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The Lead, Human Factors Engineering will be serve as a local leader for the Human Factors Engineering Team as it grows. This role will lead human factors work to support the development of devices and combination products for delivery of our wide portfolio of drugs and biologics. This includes leadership in human factors planning, use-related risk management, requirements development and execution of human factors research (user research, formative and summative studies).1. Responsible for....


The Supplier Relationship Manager manages supplier relationships. - Lead and be accountable to CDA, NDA, MSA, Quality agreement, and supplier agreements - Follow business processes and guidelines to act as the center of excellence for legal and financial aspects of the alliance - Contribute to negotiation of contract terms and conditions, including the management of amendment activities. - Contribute to tactical and strategic sourcing activity - Prepare and facilitate quarterly business review

- Madison, WI

Director - QC Stability & Release Testing (GMP), your basic purpose will be to ensure efficient and effective management. You will supervise and assist group leaders and scientists in laboratory operations with tasks such as scheduling, resource management, technical and compliance related issues. In addition, you will plan, direct and implement improvements in systems, processes and procedures to increase efficiency, productivity and quality in the laboratory. You will assist the division


Director Analytical Method Development & Validation (GMP Biopharmaceutical - PhD preferred or MS with LOTS (5+ mgt, 10+ GMP) - Analytical Method Dev’t, qualification and validation experience required - Complex and New Method work - Large Cell experience is a must - Would love to have protein Characterization and analytics - GMP and STRONG leadership (team up to 60-100), Financial Management


The Head of Device SRM (Supplier Relationship Management) manages device supplier relationships. This is a strategic role that will develop and implement internal policies and be influential in decision making across major functional areas: - Develop and manage Suppliers for clinical and commercial devices - Development and implementation for legal and financial aspects of the alliance - Contribute to negotiation of contract terms and conditions, including the management of amendment....

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