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
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
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re seeking a Process Controls & Validation Engineer with a strong background in cGMP validation, who can develop sound
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
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
Performance Validation is a 100% employee-owned consulting firm focused on CQV services for the life sciences industry. You will be embedded in project teams, learning on real client engagements, and progressively taking on responsibility across the full
Responsibilities Lead migration of legacy documents into Kneat digital platform, ensuring compliance and consistency. Qualify redundant lab equipment (e.g., pH meters, thermal mixers, peristaltic pumps, nutating mixers) to ensure operational integrity. Perform equipment and temperature mapping
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
# Senior 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
1 day ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. This range is provided by CAI. Your actual pay will be based on your skills and experience
Start Your Engineering Career Where It Actually Matters Most engineering jobs ask you to specialize early and stay in your lane. This one is different. At Performance Validation, youll work directly in FDA-regulated facilities such as pharmaceutical
Draper seeks a Senior Analog ASIC Validation Engineer in Cambridge, Massachusetts to specify, design, verify, test and validate ASICs from concept to first silicon and through manufacturing support. The role emphasizes analog and mixed-signal expertise, test plan development,
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
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
This role will be based out of the Ambu America’s Center of Excellence located at the Noblesville, Indiana manufacturing facility. The role has responsibility for Advanced Manufacturing Engineering functions of both the Noblesville, IN and the
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