- job summary: We are seeking a skilled Validation Engineer to lead validation efforts for a new drug delivery site. This role involves protocol development and execution, audit support, validation assessments, and analyst training, all under limited to no supervision. The ideal candidate will have a strong background in GMP compliance, regulatory standards, and validation processes within the pharmaceutical or medical device industry. Schedule/Shift: 1stjob summary: We are seeking a skilled Validation Engineer to lead validation efforts for a new drug delivery site. This role involves protocol development and execution, audit support, validation assessments, and analyst training, all under limited to no supervision. The ideal candidate will have a strong background in GMP compliance, regulatory standards, and validation processes within the pharmaceutical or medical device industry. Schedule/Shift: 1st
- job summary: The Sr. Clinical Trial Manager (CTM) is responsible for the overall management and oversight of assigned clinical trials and clinical research. The Sr. CTM will be a key contributor to develop study-related documents and create standards and guidelines for clinical research studies and programs ensuring adherence to standard operating procedures, International Conference on Harmonisation/ Good Clinical Practice (ICH-GCP), and FDA regulations.job summary: The Sr. Clinical Trial Manager (CTM) is responsible for the overall management and oversight of assigned clinical trials and clinical research. The Sr. CTM will be a key contributor to develop study-related documents and create standards and guidelines for clinical research studies and programs ensuring adherence to standard operating procedures, International Conference on Harmonisation/ Good Clinical Practice (ICH-GCP), and FDA regulations.
