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...
Summary : As a Computer System Validation (CSV) Engineer specializing in the pharmaceutical industry, you will ensure that computer-based systems such as Manufacturing Execution Systems (MES), process control software, and automation plat...
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...
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...
Job Summary: Must have at least 10 years of experience Must be bilingual (English/Spanish) Someone that can generate VMP, develop systems lists, provide all necessary plans for front end CQV planning documents along with scheduling. The...
Responsibilities: Provide leadership, strategic planning, direction and implementation of clinical systems for data collection which may include vendor selection, budgeting, resource planning, vendor oversight, EDC build and study timelin...
Roles & Responsibilities : Provide day-to-day technical support for serialization systems (vision systems, printers, scanners, PLCs) in 247 support environment. Troubleshoot and resolve serialization-related issues on packaging lines. E...
Job Summary The CVS Lead is responsible for leading Computer System Validation activities for GxP-regulated systems to ensure compliance with global regulatory standards. The role involves managing validation lifecycle activities, coordina...