At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of
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,
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
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
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
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
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 community
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
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
Job Title: Non-Credit Adjunct Instructor: Radioligand Therapy (RLT) Manufacturing & Operations Training Location: Indianapolis Job Type: Contracted Technical Training, Adjunct Instructor Classification: Skills Training Adjunct Faculty Salary Range: Salary varies - Based on qualifications and experience
Job Description SummaryLocation: Indianapolis, Indiana Make a meaningful impact at the forefront of advanced cancer care. As Head of QA Operations, you will lead the Quality Assurance Operations organization supporting Novartis Indianapolis Radioligand Therapy (RLT) Drug
The Retail Service Specialist will support the Store Manager and Assistant Managers in areas of sales, customer service, store appearance, and store operations. This position will also assume shift management responsibilities in the absence of Assistant
At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of
At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of
At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of
Senior Quality Control Compliance Specialist Summary The Senior Quality Control Compliance Specialist plays a vital role on the QC team with analytical and microbiological testing experience. This role will support laboratory processing of finished product, incoming