1 to 15 of 36
Sort by: Date | Relevance
of Position The Scientist I is responsible for developing and characterizing novel antibody based therapies for the treatment of cancer and autoimmune disease. He/she designing biological assay systems and evaluating responses to candidate therapeutic molecules. This is a laboratory based position. Responsibilities and Job Duties Designs and implements proof of concept studies for identification o
Posted Today
of Position The responsibilities of this position include performing quality assurance activities that support all QA aspects of the analytical data, generated from the quality controls labs and raw material release, batch records review that support lot release. The incumbent in this role will review, evaluate and approve GMP data supporting various MacroGenics programs. Communicate with members
Posted 1 day ago
of Position The Supervisor, Quality Control Stability is responsible for coordinating and overseeing the stability program for MacroGenics’ products to ensure that the program is compliant with regulatory requirements and fully supports MacroGenics’ clinical and commercial programs, while also providing oversight of Quality Control Stability personnel. This individual will interact ext
Posted 2 days ago
of Position The Sr. QC Analyst – EM/Microbiology is responsible for conducting investigations, writing trend reports and working closely with the Microbiology team on environmental monitoring and utility system programs at all MacroGenics manufacturing sites to ensure compliance with cGMP standards. This position will interact extensively with other department supervisors, Quality personnel,
Posted 2 days ago
of Position The Sr IT Business Analyst is responsible for providing first level support for SAP users and subject matter experts in the materials management, production planning, manufacturing and warehouse management business areas. This role serves as a liaison between internal SAP business users and external IT/SAP vendor support. Assists in evaluating, prioritizing and managing changes to the
Posted 3 days ago
of Position The Sr. Director/Director, Facilities and Engineering is a leader responsible for oversight of all MacroGenics cGMP physical plants and non GMP sites. This individual ensures that all of our sites are operated and maintained appropriately and that our cGMP manufacturing facilities are operated and maintained in compliance with all regulations. He/she will establish both short term and
Posted 3 days ago
of Position The Sr. Clinical Research Associate will act as a key agent for the operational set up, delivery and close out of clinical trials including assisting with monitoring, day to day management of vendor interaction, and the development of study documents and plans. She/he will participate in the planning, implementation and general oversight of clinical trial activities in conjunction with
Posted 3 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 6 days ago
of Position The responsibilities of this position include performing and overseeing quality assurance activities that support all QA aspects of the drug substance release process for clinical and future commercial batches. The incumbent in this role will review, evaluate and approve all GMP data supporting various MacroGenics programs. As the lead, the incumbent will oversee the timely review and
Posted 6 days ago
of Position The responsibilities of this position include performing and overseeing quality assurance activities that support all QA aspects of the drug substance release process for clinical and future commercial batches. The incumbent in this role will review, evaluate and approve all GMP data supporting various MacroGenics programs. As the lead, the incumbent will oversee the timely review and
Posted 6 days ago
of Position The responsibilities of this position include performing quality assurance activities that support Good Manufacturing Practices (GMP) related to clinical lot release, ensuring strict compliance within MacroGenics and our external vendors . He/she will interface with other departments and will provide guidance, make recommendations and in some cases, resolve a variety of GMP and other q
Posted 6 days ago
of Position The Associate Scientist I is responsible for purifying and characterizing proteins in support of the research pipeline at MacroGenics. Responsibilities and Job Duties Purifies proteins low in endotoxin from milligram to gram scale and characterizes using SEC MALS, HPLC, and DSC to support our drug discovery pipeline Supports assay development by chemically modifying proteins with bioti
Posted 6 days ago
of Position This individual will work in a cell culture laboratory and be responsible for the expression of recombinant protein molecules in mammalian cells using various vector systems and selection methods. The candidate will be responsible for the generation and characterization of stable cell lines that express candidate clinical molecules or related proteins. Responsibilities include stable a
Posted 7 days ago
of Position The Program Manager/Sr. Program Manager is responsible for the effective management (organization, planning, execution, control and evaluation) of all aspects of pharmaceutical drug development programs. He/she will develop and manage the cross functional integrated program plan, ensuring milestones and goals are met. This individual, in concert with the Product Development Team, will
Posted 7 days ago
of Position The Calibration Technician III will complete calibrations, diagnose instrument faults, repair and perform preventive maintenance on a wide variety of equipment and instrumentation used in biopharmaceutical manufacturing and research environments, providing timely and accurate documentation of the work performed. He/she is expected to take a proactive role in supporting the Engineering/
Posted 8 days ago
Email this Job to Yourself or a Friend
Indicates required fields