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of Position The Manufacturing Associate I 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 requirements. Responsibilities
Posted 1 day ago
of Position The Automation Engineer II/III plays an active role in executing automation tasks related to design and implementation of a Process Control System, Building Automation System and system integration. The position will define scope, develop automation requirements and be responsible for design, specifications, budgeting, scheduling, resource management, implementation, and commissioning.
Posted 4 days ago
of Position As a member of the Information Technology team, the Network Analyst III will be responsible for efficient and reliable operation of the MGNX infrastructure. This individual will be passionate about customer service. You will work in a team setting and take a lead role in the team to ensure the work is completed. This position requires the ability to handle tactical matters such as serv
Posted 8 days ago
of Position The Scientist II is a key team member focused on early and late stage process development and optimization, as well as late stage process characterization and validation of cell culture processes. This individual will be responsible for managing and leading cell culture projects and for solving scientific problems related to robust process development and characterization. This individ
Posted 9 days ago
of Position This is a non supervisory, entry level position responsible for executing key document control related activities that support the various departments operating under GxPs. This position requires frequent interaction and communication with the various GxP departments to ensure that document related requirements are supported and timelines are met. Responsibilities and Job Duties Routin
Posted 16 days ago
of Position This position is responsible for performing activities in support of the microbiology and environmental monitoring testing programs including monitoring of the manufacturing cleanrooms. This individual will be required to complete the testing and related documentation in a timely manner while adhering to standard operating procedures and under cGMPs . Responsibilities and Job Duties Co
Posted 22 days ago
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 be required to complete the testing and related documentation in a timely manner while adhering to standard operating procedures and under cGMPs. Responsibi
Posted 22 days ago
of Position The Supervisor, Quality Control Raw Materials is responsible for managing, monitoring and reporting Quality Control raw material schedules and results to ensure the department fully supports MacroGenics' cGMP validation, clinical and commercial activities, and programs, while also providing oversight of Quality Control raw materials personnel. This individual will interact extensively
Posted 22 days ago
MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody based technologies. Our team of 300+ dedicated individuals is advancing a pipeline of product candidates to treat patients with cancer as well as various autoimmune disorders and infectious diseases. Our products and platforms have attracted multiple partnerships with leading
Posted 24 days ago
None Preferred Qualifications Certification as Quality Auditor Experience with electronic learning and quality management systems Experience with SAP system MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, disability, protected vetera
Posted 24 days ago
Associate Director, Clinical Operations Clinical Project Manager Clinical Research Associate Preferred Qualifications Master's Degree in health care, life sciences, or related discipline MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age
Posted 24 days ago
Manages the team to ensure that priorities for lab scheduling, logistics and flow of activities for testing and review are established and followed and that workload is also prioritized, and staffing is maximized to ensure timely and effective performance. Provides direct supervision of QC analysts performing routine GMP testing of potency, bioassay, ELISA and related methods, assuming primary res
Posted 24 days ago
No Preferred Qualifications Master's Degree in a scientific discipline, Mathematics, or Computer Science. Some experience with oncology clinical trials and CDISC data models Statement MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, d
Posted 24 days ago
No Statement MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, disability, protected veteran status, or any other characteristic protected by federal, state or local law. We are committed to working with and providing reasonable accomm
Posted 24 days ago
of Position The Senior Principal SAS Programmer provides timely lead programming to clinical study teams on all programming matters, including the most complex, and provides programming and technical leadership to the Clinical Programming group. Assumes the role of a lead programmer on studies. Create, document, and validate corresponding related SAS systems, programs, datasets, and outputs needed
Posted 26 days ago
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