This is a full-time salaried position with Project Farma, a PerkinElmer company. The successful candidate will be willing to travel domestically and internationally, to meet client project requests. Project Farma’s purpose is to improve patient lives
We are actively seeking a Principal QA Process Validation Specialist to provide technical Quality oversight and subject matter expertise for process validation activities supporting aseptically filled drug products. This role is ideal for a Process Validation Engineer or Validation SME with strong technical
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
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
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
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
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
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 & PackagingPosition 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 processes.
Kimball Electronics in Indianapolis, IN is seeking a Sr. Injection Mold Process Engineer to develop, implement, and support injection molding processes that meet quality, cost, and delivery goals for our customers. The role emphasizes root-cause analysis, process improvements,
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
Job Description Job Title: Technical Lead - Systems Engineering, Validation and Verification, T56/501K and Helicopters Programs Working Pattern: Fulltime Working location: Indianapolis, IN Relocation assistance will be provided if applicable Why Rolls-Royce? At Rolls-Royce we are proud