Role Summary The Senior Manager/Associate Director, MSAT/Process Characterization and Validation Readiness will lead AAV process characterization, technology transfer, control strategy development, and PPQ readiness activities across Sf9/baculovirus and HEK-based manufacturing platforms. This role will partner closely with internal CMC
Senior Manager/Associate Director, MSAT/Process Characterization and Validation Readiness The Senior Manager/Associate Director, MSAT/Process Characterization and Validation Readiness will lead AAV process characterization, technology transfer, control strategy development, and PPQ readiness activities across Sf9/baculovirus and HEK-based manufacturing platforms. This role will partner
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Role Summary The Senior Scientist supports development, optimization, and scale-up of AAV manufacturing processes using Sf9/baculovirus and HEK-based systems. This role contributes to early and late-stage CMC activities including process characterization, technology transfer, control strategy development, and
We are seeking a Senior Associate to join the Issue Validation Team within Internal Audit. This is an exciting opportunity to join a dynamic and agile team where members learn from each other and grow together to
Model Validation Senior Manager Strategy, Growth, and Transformation | Functional and Operational Strategy and Transformation Same job available in 3 locations Boston, Massachusetts, United States Chicago, Illinois, United States New York, New York, United States Position Summary
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
The Aspen Group (TAG) is one of the largest and most trusted retail healthcare business support organizations in the U.S. and has supported over 20,000 healthcare professionals and team members with close to 1,500 health and
Job Description The Director, Business Systems Validation External / Automation provides strategic leadership and direction to validation teams within an assigned geography. They oversee performance management, organizational capability building and process optimization. They partner with other leaders on workforce
Application Deadline: 08/16/2026 Address:VIRTUAL(R)32 - HomeRes - NY Job Family Group:Audit, Risk & Compliance Performs validation of models and assesses model risk to confirm model appropriateness and capability for a designated portfolio. Provides effective challenge during model
CoreWeave is The Essential Cloud for AI. Built for pioneers by pioneers, CoreWeave delivers a platform of technology, tools, and teams that enables innovators to build and scale AI with confidence. Trusted by leading AI labs,
Primary Skills: Injection Molding (advanced), Extrusion Blow Molding (advanced), Validation Methodologies (advanced), Root Cause Analysis (advanced), CAPA Execution (advanced) Contract Type: W2 Duration: 12 Months Location: Rochester, NY - 14625 ( - Onsite) Pay Range: $90 -
Computer System Validation Specialist Computer System Validation, CSV, GxP, 21 CFR part 11, Risk Based Approach Roles and Responsibilities 10+ yrs. of experience in Computer System Validation Senior Level individual with GxP experience Ability to lead, fully knowledgeable of
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
CSV for SAP Systems/Projects To create, assign, and track the project module work plans for delivery and also provide technical guidance for work completion. (1.) To ensure process improvement and compliance in the assigned module and participate
Director, Compliance and Validation You will join our East Brunswick, New Jersey office, be part of a committed organization of over 1,500 professionals, and work in teams and directly with our clients doing work that is shaping
AI Risk Management Oversight And Governance The Model Risk Management (MRM) group is a multidisciplinary group of quantitative experts at Goldman Sachs with presence in New York, Dallas, London, Birmingham, Warsaw, Hong Kong, Bangalore, and Hyderabad.
DRG Clinical Validation Lead Virtual: This role enables associates to work virtually full-time, with the exception of required in-person training sessions, providing maximum flexibility and autonomy. This approach promotes productivity, supports work-life integration, and ensures essential face-to-face
Director, Business Systems Validation External / Automation The Director, Business Systems Validation External / Automation provides strategic leadership and direction to validation teams within an assigned geography. They oversee performance management, organizational capability building and process optimization. They partner with
Manager AI Assisted Process, Risks and Controls Transformation Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect, and transform their organization. Join