Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Indianapolis, INDescription Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Verista in Indianapolis is seeking a CQV Engineer to support change control and deviation management within a regulated cGMP environment. You will collaborate with cross-functional teams to ensure changes are properly assessed, documented, and executed, with hands-on
CVS Health in the United States is seeking a Senior Manager to lead Medical & Pre-Payment Policy deviation management. You will oversee governance, interpretation of policies, and audit-ready documentation, collaborating with Product, Plan Sponsor, Provider Network, Clinical,
Verista is seeking an entry-level Deviation Investigator / CQV Engineer in the Pharma sector. Based in Indianapolis, IN, you will be trained on Deviation Investigation as part of a growing team focused on enabling life sciences clients to
We are seeking a CQV Engineer to support change control and deviation management activities. This role will play a critical part in maintaining compliance, supporting quality systems, and ensuring manufacturing changes are properly assessed, documented, and executed
Verista is hiring an entry-level Deviation Investigator / CQV Engineer in the pharmaceutical sector. The role includes training on deviation investigations and working with project teams to assess and document issues. The position requires strong communication, teamwork, and
Verista is hiring an entry-level Deviation Investigator / CQV Engineer for the pharma sector. The role includes on-the-job training in Deviation Investigation and collaboration with a team of professionals to support quality systems. The position is onsite in
Validation Engineer / CQV Engineer - Change Control & Deviations Indianapolis, IN Veristas 500 experts team up with the worlds most recognizable brands in the life science industry to solve their business needs. The nature of our
Veristas 500 experts team up with the worlds most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community
What Nuclear Manufacturing contributes to Cardinal Health Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Nuclear Manufacturing is responsible
Job Summary The Principal Technical Operations Engineer (Radiopharmaceuticals) is responsible for leading and managing the development, implementation, and continuous improvement of processes within radiopharmaceutical operations. This role is critical for ensuring product quality, regulatory compliance, and
Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love
The Manufacturing Supervisor is responsible for overseeing production operations, ensuring that all work completed is within appropriate timeframes, delivering daily expectations and assignments. Providing on floor support and review of MBR’s, providing coaching and feedback to
Overview People. Passion. Pride. This is what has driven our teams since 1833. Since that time, we have developed to become a critical partner in the global aviation industry, delivering time-critical logistics services at over 300
Working closely with the Quality Manager, the QA Associate will be instrumental in ensuring site compliance with Regulations, ISO Standards, organizations SOPs as well as support in championing and developing organization’s Quality Mindset, as well as
Job Description SummaryLocation: Indianapolis, Indiana Join Novartis and play a pivotal role in shaping the future of Radioligand Therapy manufacturing. As the Site QC Head, you will lead and inspire a high-performing Quality Control organization at
BandLevel 5 Job Description SummaryLocation: Indianapolis, Indiana Join Novartis and play a pivotal role in shaping the future of Radioligand Therapy manufacturing. As the Site QC Head, you will lead and inspire a high-performing Quality Control
What a Sr. Specialist, QC Microbiology contributes to Cardinal Health: Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Control is responsible for the