Job Description: We are seeking an experienced Project Manager with a strong background in the medical device industry to support cross-functional initiatives across Operations, Manufacturing, and Supply Chain. The ideal candidate will ha...
Job Description: We are looking for an experienced Senior Lab Instrument Support Engineer (Equipment Validation Engineer) to support GxP-regulated analytical laboratories across NJ and PA. This is a hands-on, onsite role for a professiona...
Responsibilities: Serve as the main contact for service-related inquiries from recruitment, managers, employees, and other HR team members. Ensure the complete resolution of HR requests, including tracking and tracing. Offer outstanding...
Job Description: This position is responsible for the successful implementation and coordination of equipment and facilities validation programs in compliance to cGMPs, FDA requirements and company policy. Development and execution of equi...
Job Description: Equipment Validation Specialist exists to ensure all critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters and global regulatory guidelines. The role provi...
Job Description: We are currently seeking a highly motivated and passionate scientist to join the Exploratory Biologics group within the Immunology Discovery Department in Cambridge, MA. The successful candidate will contribute to the disc...
Job Description: The Quantitative, Translational ADME Sciences (QTAS) department at client is seeking a highly motivated and energetic bioanalytical scientist to join the biologics bioanalysis, characterization, and proteomics (BBCP) group...
Job Description: This position is responsible for the successful implementation and coordination of equipment and facilities validation programs in compliance to cGMPs, FDA requirements and company policy. Development and execution of equi...
Responsibilities: Lead the development, validation, and documentation of CDISC-compliant SDTM and ADaM datasets for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings, and f...
Responsibilities: The delivery of regulatory guidance to project teams and external partners is a key activity that assists the company in achieving its business goals. The incumbent will serve as a member of the Global Regulatory departm...