: Bachelor's degree in engineering, LifeSciences, or a related field. 5+years of relevant experience in validation...
Job Description: Performs routine production functions including filling, utility operations, packing, packaging, assembling, labeling and inspecting under general supervision. Maintains accurate records and logs in accordance with FDA (...
Job Summary: Quality Assurance Engineer responsible for providing design assurance support for new product development and on-market medical devices. The role focuses on facilitating design controls, ensuring regulatory compliance, supp...
most important research questions across clinical development, market access, and commercial use cases for our lifesciences partners...., PhD, ScD, DrPH) in Biostatistics/Statistics, Data Science, Bioinformatics, Biological Sciences, Public Health, Math...
Job Description: Responsibility for the Quality and Compliance of process development and manufacturing of implantable ( Class III) Cardiac and Neuromodulation medical device related products. Initial scope of work may be focused on Inspec...
Strong understanding of medical device product life cycle and regulatory requirements In-depth knowledge of ISO 13485, FDA regulations...
Job Summary: Quality Engineer responsible for supporting manufacturing operations by managing nonconformances and CAPA activities, assisting inspection teams, and conducting investigations related to field corrective actions and risk eval...
Science, LifeSciences, or related field. Advanced degree (Master's) preferred but not mandatory. Additional certifications...
+years of experience with System Development Life Cycle (SDLC). 7+years of experience in Computer System Validation...
Job Description: The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing statistical programming activities across multiple clinical trials and therapeutic areas. The role oversees external CRO partner...