WebFocus Developer

Join us at StemXpert as a WebFocus Developer where your expertise will contribute to innovative data solutions. You'll work in a dynamic environment that values creativity and collaboration, developing applications that enhance data visualization and efficiency.

Join our dynamic team at 360itprofessionals as a LAMP Developer, where you'll have the opportunity to work on exciting projects using your expertise in Linux, Apache, MySQL, and PHP. We are looking for a passionate developer who thrives in a collaborative environment and is eager to learn and grow with us.

We are seeking a talented Contract Development Engineer to join our innovative team at Integrated Resources Inc. In this role, you will collaborate with cross-functional teams to design, develop, and implement engineering solutions that meet the needs of our clients. This position is ideal for motivated individuals who thrive in fast-paced environments and are eager to contribute to exciting projects.

Join our dynamic Consumables Research & Development team as a Senior Development Engineer, where you will play a crucial role in the Design Verification of our innovative Consumables products.In accordance with Design Control procedures, you will establish testing protocols to ensure that product designs fulfill all specified requirements. Your responsibilities will include crafting engineering protocols, performing data analysis, and generating comprehensive reports.

Join Northwestern Medicine as a dedicated Administrative Coordinator in Nursing Administration and Professional Development. This part-time position focuses on supporting nursing leadership and enhancing professional development initiatives within our organization. You will play a crucial role in coordinating activities, managing schedules, and ensuring effective communication among various departments.

Join our dynamic team as a Regulatory Affairs Manager, where you will play a pivotal role in leading our project development teams primarily focused on drug products. Your expertise will guide our efforts in navigating regulatory compliance, ensuring alignment with FDA requirements, and optimizing clinical study designs.Act as the chief regulatory affairs representative on project teams, providing strategic regulatory oversight.Offer thorough guidance on compliance matters, including timing, logistics, and operational recommendations for product development.Develop effective regulatory submission strategies in alignment with product development objectives.Serve as the primary liaison with the FDA and other health authorities for assigned Investigational New Drug (IND) and New Drug Applications (NDA) projects. Prepare and submit IND and NDA applications, along with amendments and supplements.

Develop and validate sophisticated analytical methods tailored for the evaluation of large molecule products. Facilitate global method transfer and troubleshoot any arising issues. Analyze experimental data, and compile comprehensive reports and presentations.Essential Qualifications: Proven expertise in cell culture, immunoassay, and bioassay development is a must.Exemplary documentation skills are required.Preferred Skills: Familiarity with flow cytometry, Biacore, cell signaling, laboratory automation, and Design of Experiments (DOE) is advantageous.Design and qualify precise ELISA, CRBA, and cell-based potency assays for large molecule product analysis. Assist in global validation, method transfers, and troubleshooting of bioassays. Conduct characterization sample testing, perform statistical data analysis, summarize assay results, and maintain electronic notebooks and reports.