Looking for a Regulatory Affairs Specialist with at least 2 years of regulatory experience along with submissions. Primary or secondary contact person for ethics committees and regulatory authorities, project teams on all regulatory-related issues, and co-contractors, subcontractors, and third- part...
The Senior Manager/Director of Policy and Regulatory Affairs will play a pivotal role in shaping and advancing our client's strategic initiatives across PJM and regulatory landscapes. Director of Policy & Regulatory Affairs | Eastern US, REMOTE |$165k - $175k base + bonus. Are you a regulatory affai...
Senior Regulatory Affairs Specialist. A leading global medical device company is looking for a motivated and experienced individual to join their team as a Senior Regulatory Affairs Specialist at their facility in the greater Charlotte area. This role involves ensuring regulatory compliance and navi...
Job Description SummaryThe New Plant/Product (NPP) Licensing Manager will establish the vision & strategy and drive execution for Regulatory Affairs to accelerate the licensing needed to deploy new technologies. The role is in Regulatory Affairs and reports to the General Manager of Nuclear Programs...
Senior Regulatory Affairs Specialist. Summary:A leading global medical device company is looking for a motivated and experienced individual to join their team as a Senior Regulatory Affairs Specialist at their facility in the greater Charlotte area. This role involves ensuring regulatory compliance ...
At Thermo Fisher Scientific, the Regulatory Affairs function plays a vital role in ensuring compliance with the ever-evolving global regulations governing our industries. They collaborate closely with cross-functional teams, such as Research and Development, Quality Assurance, and Manufacturing, to ...
The AD, Regulatory Affairs is responsible for coordinating the regulatory activities for projects including new products and life cycle management. Provides guidance to product core teams to ensure that all regulatory submissions are planned, communicated, and executed per regulatory and business re...
The Senior Manager, Regulatory Affairs is an experienced leadership position with a deep understanding of global regulatory requirements, a strong track record in navigating complex regulatory landscapes, and the ability to collaborate across cross-functional teams. The Senior Manager of Regulatory ...
Accountable for global/regional regulatory strategies for new and existing products in collaboration with the Global Regulatory Team (GRT). Manages and leads the preparation and review of regulatory applications, reports, and correspondence in a manner that ensures timeliness, accuracy, comprehensiv...
The Regulatory Affairs Senior Specialist - Medical Devices coordinates the regulatory activities for development projects including new products and life cycle management. This includes assisting with regulatory strategies and timelines as well as the development and implementation of submissions un...
This goal must be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process and policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. The Associate Director will b...
The Opportunity: Verona Pharma is currently recruiting a Senior Director, Regulatory Affairs to join our team, reporting to our Senior Vice President, Regulatory Affairs. In the role of Senior Director, Regulatory Affairs, you will be responsible for overseeing and directing regulatory activities fo...
This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. Accountable to GRL (if one as...
Pharma and Personal Care – Regulatory Affairs Manager/ NA Regulatory Business Partner . Collaborate with global PPC and NA regulatory partners and Marketing & GTC teams to develop and execute regulatory intelligence programs that converts regulatory change information to actionable insights. Drive r...
This goal must be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process and policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. Accountable to GRL and Global...
STEM related Bachelor's degree or 4+ years of experience in product compliance, quality, regulatory affairs, or engineering. The Regulatory Specialist is accountable for global product compliance through design consultation, manufacturing, and post market support. This role is responsible to carry o...
Implement worldwide regulatory registration strategy, Communicate and negotiate with local market authorization holders/ distributors / regulatory authorities information required and prepares regulatory submissions to be used worldwide for all marketed products. Coordinate and interact with domesti...
Director, Regulatory Affairs . Present regulatory data needs, negotiate with and influences management, colleagues and partners to ensure regulatory data requirements are met. Serve as the Regulatory Affairs representative on cross-functional teams. Serve as the OPI Regulatory Affairs representative...
You will work with cross functional groups and coordinate and collaborate with business and support teammates to provide support on regulatory responses alongside compliance, risk, strategy, and operations partners including Regulatory Relations, Regulatory Strategy, and Regulatory Affairs. Responsi...
Associate Director, US Regulatory Affairs, Advertising & Promotion - Permanent - Raleigh, NCProclinical is seeking an Associate Director, US Regulatory Affairs, Advertising & Promotion for a large global pharmaceutical company with locations in New Jersey, North Carolina and Massachusetts. The Assoc...
Regulatory Affairs Strategy and Management:. Manage and lead the preparation and review of US regulatory applications, reports, and correspondence in a manner that ensures timeliness, accuracy, comprehensiveness, and compliance with internal and external regulatory standards. Regulatory Affairs Info...
They will collaborate with Regulatory Affairs staff and contributing functional areas to assure adequate prioritization and scheduling of regulatory submissions. The Regulatory Operations Specialist will maintain familiarity with current regulatory submission standards and industry best practices. P...
Connections working at Duke University Health System https://regulatorycareers. ...
When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above.The information that you have provided in your cover letter and CV will be used to assess your applicatio...
Quality/Risk Management Worldwide Regulatory Affairs. Regulatory Science from UNC, you will be prepared to play a critical role in the public or private sector to ensure that pharmaceutical products are safe and effective for human use. You'll acquire the professional savvy that this field demands a...