The Senior Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance Qualification (Stage 2), and Continued Process Verification (Stage 3) activities across the site. This role is responsible for ensuring validation protocols, risk assessments, PPQ studies, and
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 practices (cGMP)
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 employees around the world work to discover and bring
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
Job Description Job Title: Controls Systems Engineering Quality and Process Assurance Working Pattern: Hybrid/Onsite 3 days/week Working location: Indianapolis, IN As the Control System Engineer for Quality, you will independently assure the product has been developed in
The Senior Quality Validation Specialist provides Quality Assurance oversight of validation activities across the site, with a focus on new equipment commissioning and qualification, equipment change controls, and equipment life cycle documentation. This role is responsible for ensuring
At Cardinal Health, were developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities. What a Sr.
Anticipated End Date:2026-07-24 Position Title:Patient Safety DRG Clinical Validation Auditor Job Description: Location: This role enables associates to work virtually full-time, except for required in-person training sessions, providing maximum flexibility and autonomy. This approach promotes productivity, supports
Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you’ve 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
Senior Business Process Lead Financials The Senior Business Process Lead Financials is a Finance-led business process owner responsible for identifying business process capability gaps, standardizing business processes, defining and prioritizing Oracle ERP-enabled capabilities for the Financials workstream. This role leads
Job Summary We are seeking a Manufacturing Process Engineer with at least 3 years of experience in the Medical Device industry to support manufacturing operations, process optimization, and continuous improvement initiatives. The ideal candidate will be responsible for
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
Senior Director Embedded Systems and Process Engineering (ESPE) At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision,
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
Startup And Validation EHS Team Lead ERM is hiring an experienced Startup and Validation EHS Team Lead for onsite support of our clients new greenfield pharmaceutical manufacturing facility in Lebanon, IN. The ideal candidate will bring strong leadership,
Job Description ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT
Role Summary Responsible for delivering solutions to manufacturing areas with improvement needs across process readiness, robustness, efficiency, and effectiveness. This role focuses on implementing improvement activities and corrective actions to ensure maximum quality, eliminate waste, and increase
Patient Safety DRG Clinical Validation Auditor Location: This role enables associates to work virtually full-time, except for required in-person training sessions, providing maximum flexibility and autonomy. This approach promotes productivity, supports work-life integration, and ensures essential face-to-face
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 employees around the world work to discover and bring