We are NOT accepting resumes from recruitment agencies or search firms. About Instylla. Instylla, Inc. is a privately held medical device company based in Bedford, MA, focused on developing novel resorbable embolic agents to advance interventional radiology, with initial clinical applications in interventional oncology. Instylla was founded in 2017 by Incept LLC and is funded by several leading venture capital groups. The company’s flagship produ...
Regulatory Affairs Coordinator I. Location. Irvine, CA. Duration. 1 year contract. Education Requirement. Bachelor’s degree minimum. Experience. Regulatory support experience. international submission support preferred. Overview. The Regulatory Affairs Coordinator plays a key role in supporting the Surgical Vision regulatory organization by managing documentation, preparing routine submissions, and maintaining high-quality records across global r...
Manage all label change and creation processes for products, such as changes from new products, new package sizes, reformulation, new suppliers, new regulatory requirements, and marketing initiatives. Manage all Kosher Schedule A and B approval and documentation processes. Review and update raw material and ingredient specifications and other documents as needed for food safety risk, regulatory conformity, impact to claims, and supplier/ raw mate...
Job Description. The successful candidate will be responsible for generating and validating official technical documents and ensuring compliance with both domestic and international regulatory requirements for flavors and ingredient systems. This position involves conducting risk assessments, reviewing product labels, collaborating with cross-functional teams, and staying updated on regulatory changes. Responsibilities. Generate and validate offi...
Description. The Regulatory Specialist is responsible for supporting the Regulatory Affairs department in maintaining efficient and compliant business processes. The Specialist partners with cross-functional teams to gather, organize, and present data required for global product registrations. They prepare, submit, oversee regulatory documentation and ensure accurate information management, file maintenance, and coordination across multiple depar...
Regulatory Specialist, Quality Management. Full Time, 80 Hours Per Pay Period, Day Shift. LeConte Medical Center Overview. LeConte Medical Center is a part of Covenant Health, our region’s top-performing healthcare network and is a 79-bed community hospital located in the heart of Sevier County. We’re a full-service, not-for-profit hospital delivering modern medicine and compassionate care to the growing Sevier County community. LeConte offers a ...
Job Title. Project Coordinator (Regulatory Compliance). Client Location. ONSITE. Foster City, CA. Pay Comments. W2. Minimum Pay (per hour). 49.00. Maximum Pay (per hour). 53.85. Hours. Full-time. Duration. Approx. 6 Month Assignment. We are seeking a detail-oriented compliance professional to own the end-to-end process for vehicle registration, permitting, and ongoing compliance obligations. This role operates at the intersection of legal, operat...
About 10x Health System. 10X Health System is a pioneering company at the forefront of the health and wellness industry, dedicated to revolutionizing the way individuals approach their personal health and well-being. With a philosophy rooted in the principle that optimal health is the foundation for a life lived to the fullest, 10X Health provides cutting-edge solutions and personalized health plans designed to empower individuals to achieve and ...
Join us at Entrust . At Entrust, we’re shaping the future of identity centric security solutions. From our comprehensive portfolio of solutions to our flexible, global workplace, we empower careers, foster collaboration, and build solutions that help keep the world moving safely. . . Get to Know Us . Headquartered in Minnesota, Entrust is an industry leader in identity-centric security solutions, serving over 150 countries with cutting-edge, sc...
Job Title: Regulatory Specialist. Job Description. As a Regulatory Specialist, you will be responsible for processing all initial regulatory documents for submission to Pharmaceutical Sponsors and Institutional Review Boards (IRB). You will also prepare and process required regulatory documentation through the IRB, CTSRMC, FDA, and other applicable regulatory review committees. This role involves working with pharmaceutical companies, contract re...
Job Title: Regulatory Specialist. Job Description. As a Regulatory Specialist, you will be responsible for processing all initial regulatory documents for submission to Pharmaceutical Sponsors and Institutional Review Boards (IRB). You will also prepare and process required regulatory documentation through the IRB, CTSRMC, FDA, and other applicable regulatory review committees. This role involves working with pharmaceutical companies, contract re...
