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!
...Were seeking an Ammonia Refrigeration Technician who can independently maintain, troubleshoot, and repair industrial ammonia systems across two facilities. Responsibilities: Inspect, test, troubleshoot, and repair ammonia refrigeration systems Monitor/control...
Company Description Boyd Gaming Corporation has been successful in gaming jurisdiction in which we operate in the United States and is one of the premier casino entertainment companies in the United States. Never content to rest upon our successes, we will continue ...
...Immediate need for a talented Registered Nurse (RN) Operating Room Circulator . This is a Fulltime opportunity with long-term potential and is located in Marietta, Georgia (Onsite) . Please review the job description below and contact me ASAP if you are interested...
...POSITION PURPOSE AND EXPECTATION: The HR System Administrator serves as the primary administrator and subject matter expert for Lovisa's ADP Workforce Now platform, ensuring accurate and efficient system operation across all employee lifecycle stages. This dedicated...
...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:...