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!
...with potential extension or conversion) Target start date : Jan 5,2026 Worksite:... ...PA Job Summary MGT is a national leader in public sector management consulting and... ...Technical Evaluation Round 2 : Client Teams interview (23 panel members) Round 3:...
...PhD or PsyD in Psychology required. Active California license as a psychologist required. Required experience in: Testing... ...Excellent benefits: Details to follow90% employer-paid health insurance Low-cost dependent coverage includes domestic partners....
...requirements. Other duties as assigned. Qualifications High School Diploma or equivalent required. No prior experience necessary; training provided. Ability to work independently and with attention to detail. Basic computer skills (Microsoft Word and...
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Join a global community of talented professionals to shape the future of AI. Earn up to $15 USD/hr and additional rewards based on quality of submission. Outlier is committed to improving the intelligence & safety of AI models. Owned and operated by Scale AI , weve ...