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 Research Associate II/Associate Scientist I will be part of the Targeted Therapeutics Group focused on generating novel antibody based therapies for the treatment of cancer and autoimmune diseases. The encumbent will be responsible for designing and executing experiments to produce and characterize novel antibody drug conjugates (ADCs) to treat a variety of

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 Data Manager II collaborates with various departments on the design, documentation, testing and implementation of clinical data studies. Develops systems for organizing data to analyze, identify and report trends. Analyzes the interrelationships of data and defines logical aspects of datasets. Prepares reports of clinical trial studies for internal validati

of Position The Manager, Metrology is responsible for defining, leading, and managing the calibration function at MacroGenics. These responsibilities include running the day to day operations of the calibration department, managing long term expectations of the group, serving as system owner of the computerized maintenance database system, and overseeing the administrative

of Position This position is responsible for representing the Quality Assurance (QA) Operations department providing strategic development, quality leadership, project management and technical knowledge/key support to all aspects of a project. Individual will be fully competent in Quality Assurance systems and understanding how they interlink with other business systems. I

of Position This position is responsible for performing activities to support analytical testing programs at MacroGenics to ensure compliance with cGMP standards including in process, product release and stability testing. This individual will guide and partner with lower level QC analysts to provide feedback and technical information. This individual will also ensure accu

of Position The Associate Program Management Director/Program Management Director will drive the program teams forward in the development of novel antibody based therapeutics within our oncology portfolio. They will work in close coordination with scientific team leads and cross functional Program Development Teams (PDTs) to enable the execution of the program strategy. Th

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 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 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