VP of Revenue
VP, Revenue/Development Katalyst Group is recruiting for a newly created VP, Revenue/Development for a nonprofit... career opportunity, please submit your resume via the Katalyst Group Careers page ( ) or email your resume directly...
VP, Revenue/Development Katalyst Group is recruiting for a newly created VP, Revenue/Development for a nonprofit... career opportunity, please submit your resume via the Katalyst Group Careers page ( ) or email your resume directly...
Roles & Responsibilities: Lead cost optimization initiatives across supply chain and procurement functions, ensuring measurable savings. Coordinate cross-functional teams to drive efficiency in sourcing, vendor management, and logistics....
Roles & Responsibilities: Writing and execution of validation protocols and reports (ie. IQ, OQ, PQ, etc.) Developing and implementing manufacturing processes, preparation of specifications and operator instructions, process studies, pro...
Job Summary: As a Computer System Validation (CSV) Engineer in the pharmaceutical industry, this role is responsible for ensuring that computer-based systems such as Manufacturing Execution Systems (MES), process control software, and aut...
Roles & Responsibilities: Own end-to-end deviation investigations and effectively collaborate cross-functionally to ensure a thorough, risk-based investigation is conducted for each quality event commensurate with the event classification...
Summary : The Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects and takes ...
Responsibilities: The Regulatory Manager (RM) provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, pediatric planning, and accelerated procedures, e...
Responsibilities: Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. Provide strategic oversight and direction to CRO clinical data m...
Job Summary: Responsible for manufacturing and assembling clinical and commercial products. Operates production equipment. Weighs, measures and checks raw materials to ensure batches manufactured contain proper ingredients and quantities. ...
Roles& Responsibilities: Lead the development, execution, and approval of validation master plans, validation plans, IQ/OQ/PQ protocols, and final reports, with emphasis on sterilization, endotoxin control, and microbiology-related proces...