TSMS – Senior Process Validation Engineer The Senior Process Validation Engineer - Technical Services and Manufacturing Sciences (TSMS) will be responsible for leading all facets of Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing
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
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
Are You Ready? CAI is a professional services company established in 1996 that has grown to more than 700 people worldwide. We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness
INCOG BioPharma is seeking a highly motivated Senior Validation Engineer with validation expertise to join our team. The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing validation requirements
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
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
E2i Inc. is seeking a lead investigator to uncover root causes for assigned deviations in a pharmaceutical client environment in Indianapolis, IN. The role involves interviewing operators, engineers, and managers, then developing CAPAs to prevent recurrence. You
Bristol Myers Squibb via RayzeBio is seeking a Senior Validation Engineer in Indianapolis to support GMP radiopharmaceutical operations and CQV execution. You will draft and validate protocols, support new technologies, CAPAs, and continuous improvement initiatives in a fast-paced
# Lead Validation EngineerIndianapolis - RayzeBio - INFind out how well you match with this jobAt RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the
RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Senior Validation Engineer to support a radiopharmaceutical facility in Indianapolis. You will draft and execute CQV documents for GMP spaces, collaborate with project teams, and help drive continuous
Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated
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
A leading company in life sciences is seeking a professional for CQV Execution and Safety. Responsibilities include performing commissioning, qualification, and validation activities, ensuring compliance with documentation, and managing project planning. The ideal candidate will have a
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
RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is seeking a Lead Validation Engineer to support the Radiopharmaceutical facility in Indianapolis. You will lead commissioning, qualification, and validation activities across facility, utility, analytical, and process systems, guiding teams from
Barry-Wehmiller Design Group is seeking a Validation Engineer II to support capital projects and develop validation and FDA compliance documents for pharmaceutical equipment. The role involves traveling to top clients, assisting in designing manufacturing processes, and coordinating project activities
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