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!
...Are you an experienced UX/UI Designer with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced UX/UI Designer to work at their company in Maple Grove, MN. Position Summary: Seeking an exceptional,...
Description of the role:The UPS Store #6691 in Plano, TX is seeking a Part-Time Center Associate to join their team. This is a customer-facing role that involves providing exceptional service to customers and supporting the daily operations of the store.Responsibilities...
...Local candidates preferred) Project Type: Data Center Construction Position Overview We are seeking an Environmental, Health & Safety (EHS) Coordinator to support a large-scale data center construction project in Gainesville, VA . This role is ideal for...
Brand & Creative Manager Crown Display | Full-Time | On-Site About Us Crown Display is a fast-growing leader in partyware and consumer goods, offering 2,500+ SKUs across major retailers, online marketplaces, and our own vertically integrated operations. Were ...
...Location: On Site - Mcpherson, Kansas Salary: $25-$30/hr Skills: Medical Coding, ICD/CPT/HCPCS, Rural Health Clinic Billing, Clinical Knowledge, Coding Compliance About the Company / Opportunity: Join a respected organization in the hospitals and health...