Company Overview At FUJIFILM Biotechnologies, we’re leading the charge in advancing tomorrow’s medicines. If you want to be a part of life-impacting projects alongside today’s most innovative biopharmaceutical companies, FUJIFILM Biotechnologies could be the right place
This is a full time on-site position with M-F business hours About This Role The Sr. Associate I is responsible for the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen
Vulcan Elements is manufacturing American rare-earth permanent magnets for a secure, resilient future. With a focus on national security and economic resiliency, we serve critical industries such as defense, aerospace, and automotive powering a high-technology future.
GMP Compliance Investigator - Equipment and Facilities - Marcus Center for Cellular Cures School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nations top medical schools. Ranked sixth among
QA Operations Head Join Novartis as our QA Operations Head and play a pivotal role in ensuring patients receive high-quality medicines that meet the highest standards of safety, compliance, and reliability. This is an opportunity to
Documentation Area Specialist I Support daily GMP manufacturing operations by performing production sampling, managing batch documentation and GLIMS activities, and coordinating with cross-functional stakeholders to ensure accurate, timely, and compliant execution of manufacturing processes that enable product
This job is with Biogen, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. This is a full time on-site
Sample Management Coordinator Support daily GMP manufacturing operations by performing production sampling, managing batch documentation and GLIMS activities, and coordinating with cross-functional stakeholders to ensure accurate, timely, and compliant execution of manufacturing processes that enable product quality
GMP Manufacturing Support Specialist Job Title: Documentation Area Specialist Location: Durham, NC Duration: 6 months (Temporary) Schedule: Onsite, MondayFriday (5 days/week) Pay Rate: $33.69 Top Skills Attention to Detail Team Player/Positive Attitude Computer Literacy Purpose Support
Clinical Supply Chain Manager, Strategic Development We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients
QA Manufacturing Specialist II (Nights) This is a night shift opportunity that follows a 2-2-3 schedule. The QA Manufacturing Specialist II (Nights) is responsible for ensuring raw materials, products, processes, facilities, documentation, and systems conform to