PRINCIPAL SCIENTIST, PEPTIDE / BIO-ORGANIC CHEMISTRY This BioPharma is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, endocrine and psychiatric disorders. The company’s diverse portfolio includes FDA-approve
Clinical Stage Pharmaceutical Company is looking for a Senior Manager, Quality Assurance Key Responsibilities * Provide leadership, strategy, and compliance oversight in accordance with Good Manufacturing Practices (GMPs) for internal processes, GMP Service Providers, including but not limited to CMOs, Third Party Vendors, etc. * Responsible for Management and maintenance of the Veeva Quality Docs System, includi
My client is expanding and seeks a Computational Antibody Engineer to develop a computational platform for designing proteins and antibodies. The ideal candidate will take on the following tasks: * Collaborate with team and develop a computational platform for protein and antibody engineering. * Create processes for protein structure determination using AI and other methods. * Develop pipelines for protein dockin
City Planner with AICP Certification (or working towards certification) needed for a growing city in one of the fastest-growing parishes in southeastern Louisiana. In this role you will determine the best way to use the city’s land and resources and assist in guiding the orderly growth and development of the city. The city is centrally located between two major interstates, which contributes to the area’s attractive
My client is expanding and seeks a Director to take on the following tasks: · Serve as a scientific liaison for internal and external partnerships, driving collaborative oncology research. · Direct operations, staff, and core functions, ensuring quality, timeliness, and accuracy. · Manage strategic expansion of the laboratory footprint and services, identifying and implementing processes to enhance efficiency and ut
Quality Control Inspector * A related degree and two plus years of quality inspection experience is required * Swing shift (Five-day, twelve-hour rotating shift with a block of six days off every three weeks) * Pay up to $24 per hour * Must be a United States citizen or Green Card holder * No remote * Full-time * Permanent W-2 employee * Full benefits * No relocation * De Pere, Wisconsin area This full t
Director DMPK (possibility for Senior Director title) Top Tier Pharmaceutical company is expanding their high profile DMPK Team: About the Role: Develops strategic plans and objectives for area of responsibility, including working with Research, Clinical Pharmacology and Bioanalytical colleagues to develop overall Preclinical Pharmacokinetic Strategies for subsequent ratification by project teams. Plays a key role
Our client - a growing Pharmaceutical company located in central NJ - is looking for multiple Analytical Chemists as part of their ongoing expansion. The Analytical Chemists will be tasked with helping to ensure drug product quality and support Submission Batches. They will perform method development, method validation, method transfer and technical investigations (which will involve analyzing data and as well as t
My client is expanding globally and seeks a trained phase 1 clinical trial Pharmacist to grow and lead a group. This person will take on the following tasks: · Review and edit phase 1 protocols and contribute to protocol development. Ensure global compliance with GCP principles and documentation standards. · Create pharmacy manual development, design, and review, including tools to communicate the scope and the valu
Position Overview: Serves as the lead for Vaccine development strategy and execution of clinical trials. This role will be responsible for designing and executing clinical studies, helping to build the clinical development plan and execute the plan for new vaccine assets. Provides input on local risk management activities and medical oversight of all clinical trial related activities, adhering to GCP/GMP standards
