7 Gcps Jobs

You will be working as a full-time Neo4j Graph Developer in a company that is a Neo4j certified Service Solution partner. Your main responsibilities will include designing and developing graph-based applications, implementing back-end services, optimizing graph databases, and writing efficient code. It is essential for you to have expertise in Neo4j/Tiger Graph, experience with GCP's ETL related services, hands-on experience with K8s, and previous work in Agile methodology. Additionally, you will need to spend 2 days a week working from the office in either Pune or Bengaluru. Your role will involve close collaboration with the team to ensure the smooth integration and performance of the graph database system.,

NTT DATA is looking for a Senior Quality Engineer to join their team in Pune, Maharashtra, India. As a Senior QE, you will play a crucial role in ensuring that digital solutions are defect-free and impactful for clients. By delivering automated testing solutions, you will contribute to the success of products, customers, and services. Joining the Quality Engineering practice at NTT DATA is not just a job but an opportunity to grow your career. You will receive training on quality assurance practices, programming languages, test automation tools, and certifications to enhance your skills and deliver valuable work. As a Senior Quality Engineer at NTT DATA, your responsibilities will include overseeing test management, designing and executing test automation frameworks, conducting performance testing, analyzing test results, collaborating with project teams, managing test environments, resolving integration issues, reviewing code coverage, managing defects, customizing automation frameworks, and implementing testing strategies for large-scale system software. Basic qualifications for this role include 6+ years of experience in test automation using tools like Selenium, Java, Cucumber, and REST Assured, as well as experience in software testing and writing automation scripts. You should also have knowledge of test automation tools, performance testing tools, and experience with messaging systems like AMQ, WMQ, and Kafka. Preferred qualifications include advanced skills in performance testing tools, experience in ADO pipeline setup, knowledge of Behavior-Driven Design principles, and leadership experience. The ideal candidate for this role is a lifelong learner, a team player, and a strong communicator. You should be curious, resourceful, and eager to tackle new challenges. If you are passionate about quality engineering and are looking to grow your career in a dynamic and innovative environment, apply now to join NTT DATA's team in Pune, India. Please note that the shift timing requirement for this role is 1:30 pm IST - 10:30 pm IST.,

Responsibilities Main point of client contact and study team for all DM related matters Execute all DM start-up activities, including the development and maintenance of eCRFs Define and create data listings, summary table validation, data specifications, and process data transfers for statistical review Ensure clinical data within EDC is in quality to lock/unlock and freeze/unfreeze as appropriate for statistical review, interim review, and or final database lock Set and create the data base and support the development of the study eCRF and then validate them, assessing the correct functionality of the eCRF developed, in compliance with the applicable quality validation standards Coordinate and execute the coding activities (by using the known dictionaries, e.g. MeDRA, WHO etc), drug safety reconciliation and data review Qualifications Min 5 years relevant data management experience in the CRO/pharmaceutical industry required EDC experience required Proven ability to use statistical software - SAS Demonstrates knowledge of GCPs and protocol Strong time management and prioritisation skills to meet deadlines Strong project management & communication skills (verbal/written) Experience in pharmacology and drugs life cycle Knowledge of ICH-GCP Strong analytic and quantitative background Excellent Microsoft Office Skills Show more Show less

Summary Of Responsibilities Works with internal teams to progress quality issues in QMS. Tracks timeliness of cases in QMS. Supports teams in creation of CAPAs. Maintains strong working knowledge of QMS. Interacts with QA Lead Manager and above as required for quality issue case progression and client notifications. Supports QA Lead Manager and above in pulling metric data, trending, and tracking of QI. All other duties as needed or assigned. Qualifications (Minimum Required) A minimum of a bachelors degree in Life Sciences preferred (or equivalent Life Science experience). Experience (Minimum Required) 8 years in regulatory environment (experience in GXP roles). Strong understanding of QMS and CAPA process. Ability to work well within a team environment. Convey key details of quality issues internally. Communicate quality issue summary to clients where applicable. Knowledge of GCPs/GXPs. Preferred Qualifications Include Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Physical Demands/Work Environment Travel may be required. Office-Based (Hybrid), as requested by the line manager. Learn more about our EEO & Accommodations request here. Show more Show less

As a Data Management leader, you will take charge of studies and oversee the development of project documentation, system setup, data entry, and validation procedures for junior staff. Your responsibilities will encompass all Data Management activities from study initiation to database lock, ensuring adherence to client quality standards, project timelines, and budgets. You will collaborate directly with Sponsors to understand their specific needs and lead the implementation of those requirements. Additionally, you will conduct regular reviews of client processes to ensure they align with Sponsor and Fortrea's expectations. You will lead various studies involving healthy volunteers and patient populations, multi-site projects, and client management with reduced timelines. Your role will entail efficiently organizing and prioritizing workload and deliverables. You will be accountable for all Data Management deliverables within set timelines, guiding your team and reviewing their output to maintain the highest quality. Ensuring strict compliance with protocols, SOPs, and GCP standards for allocated projects will be crucial. Collaboration with Project Managers to establish timelines aligned with contracted milestones, communication with leads from different disciplines, and leading internal project team meetings are essential aspects of your role. Proactively identifying risks, coordinating deliverables, and keeping stakeholders informed of project progress will be key responsibilities. You will also support risk mitigation strategies, maintain client relationships, and review satisfaction surveys. In addition, you will provide leadership, mentorship, and coaching to the internal study team in DM processes, support performance evaluations, and stay updated on industry technologies for process improvement. Your role will involve maintaining accurate records, performing database reconciliations, representing DM in new business opportunities, and addressing audit findings promptly. Qualifications: - University/college degree or relevant experience - 6 to 8 years of Data Management experience with sponsor management experience - Fluent in English Preferred Qualifications: - Degree in life sciences, health sciences, or information technology - Knowledge of clinical trial processes, biometrics, and electronic data capture - Understanding of medical terminology and scientific background Physical Demands/Work Environment: - Office and home-based work - Overtime and weekend work may be required - Flexible shifts as per business needs As a Data Management leader at Fortrea, you will play a vital role in ensuring the success of studies by effectively managing data-related activities, fostering client relationships, and driving process improvements.,

As a Senior Quality Engineer at NTT DATA, you will play a vital role in ensuring the successful delivery of defect-free digital solutions to our clients, enabling them to thrive in today's competitive market. Your responsibilities will include overseeing test management, designing and executing test automation frameworks, conducting performance testing, analyzing test results, and collaborating with various teams to ensure the quality and integrity of applications. Joining our Quality Engineering practice is not just a job but an opportunity for career growth. You will be equipped with the necessary skills to implement enterprise-grade test automation, produce robust applications, and continuously enhance your capabilities. We will provide training on quality assurance practices, new programming languages, test automation tools, and support you in obtaining relevant certifications to further advance your expertise. Once you are part of our team, you will be involved in various aspects of test management, automation, performance testing, results analysis, collaboration, environment management, issue resolution, code coverage, defect management, automation framework customization, and testing strategies for large-scale system software. Your role will also require expertise in Cargo Platform, UI Path automation tool, performance testing tools, messaging systems, OpenShift, Kubernetes, and test management tools like Jira, Azure DevOps, or HP ALM. We are looking for individuals with at least 6 years of experience in overall test automation, CargoWise proficiency, UI Path automation tool expertise, and a strong background in designing functional and end-to-end test cases. Knowledge of performance testing tools, messaging systems, OpenShift, Kubernetes, and test management tools is also essential. Preferred qualifications include advanced skills in performance testing tools, ADO pipeline setup experience, software testing automation skills, and proficiency in BDD principles using tools like Cucumber. The ideal candidate for this role is a lifelong learner, a team player, and an effective communicator. You should be proactive, resourceful, and willing to take on new challenges. If you are passionate about delivering high-quality digital solutions and eager to contribute to a dynamic and innovative team, we encourage you to apply for this exciting opportunity. Please note that this position requires working hours from 1:30 pm IST to 10:30 pm IST. Join NTT DATA, a global leader in business and technology services, and be part of a diverse team dedicated to driving innovation, optimizing processes, and transforming businesses for long-term success. Visit us at us.nttdata.com to learn more about our organization and the impactful work we do.,

Job purpose: The Clinical Data Manager is a key member of Ocugens clinical data management team. This individual will be responsible for ensuring quality data collection and management processes, CRF development, database design, data monitoring, and validation of entered data for clinical development, and/or marketed products. This individual will work closely with the Biometrics team and the rest of the team at Ocugen to execute the data collection needs of the research studies. Duties and responsibilities: Establishes data flow from collection to final analysis through a data management plan. Ensures the accurate collection of electronic data. Collaborates on implementation and collection of data supporting for research protocols. Develops data transfer specifications and data review specifications and/or data quality review plan specifications. Develops program standard and study-specific electronic Case Report Forms (eCRFs). Develop and revise SOPs, implement DMP and strategies. Develop and implement risk management strategies. Prepare and participate in Audits. Develops edit checks, validation reports to ensure quality data. Provides input to project timelines and ensures that project timelines for database deliverables are met. Ensures that project tasks are completed with acceptable quality. Ensure all required documentation is completed in a timely manner. Lead junior Data management staff. Collaborates with other functional teams to ensure proper output of clinical data as needed for deliverables. Additional tasks and projects as requested. Qualifications : BS degree in clinical, biological or mathematical sciences, or related field or nursing qualification, or work- related equivalent. 6+ years direct clinical data management experience in pharmaceutical development or CRO environment. Experience with clinical trials. Experience with CRFs, and in the development process of EDC databases, IRT systems and diary applications for data collection. Strong knowledge of GCPs, ICH, FDA, and CDISC regulatory requirements governing clinical studies. Demonstrated attention to detail and outstanding organization skills. Self-motivated with a commitment to high quality, on-time deliverables. Excellent communication and collaboration skills with a team-oriented approach. Demonstrated ability to identify and resolve issues and effectively manage timelines. Experience in working with USA biopharmaceuticals/pharmaceuticals companies or client. Strong communications skills and a track record of accomplishment managing client relationships as well as regulatory agencies for USFDA and EMA. Working conditions : This position operates in an office setting, in person. Remote work will be limited. Job may additionally require incumbent to be available outside of these hours to handle priority business needs. Physical requirements: This is a largely sedentary role.