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Leading the design and implementation of digital systems for the production of Individualized Neoantigen Therapies. Collaborating with various teams to optimize processes and support automation in pharmaceutical/biotechnology manufacturing and lab systems.

Seeking a Scientist with a strong background in Analytical Chemistry to work on stability studies for mRNA-Lipid Nanoparticles based vaccines and therapeutics. Responsibilities include study designs, data analysis, technical leadership, and documentation for regulatory submissions. Must have 5-8 years of biotech or pharma industry experience.

Seeking an accomplished Principal Statistician to provide strategic statistical guidance and leadership. Responsibilities include partnering with cross-functional teams, mentoring junior team members, and advancing knowledge in relevant CMC topics.

Managing day-to-day activities in the laboratory, ensuring compliance with regulations, maintaining inventory, documenting protocols, training personnel, managing budget, supporting operational excellence initiatives, collaborating with cross-functional teams, and fostering a culture of collaboration and continuous improvement.

Engineer I role at Moderna's Process Development team focusing on mRNA and lipid nanoparticle technologies. Responsibilities include designing and executing experiments, defining critical parameters, and analyzing process performance. Requires BS/MS in relevant field, hands-on experience with various unit operations, knowledge of DoE and cGMP, and ability to provide technical support for commercial manufacturing processes.

Seeking an Associate Systems Engineer to support the Validation, Delivery and Administration of GxP laboratory benchtop computerized and Enterprise systems. Responsibilities include troubleshooting, system configuration, deployment, test protocol execution, and authoring necessary documents. Collaborate with cross-functional teams and ensure optimal system performance and user experience. Flexible position with potential for remote work.

Support cGMP QC testing for raw materials, drug substances, and finished products. Execute and troubleshoot analytical methods, support method transfers, qualification activities, and ensure compliance with cGMP standards. On-site position with 1st shift, Wed-Saturday schedule.