of Position The Vice President, BioPharmaceutical Development is a strategic leader responsible for oversight of Cell Line Development, Cell Culture Sciences, Purification Sciences, Analytical Sciences and Drug Product Sciences. This individual will drive early and late stage development and optimization of our antibody, antibody drug conjugates, and multi specific protein

of Position The Sr. Facilities Planner Scheduler/Facilities Planner Scheduler III is responsible for supporting the coordination of facility maintenance activities of all buildings, utilities, and equipment in a GMP regulated facility. This individual maintains documentation of all activities through the Blue Mountain Regulatory Asset Manager system to ensure compliance wi

of Position The Associate Scientist I/II will be part of a translational biomarker unit, part of the Cell Biology and Immunology group, focused on characterizing novel antibody based therapies for the treatment of cancer. In this position the employee will be responsible for evaluating biological responses to candidate therapeutic molecules in a range of phenotypic analyse

of Position The Manufacturing Associate I/II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics' multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirement

of Position The Manufacturing Associate I/II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics' multiple clinical programs in the Protein Purification area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory req

of Position The Research Associate II / Associate Scientist I position will support preclinical development of MacroGenics antibody drug conjugates (ADC) through cell line engineering and molecular biology support. This position will independently develop and engineer cell lines, and conduct cell based, molecular, and biochemical assays which contribute to the ADC research

of Position The Sr. Director/Director, Clinical Operations is responsible for providing strategic vision and direction within the department of Clinical Operations. Ensures completeness and consistency of processes required for successful life cycle management for all phases of clinical trials across the therapeutic portfolio. Responsibilities and Job Duties Provides input

of Position The Intern will be working in the Antibody Engineering Department of MacroGenics, implementing techniques in protein production and purification to produce membrane proteins encapsulated in nanodiscs, synthetic model membrane systems, for use in antibody discovery and in vitro assays. The intern will be responsible for establishing protocols for nanodisc genera

of Position This role reports to the VP Targeted Therapeutics. This individual will be a key member of the team responsible for progressing the Company's antibody based oncology product candidates through pre clinical and early clinical development, achieving key program milestones and timeline goals. Key Responsibilities Leads and supports advancement of molecules from le

of Position The Senior Clinical Supplies Manager is a key member of the clinical development team and assists in the oversight of all aspects of clinical supply planning, forecasting, capacity planning, labeling/packaging, distribution and risk management for all MacroGenics' clinical products/clinical trials. He/she works closely with Director, Clinical Pharmacy, Clinical

of Position The Clinical Supplies Manager assists in the oversight of all aspects of clinical supply planning, forecasting, capacity planning, labeling/packaging, distribution and risk management for all MacroGenics' clinical products/clinical trials. He/she works closely with Director, Clinical Supplies, Clinical Operations, Clinical Research, CMC, Regulatory Affairs CMC,

of Position The SharePoint Developer will help us improve our current Quality department SharePoint site. We're looking for someone who is experienced in SharePoint development and can help us create a more efficient and user friendly site. Responsibilities and Job Duties Translate user requirements and functionality into technical design specifications and workflows. Deve

of Position The intern will be developing a new, highly efficient molecular technique to create mutations in plasmids for the purpose of antibody engineering. Current methods to construct large synthetic antibody libraries are hindered by low transformation efficiency (PCR digestion ligation method), low recombination rate (Kunkel method) or a multi step process with limit

of Position The Clinical Operations Intern will work on trials that are expected to be in various stages of start up and participate as an active member of an ongoing Clinical Study team. The Director of Clinical Operations, will act as the mentor and hiring manager for this summer intern position. Consulting and training will also be provided by other Directors in Clinica

of Position The intern will be responsible for assisting and supporting the characterization studies of company's pipeline molecules. Responsibilities and Job Duties Assisting and support the characterization studies of company's pipeline molecules under supervision. Making buffers and reagents according to the written SOPs Assisting experimental design, execution, sample,