3 assistant operations manager jobs found

Merck Job Description The Developmental and Reproductive Toxicology (DART) group within Nonclinical Drug Safety (NDS), is seeking a highly motivated person with strong technical skills and diligence to conduct in vivo studies as part of a collaborative team supporting drug development programs. The successful candidate will perform in vivo administration of compound, data collection, cesarean sections with fetal examination, and necropsies under limited supervision. The position requires the ability to maintain neat, concise, and accurate records, along with good oral communication skills. The successful candidate will also train and work cross-functionally, assisting other areas within NDS. This position is for a 5-day work week, including coverage of weekends and Holidays on a rotational basis. Specific responsibilities include but are not limited to: Perform assigned tasks that include dose administration by various routes; recording of body weights, food...

Merck Job Description PDMB provides data-driven operations and automation support to regulated bioanalytical laboratories. We combine laboratory domain knowledge, robotic work cells, and modern data platforms to ensure reliable, compliant, and continuously improving lab operations. You'll join a multidisciplinary team partnering with lab scientists, automation engineers, IT, Clinical, and QA, to turn operational and scientific data into trusted insights. The PDMB Regulated Bioanalytics Department is seeking a Data Management Associate to join our LIMS & Data Management group.This role will support work across groups within the Regulated Bioanalytics Department, including work at our Company's new state-of-the-art GxP lab facility in West Point, PA. At this new facility, we will combine the power of innovative robotics, IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated...

Merck Job Description Position Overview - Basic Functions & Responsibility The Global Clinical Supply (GCS) organization is within our Research & Development Division and is accountable for managing the 'end-to-end' integrated clinical supply chain across our Research & Development Division portfolio to enable the execution of any clinical trial using our Company's assets. GCS supports more than 300 Phase I-IV clinical trials run in-house, 400+ outsourced or run by partners as well as our Company's ISS clinical trials (300+). GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites across more than 60+ countries, all in accordance with US and WW regulations, company policies and Standard Operating Procedures. The Director, Continuous Improvement, will lead continuous improvement (CI) activities within the organization and functional areas, supporting CI culture. The role will oversee both...