Chroma Color is hiring directly. Chroma Color Corporation is a technology-leading specialty color concentrate and color master batch supplier. Chroma Color delivers critical aesthetics, technical innovations, and sustainable solutions to plastics processors and brand owners. Having made nine acquisitions Chroma Color’s growth strategy includes robust organic and inorganic growth. Chroma Color’s extensive technical leadership and manufacturing exp...
The Regulatory Associate will exemplify excellent technical writing skills and develop productive working relationships with Manufacturing, Quality, Engineering, and client teams. The Associate will demonstrate exceptional attention to detail and the ability to synthesize complex technical information into regulatory documents that meet FDA, EMA, JP, and other global regulatory authority expectations. The Associate will thrive in a collaborative ...
At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and o...
Location. This position will be located at the Princeton, NJ US Headquarters site. Our Sandoz flexible hybrid working approach allows US office-based employees to work up to 50% of their monthly workday remotely. This role will not have the ability to be located remotely. Preference will be given to local candidates not requiring relocation. U.S. Work visa sponsorship not available for this role. Must have U.S. work authorization. Major Accountab...
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Job Title: Regulatory Associate. Job Description. As a Regulatory Documentation Associate, you will be responsible for organizing compliance documents to support regulatory activities, ensuring federal and state compliance related to the storage, sale, and distribution of FDA-regulated pharmaceuticals. You will work under direct supervision to manage and disseminate important documentation and assist in product releases using regulatory software....
At K2 Medical Research, a privately-owned clinical research facility in the greater Orlando and Central Florida area, we specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. We are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research ...
At K2 Medical Research, a privately-owned clinical research facility in the greater Orlando and Central Florida area, we specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. We are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research ...
Job Title: Regulatory Documentation Associate. Job Description. We are seeking a detail-oriented and organized Regulatory Documentation Associate. Under direct supervision, you will be responsible for organizing compliance documents that aid in planning and executing regulatory activities. The primary goal is to ensure federal and state compliance related to the storage, sale, and distribution of FDA-regulated pharmaceuticals. This role is ideal ...