Defining worldwide regulatory requirements necessary for regulatory approval of products. Minimum 5-8 years' experience in Regulatory Affairs in the medical device industry. Preparing documentation for international regulatory registrations. Participating in cross functional teams as regulatory lead...
Our client is seeking a highly skilled and motivated Senior Specialist in US Regulatory Affairs Operations. This is a fantastic opportunity for a seasoned regulatory affairs professional to make a significant impact in a fast-paced environment. Joseph, MO or Athens, GA, offers a unique opportunity t...
Job Title: Senior Specialist, US Regulatory Affairs Operations. Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakehol...
Sr Regulatory Affairs Specialist. Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakeholder groups relative to regulat...
Job Title: Senior Specialist, US Regulatory Affairs Operations. Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakehol...
Title: Regulatory Affairs Specialist I. Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakeholder groups relative to r...
Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of BIAH products an...
Title: Regulatory Affairs Specialist I. Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakeholder groups relative to r...
Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of BIAH products an...
Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of BIAH products an...
Sr Regulatory Affairs Specialist. Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within the regulatory department and stakeholder groups relative to regulat...
Defining worldwide regulatory requirements necessary for regulatory approval of products. Minimum - years' experience in Regulatory Affairs in the medical device industry. Preparing documentation for international regulatory registrations. Participating in cross functional teams as regulatory lead. ...
Ability to support Program Manager in cost, schedule, and performance of program. Ten (10) years' experience as a program or project manager in managing programs and contracts of similar scope, type, and complexity is required. Deputy Program Manager, SIGINT, Airborne ISR. We're searching for a tale...
This position has primary responsibility for managing the incubator program and makerspace within Innovation Gateway, UGA's commercialization program in the Office of Research, which encompasses the University's intellectual property licensing and startup support functions to ensure that research di...
Novex is seeking a Program Manager to lead a program within our Next-Gen portfolio!. Fifteen (15) years experience as a program or project manager in managing programs and contracts of similar scope, type, and complexity is required. Serves as the main point of contact for the Contracting Officer (C...
During the initiation phase of the project, the Site Project Manager will work alongside the Meditech Project Manager to complete foundational items for the project and subsequently communicate them to the organization’s stakeholders. The Client Site Project Manager will serve as the hospital ...
The Construction Project Manager candidate must be well-versed in all construction methodologies and procedures and able to coordinate a team of professionals of different disciplines to achieve the best results. Responsible for coordinating and scheduling work on multiple projects and will interact...
We’re looking for a Regulatory Affairs Specialist to manage data maintenance and regulatory submissions. Contract Job Opportunity: Regulatory Affairs Specialist. Handling data management and retrieval of regulatory documents. Preparing and submitting US regulatory filings on time and in compliance. ...
Ensures compliance of MARTA’s Drug & Alcohol Program (Drug and Alcohol Policy and Department of Transportation (DOT)/FTA regulations 49 Parts 40 and 655) in collaboration with the business unit's OMS Specialist. Conducts safety-sensitive contractor Drug & Alcohol oversight, including review and iden...
Project Manager to join their team. Are you floored by the idea of managing commercial flooring projects? Well, buckle up because we have an amazing opportunity for you!. In this role, you will be responsible for overseeing commercial flooring projects from start to finish. From coordinating with su...
Assist in various regulatory duties including completion of deliverables and preparation of regulatory submissions for the next-gen clip system. Minimum of 7 years of experience in regulatory affairs. Provide regulatory support for manufacturing-related submissions and international submissions and ...
Trade Compliance Analyst to join our team in Duluth, GA. In this role you will apply your expertise of interpreting and applying Trade Compliance rules and regulations while supporting trade compliance, import and export daily activities and operational goals. Responsible for Trade Compliance for Im...
Assist in various regulatory duties including completion of deliverables and preparation of regulatory submissions for the next-gen clip system. Minimum of 7 years of experience in regulatory affairs. Provide regulatory support for manufacturing-related submissions and international submissions and ...
Contributes to maintaining the Ethics and Compliance risk assessments at the compliance risk, product, business process, or overall enterprise level. Responsible for supporting Ethics and Compliance CMS Analytics and Reporting. Serves as a liaison between Compliance, Information Technology, Line of ...
Demonstrated successful leadership experience, including in multi-functional teams including Global Sales & Marketing (GSM), Regulatory, Legal, Clinical/Medical Affairs, Quality, Corporate Communications, and other Functional Departments. Advanced experience with regulatory review of labeling · Expe...