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!
...bonuses!!- Be Home Daily ' Say goodbye to long-haul trips!- Uniforms Provided ' Stay comfortable and professional. - Annual Safe Driver Awards ' We recognize and reward safe driving. - 90% No-Touch Freight ' Easy delivery, palletized product. - Fun Incentives '...
...Manager. Compensation is hourly commensurate with skills and experience and is reviewed annually. Clear advancement opportunities exist... ...Plain Electrics modeling, drawing standards, and CAD and BIM software platforms. Work on multiple projects throughout the workday...
...: ~ Bachelors degree in finance, accounting, real estate, or related field ~2+ years of experience in asset management, affordable housing, accounting, or development ~ Strong Excel and financial analysis skills ~ Familiarity with LIHTC/affordable housing preferred...
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...electronic and paper claim submissions to insurance payers. Coordinates required information... ...supportive documentation. Education, License & Cert: High school diploma required;... ...confidentiality related to patient health information in accordance with HIPAA regulations...