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. The Senior Regulatory Affairs Specialist will be responsib...
Looking for a Regulatory Affairs Specialist with at least 2 years of regulatory experience along with submissions. Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Primary or secondary contact person for ethics committees and regulatory authorities, ...
Senior Regulatory Affairs Specialist - 2406193618WDescriptionAbiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory Affairs Specialist. The ideal candidate will:Have Regulatory Affairs experience in the medical device industry with a track record of successful FDA submis...
The Regulatory Specialist is accountable for global product compliance through design consultation, manufacturing, and post market support. STEM related Bachelor's degree or 4+ years of experience in product compliance, quality, regulatory affairs, or engineering. This role is responsible to carry o...
In this role, you will… Perform regulatory assessments for product changes including regulatory reportability decisions Work with cross functional team and international regulatory colleagues to develop and implement global regulatory strategy to support business global expansions Support regulatory...
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...
The Regulatory Operations Specialist will maintain familiarity with current regulatory submission standards and industry best practices. They will collaborate with Regulatory Affairs staff and contributing functional areas to assure adequate prioritization and scheduling of regulatory submissions. T...
GRRs purpose is to drive high quality regulatory reports through operationally efficient processes to support the production of various regulatory reports as required by Regulatory authorities. This role aligns to the Global Regulatory Reporting (GRR) Team within the CFO Global Financial Control (GF...
The Global RA Manager contributes to the Company's success by managing the Corporate R&D Pipeline (projects in R&D Development) by providing regulatory guidance to the R&D Global Core Team as well as other non-R&D functions, as needed. Accountable for global/regional regulatory strategies for new an...
Manager opportunity for Advanced Life Support (ALS) Education Programs. Adv Life Support Program - Develops, coordinate, teach and promote the Advance Life Support Programs at UNC Hospitals. This position is responsible for managing the Advanced Life Support programs at UNC Hospitals. ...
The need is for the project manager to be accountable in ensuring that assigned projects are effectively managed by taking accountability and ownership for the successful delivery of work. We are currently seeking a Technical Infrastructure Project Program Manager to join our team in Charlotte, Nort...
As an individual contributor in the Risk and Program Management Advisory Group you would be primarily responsible for supporting the creation of high-quality program materials and customer deliverables. Demonstrate technical skill according to the demands of the program, and use skill to create valu...
Analysts will work with customers to develop formalized information security policies, analyze the efficacy of current policies and procedures, and evaluate the risks posed by third-party providers. Analysts also work with the Cybersecurity Engineering team to assist clients with cybersecurity risk ...
The Director, Regulatory Affairs is responsible for assisting with establishing and managing regulatory strategies, life cycle plans, and pre/post regulatory approvals. Comprehensive knowledge of current US and ex-US regulatory guidelines, in-depth experience leading Regulatory in Global environment...
The new Global Regulatory Affairs Director is a critical hire to this organization leading PMA regulatory negotiations as the FDA point person as well as guiding clinical affairs, quality management, R&D, and all company team leaders toward successful pre-market approval. In collaboration with the V...
This job is responsible for supporting the successful implementation of the requirements of the Global Compliance - Enterprise Policy, the Operational Risk Management - Enterprise Policy (collectively "the Policies") and the Compliance and Operational Risk Management Program through partne...
Enterprise 3PD Program Management to include creation and maintenance of standard operation procedure (SOPs) documentation. ...
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 Regulatory Relations Specialist is responsible for the execution of the overall strategy for regulatory engagement and enterprise-wide standards. This includes ensuring timely response to regulatory inquiries; supporting the execution of ongoing supervision meetings; aiding with preparation of r...
At Regions, the Project Manager independently manages projects of medium to large scale that are significant in scope. This position collaborates with project teams, functional owners, and project sponsors supporting and executing the full project lifecycle to achieve specific business outcomes. Acc...
GRR's purpose is to drive high quality regulatory reports through operationally efficient processes to support the production of various regulatory reports as required by Regulatory authorities. This role aligns to the Global Regulatory Reporting (GRR) Team within the CFO Global Financial Control (G...
The Director / Associate Director of Regulatory Affairs will be responsible for contributing to the development and overseeing the implementation of global regulatory strategies for assigned programs in alignment and in compliance with local and regional requirements, and company policies. This role...
Reporting into the Chief Compliance Officer of Allspring Funds Management, LLC, the Senior Compliance Analyst will primarily support the Compliance program functions of Allspring's retail managed accounts business. The Senior Compliance Analyst will provide oversight and challenge to business compli...
The Risk and Insurance Graduate Program Manager will work collaboratively with key leaders to build, implement, and manage a pre-eminent entry program that creates a pipeline of fungible expertise across the Actuarial and IAM practices that enables recruitment of top talent while generating signific...
The Director / Associate Director of Regulatory Affairs will be responsible for contributing to the development and overseeing the implementation of global regulatory strategies for assigned programs in alignment and in compliance with local and regional requirements, and company policies. This role...