's or master's degree in Immunology, Cell Biology or a related Biological Sciences field, with 3-5 years of relevant hands...
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 professional...
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...
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...
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...
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: The Quantitative, Translational ADME Sciences (QTAS) department at client is seeking a highly...
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...
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...
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...