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!
About Us Since 2002, Luckyscent has been the playground for perfume lovers who refuse to smell like everyone else. We scout the globe for niche, rare, rule-breaking fragrances and bring them to our community through our online store and our boutiques in NYC, Hollywood...
Job Title: Receptionist/ Administrative Assistant Location: East Rutherford, NJ Pay Rate: $24-$26/hr Start Date: ASAP Duration: Through end of February (potential to extend)5 days on site Overview We are seeking a highly organized Receptionist/ Admin...
...English language. Ability to work overtime and late hours on short notice. Available to work non-traditional schedule, including nights and weekends. Must pass a written exam. A commitment to diversity, equity, accessibility, and inclusion. Physical...
Pride Health is hiring a Special Investigative Unit Investigator for one of its clients in Michigan. This is a 12-week contract with a possible extension, with competitive pay and benefits. This position is remote, but candidates MUST be in Eastern or Central ...
...resolve technical issues within the desktop computing environment. Prepares customers to use hardware and software by conducting training where necessary. Documents new and existing procedures and processes within technician knowledgebase. What You Bring to...