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
Harba is seeking a qualified individual to lead a team of process validation engineers in Indianapolis, Indiana. This leadership role requires a Bachelors degree in Engineering or Life Sciences, extensive experience in regulatory environments, and proven abilities in
Techtrueup is seeking a Manufacturing Engineer in Indianapolis, IN, for a 6-month contract, focusing on supporting medical device manufacturing processes. The role involves developing validation strategies, ensuring compliance with FDA and ISO standards, and collaborating with cross-functional
Job Responsibilities Lead, develop, and oversee a team of process validation engineers, providing direction on both technical execution and professional growth Establish team objectives, conduct performance reviews, and implement development plans to strengthen individual and group capabilities Partner
Vonco Products, LLC in Indianapolis is seeking an Integration (Process Validation) Engineer to lead process validation and manufacturing integration activities for medical device packaging. This role includes developing protocols and ensuring compliance with FDA and ISO standards. The ideal candidate
Aldevron, a Danaher company, seeks a Senior Engineer, Process Validation to lead and support internal and external validation projects that enable commercialization of vital new life-saving medicines. This role reports to the Process Validation Manager and is part of the Technical
Aldevron is seeking a Senior Engineer in Process Validation to lead projects that support the commercialization of life-saving medicines. This role involves designing and executing validation strategies in a remote work setup. The ideal candidate will have over 5
Integration (Process Validation) Engineer Medical Device Contract Manufacturer – Flexible Films & Packaging Position Summary The Integration (Process Validation) Engineer is responsible for leading and supporting process validation and manufacturing integration activities for medical device packaging, flexible film converting, and related manufacturing
Technical Estimator - Industrial Automation & Validation Services Automation | Controls | Instrumentation | Validation (CQV) Location: Indianapolis, IN PACIV ( Process Automation, Controls, Instrumentation & Validation) delivers automation, controls, instrumentation, and validation solutions to manufacturing and regulated industries. For over
Anticipated End Date:2026-08-24 Position Title:Manager of DRG Coding & Clinical Validation Audit Job Description: Manager of DRG Coding Audit-Program/Project Locations: The selected candidate must reside within a reasonable commuting distance of the designated posting location(s): Virginia, Indiana,
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
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
Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know youve got big plans - so do we! Our colleagues across the globe love
If you are wondering what makes Trimedx different, its that all of our associates share in a common purpose of serving clients, patients, communities, and each other with equal measures of care and performance. Everyone is
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
BandLevel 3 Job Description SummaryLocation: Indianapolis, Indiana Are you passionate about solving complex engineering challenges in a highly regulated manufacturing environment? As a Process Engineer II, you will play a vital role in supporting the launch and
We are looking for a Validation Technical Writer who is a detail-oriented documentation professional with a strong technical background and a thorough understanding of GMP documentation standards in a regulated pharmaceutical manufacturing environment. Embedded within INCOG BioPharmas
Manager - Validation Lead Technical Support & Operations Global Services At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our
Manager of DRG Coding & Clinical Validation Audit Manager of DRG Coding Audit-Program/Project Locations: The selected candidate must reside within a reasonable commuting distance of the designated posting location(s): Virginia, Indiana, Georgia, Ohio, Maryland; New Jersey, New