Manager, Regulatory Affairs - Durham

Summary · The Manager, Regulatory Affairs drives key regulatory activities, working seamlessly across functions to translate scientific, clinical, and technical insights into high-quality regulatory submissions while supporting regulatory strategy across the organization. This po ...

+The Director of Regulatory Affairs at Pharmaceuticals will work closely with product development core teams and sub teams in setting company goals and work closely with these groups in meeting company goals. · +Bachelor's degree required (advanced degree MS, PhD, PharmD, MD pref ...

Summary · The Manager, Regulatory Affairs drives key regulatory activities, working seamlessly across functions to translate scientific, clinical, and technical insights into high-quality regulatory submissions while supporting regulatory strategy across the organization. This po ...

Are you ready to work for a more active world? · At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our succ ...

Are you ready to work for a more active world? · At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our succ ...

Are you ready to work for a more active world? · At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our succ ...

The Director, Regulatory Affairs will lead regulatory process improvements and support regulatory activities across the United States. You will work closely with cross-functional teams, external partners, and senior leaders to simplify processes, reduce cycle times, and improve q ...

We are the makers of possible BD is one of the largest global medical technology companies in the world. · Support the monitoring and interpreting of current and new regulatory requirements and international standards for U.S. and RoW. · Lead regulatory effort to comply with new ...

+The Senior Manager of Regulatory Affairs reports directly to the Senior Director of Regulatory Affairs.This position is responsible for supporting MMS Pharmacy Automation products and associated Software and Accessories on a global basis from a Regulatory Affairs standpoint. · + ...

This position will support Regulatory Affairs projects that support the Pharmacy Automation business in BD-Connected Care. · Carry out related regulatory affairs activities such as development, execution and management of submissions. · ...

SR/DIRECTOR, REGULATORY AFFAIRS · Very late clinical stage biotechnology client focused developing innovative therapies for severe autoimmune diseases with significant unmet medical need. With a rapidly advancing and expanding pipeline, they have a need to expand Regulatory Affai ...

We are the makers of possible BD is one of the largest global medical technology companies in the world. · The Senior Manager of Regulatory Affairs reports directly to the Senior Director of Regulatory Affairs This position is responsible for supporting MMS Pharmacy Automation pr ...

Developing global regulatory submissions for medical device industry with EU MDR experience required. · ...

This position is responsible for support of a variety of regulatory activities and projects. · Assess and communicate the impact of new and changing regulatory requirements and standards. · ...

At Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advance health together. · Work arrangement - Onsite Duke Universi ...

Department: · Regulatory · Location: · Research Triangle Park, NC · Description · Kriya is a biopharmaceutical company whose mission is to develop life-changing gene therapies for diseases affecting millions of patients around the world. · We leverage our proprietary computationa ...

Regulatory Affairs Labeling - Senior Specialist/Manager · I'm currently supporting a global pharmaceutical orginzation for a newly created role within their Regulatory Affairs team. · This is a unique opportunity to play a key role in shaping global regulatory and labeling strat ...

We believe that the human element across our global teams is what allows us to continually evolve Join us and discover an environment in which you ll be supported to learn grow and become your best self Become a maker of possible with us. · Minimum of 8 years of directly related ...

Description · Kriya is a biopharmaceutical company whose mission is to develop life-changing gene therapies for diseases affecting millions of patients around the world. · We leverage our proprietary computational engine, in-house manufacturing infrastructure, and integrated de ...

We are seeking a Regulatory Affairs Specialist to support regulatory submissions lifecycle management and compliance activities for pharmaceutical or medical device products. · 2–5+ years of Regulatory Affairs experience (Pharma Biotech or Medical Devices) · Strong knowledge of F ...