Regulatory Affairs Specialist Jobs in North Chicago, IL

The Director Regulatory Affairs Data Standards and Governance is responsible for driving awareness and implementation of data standards and associated best practices in systems to support Regulatory Requirements for data submissions and to enable Regulatory data to connect with data sourced from oth...

The Senior Director of Regulatory Business Excellence is accountable to lead a cross functional team of Business Process Owners as they develop implement and improve regulatory business processes across Abbvie. These business processes include improvements in how we manage existing regulatory inform...

The Senior Manager Regulatory Affairs Chemistry Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients to deliver biologics products to patients including mAb ADC and cell & gene therapies. Prepares CMC regulatory strategies that enable first pass...

The Senior Associate Regulatory Affairs Submission Management manages medium to high impact moderately complex submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams this individual establishes and maintains submission content planne...

The Senior Manager RA Global Reg Strategy US & Canada - Immunology is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. Assures that regulatory strategies defined wit...

The Senior Associate Regulatory Affairs Submission Management manages medium to high impact moderately complex submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams this individual establishes and maintains submission content planne...

The Associate Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams this individual establishes and maintains submission content planners and associated timelines...

The Device Regulatory Affairs Submission Manager is responsible for leading the planning preparation coordination and submission of regulatory dossiers for medical devices and combination products throughout the product lifecycle. This experienced professional partners with Regulatory Affairs leader...

The Director Regulatory Affairs Device is responsible for combining knowledge of scientific regulatory and business issues to support and drive strategy for regulatory submissions including new applications and amendments renewals annual reports supplements and variations. Has influence and responsi...

The Manager Regulatory Affairs Global Reg Strategy US & Canada is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. The Manager assists Regulatory Staff by identifyin...

The Associate Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. The Associate establishes and maintains submission content planners and associated timelines facilitates tactical submission team m...

The Manager Regulatory Affairs for Chemistry Manufacturing & Controls (CMC) - Biologics Product Lead works with internal and external partners in order to deliver products to patients. Prepares CMC regulatory strategies that enable first pass approvals under limited management supervision. Develops...

Oncology is a key therapeutic area for AbbVie with a portfolio consisting of both marketed products and a pipeline containing multiple promising new molecules that are being studied in nearly 200 clinical trials in 19 different types of cancer.AbbVie is focused on the discovery and development of no...

The Director of Regulatory Information Management (RIM) leads the advancement of business capabilities to enable efficient consistent and compliant use and management of Regulatory information across AbbVie and with Health Authorities. Provides strategic design implementation and ongoing improvement...

The Bel Group is a major player in the food industry through portions of dairy fruit and plant-based products and one of the world leaders in branded cheeses. Its portfolio of differentiated and internationally recognized brands includes The Laughing Cow Kiri Babybel Boursin Nurishh PomPotes and GoG...

The Manager Regulatory Affairs Device works with internal and external partners to deliver products to patients. Prepares device regulatory strategies that enable first pass approvals under limited management supervision. Develops and manages content strategy for global regulatory submissions includ...

The Director Regulatory Affairs Advanced Technology Enablement is responsible for shaping owning and executing the Regulatory Affairs (RA) AI roadmap driving strategic initiatives that embed artificial intelligence and automation within the global RA organization. This leader will serve as the key s...