Regulatory Associate - Cary, NC

+The Regulatory Associate is responsible for drafting, managing and maintaining the pre-production label portfolio of pesticide products. The role involves ensuring that labels comply with government regulations, are current and competitive, and collaborating with internal teams ...

The Regulatory Associate is responsible for drafting, managing and maintaining the Atticus pre-production label portfolio. · Atticus is serious about the success of this industry as well as the success of our team. We're on a number of important task forces that support the indus ...

The Regulatory Associate is responsible for drafting, managing, and maintaining the Atticus pre-production label portfolio. Ensure that pesticide labels comply with government regulations. Collaborate with internal Commercial teams to ensure commercial elements on labels (Graphic ...

The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care contribute to the development of society by anticipating the changing needs of those around the world. · We look for candidates that offer a fresh per ...

The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those around the world. · ...

The Associate Director, Regulatory Operations & Projects is responsible for managing Liquidia's regulatory operations and regulatory infrastructure projects in the planning, coordination, · & execution of global regulatory submissions, document management activities, · & evolving ...

+The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical devices and IVD products. · +The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for me ...

The Associate Director is responsible for preparing and managing regulatory CMC submissions to support clinical development registration and lifecycle management for assigned project including small molecules inhaled therapies and drug-device combinations. · Contributes to the gl ...

The Associate Director Regulatory Affairs – CMC is responsible for preparing regulatory submissions to support clinical development registration lifecycle management assigned project including small molecules drug-device combinations. · ...

The Associate Director, Regulatory CMC Small Molecule Lead will play a pivotal role in shaping and executing the global Regulatory Chemistry, Manufacturing and Controls (RegCMC) strategy for Biogen's small molecule portfolio. · ...

The Associate Director/Director, Regulatory CMC reports to the Vice President of Regulatory CMC and is responsible for managing the Company's Regulatory CMC function to enable clinical development, marketing authorization, manufacture, and distribution of clinical supplies and co ...

As the Associate Director, Regulatory Affairs-Advertising and Promotion you will be tasked with the important role of leading the company's regulatory oversight of promotional activities for its expanding healthcare product portfolio. · ...

+We are looking for candidates from the regulatory PRC side, often referred to as being part of the MLR regulatory team. The Associate Director, Regulatory Affairs will lead the company's regulatory oversight of promotional activities for its expanding healthcare product portfoli ...

The Associate Director Regulatory Affairs is responsible for leading and managing the Company's regulatory oversight of promotional activities for its expanding healthcare product portfolio. · ...

As Associate Director Regulatory CMC Small Molecule Lead you will play a pivotal role in shaping and executing the global Regulatory Chemistry Manufacturing and Controls RegCMC strategy for Biogens small molecule portfolio. · ...

The primary purpose of the Global Solutions team is to support our broker clients in the global marketplace through notification of shareholders of general meetings. · Interpret and apply global regulatory requirements to all daily tasks. · Create and validate global corporate ac ...

We are seeking a Crop Protection Regulatory Manager to lead the timely acquisition and maintenance of federal pesticide registrations for UPL. The ideal candidate will possess a minimum of bachelor's degree within Agriculture or related scientific discipline with at least 5+ year ...

+ The State Regulatory Manager is responsible for obtaining the state registrations and maintaining marketability of assigned product lines.The job requires a minimum of a bachelor's degree with approximately 5 or more years' direct hands-on industry experience in the US State Re ...

The Executive Director serves as the chief staff executive responsible for leading the operations performance and strategic execution of INDA the Association of the Nonwoven Fabrics Industry a founding member of the Global Nonwovens Alliance GNAStrategic Leadership Develop and ex ...

VQ Biomedical is an early-stage medical device company developing the first ever minimally invasive catheter designed to deliver oxygen directly into the bloodstream. · The Director of Quality & Regulatory will lead all aspects of the quality management system. · ...