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This role is to fill in for 4 months for a Clients’ Manager who is going on a Maternity leave. Minimum of 5 years of relevant experience Proven experience with regulatory submissions, including IND and CTAs Strong background in reviewing and editing regulatory affairs documents At least a Bachelor’s degree (with a heavy emphasis on hands-on experience) Additionally, the position will involve a panel interview as part of the selection process We are seeking a Manager, Global Regulatory Affairs, to work closely with the Global Regulatory Lead (GRL) for a given program(s).
The Division is seeking a strong Systems Administrator to assist with Red Hat Linux systems. The candidate will support Linux and windows server and desktop environments in the unclassified, collateral secret and higher program spaces.
We are looking for a meticulous sterile processing technician to be responsible for the sterilization and cleaning of medical equipment, instruments, and supplies. The sterile processing technician's responsibilities include retrieving contaminated supplies and delivering sterile supplies, maintaining inventory, and preparing sterile instrument trays for surgeries, examinations, and procedures
This position involves conducting polymer synthesis, characterizing products, and supporting process improvements while adhering to safety and quality standards. The role requires strong lab skills, effective communication, and teamwork to contribute to research and production efforts.
Performs eCTD submission management across Biogen's product portfolio to Health Authorities for global development and lifecycle management submissions. The Regulatory Ops. Manager is responsible for the coordination of all publishing deliverables, in line with the strategic direction of their assigned programs/products. Oversee outsourced publishing deliverables on a day-to-day basis to ensure successful execution of operational activities for assigned products.
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