3 Csv Deliverables Jobs

As an experienced professional with over 10 years of expertise in Lab Vantage LIMS, you will be proficient in working with tools such as bartender, executing SQL queries, and managing CSV deliverables. Your role will involve conducting CSV activities including IQ, OQ, and PQ, while gaining hands-on experience in SaaS environments, with a preference for Lab Vantage. Responsibilities: - Working on bartender - Executing SQL queries - Managing CSV deliverables - Conducting CSV activities such as IQ, OQ, and PQ - Gaining hands-on experience in SaaS environments Qualifications: - Experience with Lab Vantage LIMS Required Skills: - Good knowledge of CSV deliverables - Good knowledge of CSV activities such as IQ, OQ, and PQ - Hands-on experience in SaaS environments Preferred Skills: - Experience with Lab Vantage Join us in this role where your expertise in Lab Vantage LIMS and strong understanding of SQL queries will be valuable assets for the team.,

Summary Oversee all aspects of quality management and ensure the highest level of compliance across our projects About The Role Major accountabilities: Oversee & support all areas of quality management for GxP/non GxP Systems. Drive the validation process, including validation planning, testing (IQ/OQ/PQ), and validation reporting. Support Authoring, reviewing, and approving of CSV deliverables for accuracy, consistency, clarity and completeness. Ensuring all the validation SOP/Work Procedures are followed during the application development. Coordinate with project managers and teams to ensure the alignment of project outputs with quality standards. Evaluate data and QM processes to identify improvements to enhance efficiency and accuracy. Manage change control processes for tool updates and deployments while driving continuous improvements in validation and quality workflows. Support in audits and inspections to ensure adherence to compliance regulations and industry standards. Create and maintain documentation of processes and validation activities and provide training to teams on quality standards and procedures. Oversee root cause analysis, corrective actions, and preventive actions to address quality issues. Ensure all systems and software used meet industry regulations and data integrity rule Minimum Requirements Minimum of 10 years experience in Quality Management, ideally within the Pharma or any regulated industry. Proven experience in managing GxP/non GxP projects from requirement definition to retirement. Working experience in all lifecycle stages of IT system(including System retirement) would be preferred. Ability to drive innovative validation strategies for business initiatives Knowledge of IT systems and software used within the Pharma industry. Exceptional leadership skills with the ability to drive a team towards meeting quality standards. High attention to detail with the ability to identify potential risks or issues. Solid interpersonal skills, including the ability to build and maintain effective working relationships. Ability to influence and drive collaboration across all levels of the organization. Bachelor&aposs degree in IT, Pharmacy or related field. Why Novartis: Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Youll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment To Diversity And Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [HIDDEN TEXT] and let us know the nature of your request and your contact information. Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients lives. Ready to create a brighter future together https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways well help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Show more Show less

You will be responsible for overseeing all aspects of quality management and ensuring the highest level of compliance across projects. This includes driving the validation process, supporting the authoring, reviewing, and approving of CSV deliverables, coordinating with project managers to align project outputs with quality standards, and managing change control processes for tool updates and deployments. Additionally, you will evaluate data and QM processes for improvements, support audits and inspections for compliance, oversee root cause analysis and corrective actions, and provide training on quality standards and procedures. Minimum Requirements: - Minimum of 10 years experience in Quality Management, preferably in Pharma or regulated industries. - Proven experience in managing GxP/non GxP projects from requirement definition to retirement. - Working experience in all lifecycle stages of IT systems, including System retirement. - Ability to drive innovative validation strategies and knowledge of IT systems in the Pharma industry. - Exceptional leadership and interpersonal skills with attention to detail. - Bachelor's degree in IT, Pharmacy, or related field. Novartis is committed to diversity and inclusion in the workplace, creating an outstanding work environment that reflects the patients and communities served. The company also provides accessibility and accommodation for individuals with disabilities, aiming to support reasonable accommodations during the recruitment process. If you are interested in staying connected with Novartis for future career opportunities, you can join the Novartis Network. Additionally, you can learn more about the benefits and rewards offered by Novartis in the Novartis Life Handbook.,