tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA...Description The Senior Clinical Research Coordinator (Senior CRC) contributes to the overall operational management...
Human Factors & User Experience team in the Drug Delivery Systems (DDS) group as part of the broader Drug Product... across various stages of development within the DDS group. Responsibilities include authoring Human Factors plans and protocols...
insurance, and group legal insurance. Employees may be eligible to participate in the Company’s consolidated retirement plan... across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health...
Position Overview: The Sales Specialist, Diagnostic Oncology, in the Invitro Diagnostics Division, is responsible... for identifying, prioritizing, and establishing relationships with Key Accounts and Opinion Leaders within the Liver/Hepatology...
, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible... across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health...
13485 and FDA QSR preferred;scientific molding knowledge a plus. Comfortable spending real time on the shop floor... — and you'll be the go-to technical expert for the production floor. What you'll do Own the manufacturing processes...
Lugar:
Simsbury, CT | 22/08/2026 00:08:48 AM | Salario: S/. No Especificado | Empresa:
GPAC Station, TX. Company Overview: The work we do at FUJIFILM Biotechnologies Texas has never been more important...—and we are looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. From developing the...
. This position plays a critical role in the growth and development of thegroup and contributes to organizational effectiveness... administration Solid understanding of the drug development process, including Good Clinical Practices (GCPs) and FDA Code of Federal...
, Radiation Safety, applicable FDA and pharmacy laws, DOT, and internal policies and interpretations Manages small group..., and environmental commitment. Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals...
generation, and scientific communication across the product lifecycle to support regulatory approvals, indication expansions..., and Medical Affairs initiatives. Responsibilities Lead the scientific design, development, and oversight of pivotal, post...
Lugar:
Valencia, CA | 22/08/2026 00:08:06 AM | Salario: S/. No Especificado | Empresa:
Sonova