1 to 15 of 29
Sort by: Date | Relevance
of Position The Manufacturing Associate I 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 requirements.
Posted 11 days ago
of Position The Clinical Quality Assurance (QA) Manager is responsible for managing the execution of the Company's audit plans and strategies through the auditing of investigator sites, vendors and internal systems to ensure overall quality system compliance for Clinical. Key Responsibilities Manages and/or conducts the planning, execution and resolution of investigator si
Posted 11 days ago
of Position The Development Scientist I/II is responsible for the development of Drug Product (DP) formulation and manufacturing processes for the Company's pipeline molecules across early and late stage clinical and commercial development. Represents the Drug Product Sciences (DPS) group in cross functional project teams and leads DP development activities within DPS, inc
Posted 11 days ago
of Position The Development Scientist I/II is responsible for the development of Drug Product (DP) formulation and manufacturing processes for the Company's pipeline molecules across early and late stage clinical and commercial development. Represents the Drug Product Sciences (DPS) group in cross functional project teams and leads DP development activities within DPS, inc
Posted 12 days ago
of Position The Manufacturing Associate II/III 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 requireme
Posted 12 days ago
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 data sets. Prepares reports of clinical trial studies for internal validat
Posted 12 days ago
of Position The Scientist II position is a technical managerial position responsible for development, qualification, method transfer and full lifecycle support of analytical release methods for biologic products using a variety of scientific processes and methodology. This individual will work closely with other development and quality functions in a results driven, collab
Posted 12 days ago
of Position The Vice President/Executive Director, Drug Product Safety (DPS) is responsible for establishing a global strategy for drug safety and for influencing the drug safety mindset in support of our company mission and long term objectives. He/she will lead the team, focused on leading and scaling a Drug Safety/Risk Management/Pharmacovigilance program for pre and po
Posted 12 days ago
of Position The Sr. Manufacturing Outsourcing Manager is accountable for effective supply chain management of cell banks, drug substance and drug product sourced from external Contract Manufacturing Organizations (CMOs). He/she is responsible for contract and alliance management with external manufacturing partners to ensure product supply for MacroGenics' portfolio. The M
Posted 12 days ago
of Position The Sr. Director/Director, Analytical Sciences is responsible for leading a diverse department in the development, qualification and transfer of methods that demonstrate the safety, purity and potency of molecules across the entire portfolio and through all stages of clinical development via release, characterization and stability testing. In addition, he/she w
Posted 12 days ago
of Position The Sr. Business Relationship Manager/Business Relationship Manager R&D IT will establish stronger capabilities in support of technology evaluation, IT delivery, and IT business relationship management within the newly formed IT department. He/she will act as an IT Program Delivery and Business Relationship Manager and will support the Research, Clinical, and D
Posted 12 days ago
of Position The Sr. Regulatory Operations Manager/Regulatory Operations Manager position is responsible for assisting the Director, Regulatory Operations in enforcing MacroGenics regulatory submission standards and current electronic submission guidelines/requirements. The incumbent in this role will be responsible to managing day to day submission related tasks and may be
Posted 12 days ago
of Position The Vice President of Regulatory Affairs will be responsible for developing the global regulatory strategy for development stage programs including CMC, regulatory submissions, regulatory compliance, regulatory advice and counseling, advertising and promotion review, and product registrations across the product portfolio as well as lifecycle of all products, as
Posted 12 days ago
of Position The Sr. Automation Engineer/Automation Engineer III is responsible for executing automation tasks related to design, implementation and management of Process Control Systems, Building Automation Systems, Data Historians and associated control system integration. The position will develop automation requirements and be responsible for the design, budgeting, sche
Posted 12 days ago
of Position The FP&A Manager will play a key role in assisting with the planning, organizing and the successful execution of all aspects of the annual budget and quarterly forecast of the consolidated three year operating plan. Incumbent partners proactively with department heads to deliver actionable, meaningful, accurate and timely reporting, analysis, insights and plans
Posted 12 days ago
Email this Job to Yourself or a Friend
Indicates required fields