Are you a Regulatory Affairs professional looking to work independently and take ownership of the writing of CMC sections of DMF, BLA, and NDA submissions? Have you supported full product development activities from pre-clinical/clinical to FDA submissions? Are you interested in helping a company expand their client base in new countries? Do you have experience independently writing CMC sections of global regulatory submissions? This position could be for you!
If you're interested in a Lead Regulatory Affairs Specialist position with a well established pharmaceutical company in Madison, Wisconsin, apply here for more details!
...GHR Education has an exciting opportunity for an Occupational Therapist (OT) at a school near you! Occupational Therapist (OT) Job Details: ~*Interviewing now for the 2025-26 school year!*~*Full-time and part-time available*~ Pay: $60/hr (W2 weekly pay + benefits...
...Pride Health is hiring RN OR to support our clients medical facility based in Columbus, Ohio. This contract opportunity is a great... ...Experience Minimum 2 years of Operating Room RN experience Prior travel experience required Strong circulate and scrub experience...
...The Junior Merchandise Planner holds responsibility for assisting with the development and execution of the product plans from merchandise planning through the merchandise allocation stage. This role is a starting point on the planning team, inclusive of a development...
...Central Health Management is seeking a qualified, licensed Nurse Practitioner with experience in primary care for a part-time role in the Virginia Beach/Hampton... ...practice care management. The role involves some travel in the area and is compensated accordingly. The schedule...
...openings for dependable Class C Special Delivery Truck Drivers to safely and efficiently operate a... ...products (meats, produce, frozen foods, groceries, dry goods, supplies, etc.) to... ...why Sysco is at the heart of food and service. AFFIRMATIVE ACTION STATEMENT:...