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!
...Our client, a Junior's apparel manufacturing company, is seeking an Assistant Designer to support their growing team. Key Responsibilities: Conduct research on current fashion trends, fabric innovations, and market demands to inform design decisions and ensure relevance...
...Compensation: $,65000$75,000 annually Travel: Moderate travel for customer visits, trade shows, and industry events. Benefits:... ... Coordinate internally with operations, inventory, and service teams to ensure customer requirements are fulfilled Conduct...
Description: Summary: Submits physician orders and coordinates schedules with the needs of the facilities and ordering physicians by performing the following duties. Qualifications: Prior experience not required but preferred. Ability to multitask, critically think...
...Level III), Vascular, EP, Thoracic, OB, Orthopedics, Urology, General, GYN, and GI (no Peds or ENT). One... ...bonus up to $75,000 and relocation assistance available. ~ Immediate 8 weeks time... ...center, an urgent care center, and 46 physician practices in the state. About...
...At KR Solar , we dont just sell solar panelswe sell freedom . Freedom from high bills. Freedom from playing defense against rising... ...(or equivalent experience) Proven work experience in solar sales, with at least 2 years in a sales management role In-depth...