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!
...flexible) Type : Temp to Hire Responsibilities Receive and prepare raw, in-process, and finished product samples for microbiological analysis. Maintain accurate and legible documentation Practice Good Laboratory Practices (GLPs) Review all test results...
...all students. Performing duties as requested by the Special Education Administrator. **Incentive Stipend for Bilingual SLP BENEFITS: The City of Lynn offers comprehensive and competitive health and dental benefits; Harvard Pilgrim PPO/HMO, Altus...
...Pittsburgh area and beyond. The company's mission is to provide objective and timely financial advice to help clients build, manage, protect, and transfer their wealth. Role Description This is a part-time on-site role for a Client Service Associate located in Pittsburgh...
Job Description: Preferred experience in the assessment and preparation of manufacturing sites for Pre-Approval inspections by Regulatory agencies for new products. Reporting to the Quality Assurance Organization, will independently manage project assignments. ...
...Our client, a leading innovator in wholesale distribution, is seeking a highly reliable and motivated Delivery Driver to join their growing team. This role is vital in ensuring the seamless delivery of products to local businesses across the Greater Los Angeles area....