Job-ID31668236Reference25-04726 Responsibilities: The delivery of regulatory guidance to project teams and external partners is a key activity that assists the company in achieving its business goals. The incumbent will serve as a member of the Global Regulatory department. Serve as the regulatory core team lead and provide active and ongoing regulatory guidance to project teams Responsible for providing guidance to ensure that all regulatory submissions are planned, communicated, and performed per regulatory and business requirements. In addition, this position serves as a subject matter expert on various regulations, coordinating regulatory issue resolution through the use of internal resources, regulatory agencies, and outside consultants as needed. Document regulatory strategies for product submissions. Facilitate and prepare U.S. regulatory Pre-Submission documents for Next Generation Sequencing and/or PCR assays Facilitate FDA pre-submission meetings Prepare U.S. regulatory submissions (PMA, PMA supplement, and 510(k)) for Next Generation Sequencing and/or PCR assays Support EU representatives in their creation of CE/IVD Technical Files Support global regulatory registration representatives for product registration activities Perform regulatory assessment of new and changed products. Stay on top of new or revised regulations, guidelines, points to consider, compliance guides, inspection reports, journals, meetings, etc. Conduct training and/or communicate appropriate materials, as needed, to improve the team's knowledge of working in a regulated environment. Participate in business meetings with potential new external partners. Assist the Regulatory department in updating, improving, and crafting internal policies and procedures. Requirements: B.Sc. or equivalent experience in Biology, Chemistry, bioengineering, or related science at least 5 years of IVD Regulatory Affairs experience. Hands-on experience with 510(k), PMA, and PMA supplement submissions. Knowledge of regulatory strategy creation, design control, cGMP/Quality Systems, and import/export requirements. Ability to lead multiple projects and meet deadlines. Strong communication and teamwork skills. Capacity to communicate regulations to technical functions within the company. Experience as the RA representative on project core teams.
...room changes, LOA, new admits, discharge, etc. Conducts family and patient education. Qualifications Currently licensed as RN in state One-year prior nursing management experience preferred. Brentwood Place Four provides equal employment...
...Riverside, CA Seeking Entry Level Scribe Gain Experience Working Side-By-Side With Frontline Physicians As part of our Medical Scribe program, you play a vital role in supporting physicians and health care providers while gaining first-hand knowledge and practical...
...Years of Experience: - Development and Support experience on web-based applications using the .NET framework ASP.NET, MVC, .NET... ...compliance in systems. qualifications: - Experience designing, developing, and implementing web-based applications using the .NET...
State of Ohio (Ohio Department of Behavioral Health) seeks a Legal Consultant Attorney 5 in Columbus to support behavioral health policy and legal affairs. The role requires active Ohio Bar admission and licensed practice with at least 18 months of attorney experience,...
...Executive HousekeeperManage housekeeping operations in accordance with established guest service, quality and sustainability standards.Potential Career PathArea Executive Housekeeper Assistant General Manager General ManagerEssential Job FunctionsInterview, select...