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!
BHE GT&S JOB DESCRIPTION BHE GT&S has an exciting opportunity as a Gas Controller I/Gas Controller II or Senior Gas Controller at our Greystone location in Columbia SC. RESPONSIBILITIES Operates natural gas pipeline system to maintain a reliable energy supply...
...Transportation Manager, Logistics, Upstream/Downstream, Supply Chain Davenport, IA. OR Pittsburgh, PA. OR Alcoa, TN. OR Lancaster, PA. Relocation Offered: YES Competitive Salary [about $105K] Plus Bonus, Full Benefits, World Class, Global Job Description...
...potential and current clients, ensuring that services provided are appropriate and meet their healthcare requirements. Primary Duties include but are not limited to: Develop and update comprehensive care plans. Provide staff training, ensure accurate...
...Job Description Spectrum Healthcare Resources has a potential need for LPN Care Coordinator These will be completely remote positions, working entirely from the Nurse's home. Coordinates transitions of care for TRICARE beneficiaries. Care Coordinators receive...
...About this Position: Job Title: Security Analyst General Duties and Responsibilities: Perform detailed architectural reviews and risk analysis of security related requests in order to make sound decision making recommendations, such as: Network Design and...