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!
OverviewOur YOU FIRST PhilosophyIn addition to no night shifts, ever and our fully chef-curated menu, our #1 priority has always been our people. We care about our customers, and we care about you! That's where our YOU FIRST culture begins - each day, we put our employees...
...Bachelors degree in Engineering or similar technical field ~3+ years of relevant experience working with OEM suppliers and manufacturing operations building complex hardware/software systems ~3+ years experience in engineering, manufacturing, or quality within the...
Job Overview TheAgent Talent Relationsrole focuses on identifying, attracting, and onboarding high-quality real estate agents who align with the brokerages culture and growth goals across South-Central Pennsylvania. This position builds strong relationships with productive...
...with the nations schools. Were partnering with a school district in Providence County, RI to hire a dedicated Licensed Practical Nurse (LPN) or Registered Nurse (RN) to support a kindergarten student during daily transportation. This role involves riding the school...
...:00pm - 10:30pm (Full Time, Swing) What Youll Make $20.60 - $21.86 per hour DOE/Credentials. An additional $3.00 per hour night shift differential will apply during the work hours of 10:00pm - 6:00am. Additional 5% Language Differential offered for Bilingual...