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!
...Office Receptionist/Administrative Assistant who has effective communication skills and enjoys working as part of a team. Logical thinker,... ...department and to other departments as necessary Manage corporate incoming emails and website. Accounts Payable for vendor services...
...top jobs with the nation's top schools. Were partnering with a school district in Middlesex County, MA to hire a dedicated Program Nurse (RN). This role is a full-time, 35 hours/week assignment starting ASAP and involves supporting adults with intellectual and developmental...
...methodologies to ensure our clients success. One of our clients, the Appalachian Regional Commission, is looking for a Grants Management Specialist. Organization Overview: The Appalachian Regional Commission (ARC) is an economic development entity of the federal...
...Data Entry Specialist Needed in Southlake! Plaza Premium Group Southlake, Texas 76092*In-office position here in our beautiful Southlake Office. 4 days a week in office, + a work from home day* Plaza Premium Group is the global leader in airport lounges and...
...career advancement: start in customer service evolve into inside sales, and possibly into broader management roles as leadership retires in the next 25 years. If you're energized by customer interaction, order management, and the opportunity to grow into sales and...