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!
...THIS IS A 1-2 MONTH CONTRACT!! We are seeking meticulous, detail-oriented individuals with clerical and data entry experience to join our team as Entry-Level Data Specialists. You will consolidate student records from multiple drives and sources, organize documents into...
...Position Summary We are seeking an experienced and visionary Podcast Showrunner to lead the creative and production process for My Price is My Life . The ideal candidate is a storyteller, producer, and strategist who can oversee the podcast from concept to...
...currently seeks an experienced Part-Time/PRN Psychiatric Registered Nurse for our Home Health patients in Clearfield, PA. Provides... ...& Dental Insurance. ~ Company paid life insurance ~401(k) retirement with a generous company match ~ Company provided web-based...
IMMEDIATELY HIRING Warehouse Order Selectors**NO EXPERIENCE REQUIRED**Hiring immediatelyEarn up to $18.00 per hour including base, overtime, and incentivesIndustry-leading total rewards packageOn-the-job training with career growth opportunitiesNo college degree or...
...Qualifications Minimum of 5 years of experience as a superintendent or foreman in heavy civil construction Background in dam, marine, bridge, or environmental restoration projects Ability to read and interpret construction drawings and technical specifications...