Summary: The Manager, Quality Systems is responsible for providing end-to-end quality assurance oversight across designated manufacturing operations, which may include pharmaceutical products, medical devices, cosmetics, biologics, and com...
Job description: The Biologics CMC Developability (BCD) group sits at the interface of discovery and development. The core role of BCD is to deliver meaningful and actionable data to support the selection of candidate molecules to progress...
Job description: Collects environmental and utility samples for microbiological and chemical testing. Performs microbiological testing on water and swabs. Responsibilities: Implements, maintains, and makes changes to create global solu...
Job Description: The Global Material Review Project Manager is responsible for managing the end-to-end review and approval process of global promotional materials within a highly regulated pharmaceutical environment. This role leads cross-...
Job Description: The Manager, Quality Systems is responsible for providing end-to-end quality assurance oversight across designated manufacturing operations, which may include pharmaceutical products, medical devices, cosmetics, biologics...
Job Description: The Manager, Quality Systems is responsible for providing end-to-end quality assurance oversight across designated manufacturing operations, which may include pharmaceutical products, medical devices, cosmetics, biologics...
Responsibilities: The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Resea...
J ob Description: The Intake Specialist role works to support the Patient Assistance Program (PAP) through providing initial triaging of patient applications, including data entry and coordination of work through the appropriate channels a...
Responsibilities: Accurate and timely registration of adverse event and product quality report from initial receipt to data entry within required timeframes. Performing Quality Review of external provider's reconciliation tasks for Clini...
Job Description: In this role, you will play a vital role in supporting our team of seasoned scientists and engineers, contributing to lab-based projects that drive innovation and excellence within the client. Our team is responsible for p...
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 Description: The Regulatory Affairs Associate will be responsible for managing, authoring, and compiling Chemistry, Manufacturing, and Control (CMC) sections of regulatory submissions for marketed product variations, including Class II...
Job Description: The Epi Forecasting Senior Epidemiologist will serve as a key contributor within the Epidemiology Forecasting Center of Excellence (CoE). In this contractor role, you will design and execute descriptive epidemiologic and p...
Job Description: Laboratory Systems Operations (LSO) group is a key study team partner in the lab engagement process and plays a critical role in supporting Client Clinical Trials. For every Client clinical study, LSO assists with the dev...
Responsibilities: Accurate and timely registration of adverse event and product quality report from initial receipt to data entry within required timeframes. Performing Quality Review of external provider's reconciliation tasks for Clini...
Job Description: Experienced with lab settings for daily support of safety, lab organization and lab upkeep (receiving materials, waste management, etc.). Role requires support of multiple lab areas at multiple sites. Experience with anal...
Job Description: Responsible for supporting Process Chemistry and Engineering operations within the Pharmaceutical Products Group - API at Client Lake County. The Lab Manager will work directly with organizing laboratory spaces, managing c...
The Regulatory Affairs Associate will be responsible for managing, authoring, and compiling Chemistry, Manufacturing, and Control (CMC) sections of regulatory submissions for marketed product variations, including Class III implantable medi...
Job Description: Product Development Science and Technology (PDS&T) is seeking a motivated Scientist to support parenteral drug product process development, scale-up, and technology transfer to commercial manufacturing sites. This role wi...
Responsibilities: The role includes obtaining and maintaining regulatory approvals, supporting quality management system (QMS) objectives, and ensuring adherence to applicable regulatory standards. The Regulatory Affairs position is resp...