Responsibilities: Develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD Guarantee quality of statistical output produced by external provider, to program tools to support data ...
Responsibilities: Provide leadership, strategic planning, direction and implementation of clinical systems for data collection which may include vendor selection, budgeting, resource planning, vendor oversight, EDC build and study timelin...
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...
Roles & Responsibilities: Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Client procedures and guidelines, the duties and responsibilities for this position are: I d...
Job Summary: The Process Validation Engineer supports medical device manufacturing by developing, executing, and maintaining validated manufacturing and test processes. The role ensures compliance with FDA QSR (21 CFR 820), ISO 13485, a...
Roles & Responsibilities: Plan, lead, and execute the validation efforts for SCADA, Rockwell Factory Talk, PLC's and Ignition Talk Create/write validation documentation (VP/URS/FS/DS/Trace Matrix/Risk Assessment/IQ/OQ/PQ, etc.) for proce...
Summary: As Qualification Specialist in the Equipment Integration team, you are responsible for caring about the GMP requirements. The team is responsible for transferring existing Lab Equipment from Spark Network to Roche Connect Network...
Responsibilities: Support Mechanical Design Optimization Projects: Contribute to projects aimed at improving our engineering and manufacturing processes. Data Collection and Analysis: Collect and process raw data and conduct analysis to ...
Summary: We are seeking a Quality Engineer with experience in the medical device industry to support quality assurance, regulatory compliance, and continuous improvement initiatives. The ideal candidate will have a strong background in FDA...
Job description : We are seeking a Senior Quality Engineer to support process development, manufacturing quality, and compliance for implantable cardiac and neuromodulation medical devices. This role focuses on inspection optimization, p...