Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software as a medical device, and de novo devices). The role includes obtaining and maintaining regulatory approvals, supporting quality assurance, and ensuring adherence to regulatory requirements.
...throughout the product lifecycle. With expertise in design, manufacturing, testing, and project management, Segula helps businesses... ...and results-driven Manufacturing Supervisor to oversee the assembly and integration of complex systems and components. This role...
...Job Description Job Description Happy people. Healthy pets. At CityVet, we believe healthy pets start with happy people. It is important that our vet-led clinics are filled with smiling faces and compassionate pet people, and each of our employees play a vital...
...Job Description Host Healthcare is seeking a travel nurse RN PACU - Post Anesthesia Care for a travel nursing job in Saginaw, Michigan. Job Description & Requirements ~ Specialty: PACU - Post Anesthesia Care ~ Discipline: RN ~ Start Date: 11/04/2025~ Duration...
...Job Description Job Description Compensation: based upon experience employment type: full-time/part-Time 1. Dental Receptionist - FULL TIME/PART TIME Our quality oriented dental practice is seeking a bright, enthusiastic, non-smoking, multi-talented individual...
...a 6-month promotion fast-track your career with us! Performance-based bonuses to reward your hard work Employee discounts on pet grooming services Paid time off to relax and recharge Team-building events a chance to connect, unwind, and enjoy some fun together...