software development life cycle as a software engineer or software developer. Demonstrates solid understanding of Software Engineering design patterns and/or methodologies. Strong proficiency in object-oriented programming (OOP) principles, with a preference for experience in C# and the .NET framework. Proficient in multiple languages, libraries & frameworks (e.g. C#, JavaScript, Angular, React, Vue, Node.js) Demonstrated experience in designing and building RESTful APIs and microservices. Designing the database schema to store application data efficiently Proficient in working with relational and nonrelational databases (e.g. SQL Server & MongoDB) and writing efficient TSQL queries. Hands on experience with containerization technologies (e.g. Kubernetes & Docker) Familiarity with cloud platforms such as AWS, Azure or GCP. Strong knowledge of Devops practices, including CI/CD pipelines and infrastructure as code. Demonstrates solid understanding of Software Testing fundamentals. Demonstrates consistent passion for Technology and keeping up with the industry. Exceptional attention to detail, ensuring high standards of quality in all outputs Ability to adapt quickly to changing environments and priorities, maintaining effectiveness in dynamic situations Excellent problem solving and analytical skills. Ability to accurately estimate effort and take ownership for time management and delivery. Strong collaboration and communication abilities.

Title: Senior Quality Assurance Engineer Years of Experience: 5-7 years Location: Pune, MH, Hybrid Job description: Primary Skills: ISTQB Foundation Level Experience in working with agile teams and successfully delivering agile based software projects. Utilizing dev tools like Visual Studio and Visual Studio Code. Comfortable with source control tools, like GitLab. Ability to write integration and UI tests. Experience using automation frameworks and tools like Playwright, Selenium (NOT IDE), Nunit. Experience in using Typescript/JavaScript, C#, JSON. API Testing using Postman or in code. Experience with designing, creating, and maintaining automation frameworks. Communication skills - ability to communicate with clients, peers and line management Experience of agile and the Scrum or Kanban methodology Advanced Experience with test automation tools and strategies Advanced Experience of using BDD effectively Advanced proven experience with C#/Java and JavaScript Experience with any of the following Frameworks: WebDriver (not IDE) / WebDriver.IO / Cypress / TestCafe / RestShap / Rest Assured Experience with CI/CD pipelines for continuous testing. Dedicated to staying updated on the latest testing tools and technologies, with the ability to adapt to new frameworks as needed. Secondary Skills: ISTQB Advanced Level Certifications Previous exposure to Microsoft Azure DevOps & VSTS Experience with actively developing & managing Docker infrastructure. YAML / Kubernetes Cloud (Azure), Azure DevOps. Knowledge of Message Broker Systems Comfortable with using Kibana, Grafana Capable of reading and writing Mongo collections. Exposure to Saucelabs/BrowserStack or similar tools for mobile testing

Job Summary : We are seeking a highly experienced and motivated Subject Matter Expert (SME) for Veeva Vault QMS to lead the deployment and optimization of Quality Management System processes. The ideal candidate will bring deep domain expertise in QMS processes within the life sciences or pharmaceutical industry and will play a critical role in driving compliance, efficiency, and user adoption through effective system design and implementation. Key Responsibilities : Serve as the SME for Veeva Vault QMS , leading deployment, configuration, and optimization efforts. Understand existing QMS processes and workflows; identify gaps, inefficiencies, and areas for improvement. Work closely with stakeholders, business users, and functional SMEs to gather and analyze requirements Design, implement, and refine QMS processes and workflows that are user-friendly and aligned with global regulatory requirements (e.g., 21 CFR Part 11, GxP, ISO standards). Support validation and testing of QMS functionalities and ensure documentation aligns with compliance standards. Provide training, knowledge transfer, and ongoing support to business and technical teams. Collaborate cross-functionally with IT, Quality Assurance, Regulatory, and Compliance teams. Act as a liaison between business and technical teams to ensure seamless integration and solution delivery Required Skills & Experience : Minimum 8 years of experience in QMS domain within pharma/biotech/life sciences. Proven experience leading or acting as an SME for Veeva Vault QMS deployment . Deep understanding of Quality Management processes (e.g., CAPA, Change Control, Audit Management, Deviations). Strong knowledge of industry regulations and compliance frameworks (GxP, 21 CFR Part 11, ISO). Excellent communication, stakeholder engagement, and problem-solving skills. Experience in driving process design and change management initiatives. Preferred Qualifications : Veeva Vault QMS certification (if available). Background in Quality Assurance or Regulatory Operations. Experience working in global delivery models (onsite-offshore collaboration).

Data Migration Engineer /Lead Position Overview: The Data Migration Lead Engineer will lead and execute data migration to Veeva Vault, ensuring data integrity and quality while developing strategies and mapping data from legacy systems. Key Responsibilities: Develop and lead data migration strategies for Veeva Vault from QMS (Caliber, Trackwise, homegrown), DMS (Biovia, Trackwise, Omnidocs), and LMS systems. Oversee end-to-end data migration processes, ensuring quality and integrity pre- and post-migration. Map master data elements from legacy to target systems with precision. Manage and mentor migration teams to achieve seamless execution. Ensure compliance with data migration standards and best practices. Qualifications: Proven experience migrating data to Veeva Vault from diverse QMS, DMS, and LMS systems. Expertise in data migration strategy development and execution. Strong skills in mapping master data elements across systems. Leadership and team management experience. Deep understanding of data integrity and quality assurance processes.

Test Engineer / Test Lead (Veeva Vault) Position Overview: The Test Lead Engineer will spearhead end-to-end testing activities, ensuring thorough application testing and alignment with requirements, while leading and mentoring the testing team. Key Responsibilities: Plan and lead comprehensive testing activities, overseeing the entire testing process. Manage, mentor, and guide the testing team to achieve quality outcomes. Execute and ensure application testing aligns with test protocols and requirements. Collaborate with the validation team to ensure compliance and seamless execution. Leverage expertise in Veeva system testing to maintain high-quality standards. Qualifications: Proven experience in leading and planning end-to-end testing activities. Expertise in application testing and execution per test protocols. Mandatory experience with Veeva system testing. Strong leadership, mentoring, and collaboration skills. In-depth knowledge of testing processes and quality assurance.