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...
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 ...
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...
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 ...
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...
Assist in various regulatory duties including completion of deliverables and preparation of regulatory submissions for the next-gen clip system. Minimum of years of experience in regulatory affairs. Provide regulatory support for manufacturing-related submissions and international submissions and re...
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. ...
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...
The Incubator Program Manager (IPM) will manage all aspects of the incubator program including monitoring leased space occupancy, ensuring adherence to safety procedures, onboarding new tenants, ensuring lease agreements are current, and that lease payments are collected. This position has primary r...
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...
The program will focus on producing local ecotype seeds for regions throughout Georgia where there is significant demand from numerous fully funded ongoing habitat conservation and restoration projects. The successful candidate's primary role will be to serve as the Program Manager of the Georgia Na...
THE ARMY HEALTH CARE ADVANTAGE.As a member of the Army health care team, you’ll receive benefits that you won’t be able to get in a civilian career.Feel inspired with great case diversity and over 40,000 visits coming into the U.Army medical facilities and clinics around the world every day.See and ...
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 ...
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. ...
Bachelor's degree in a relevant technical field (Engineering, Technical Communication, etc. Proven experience as a technical writer in a manufacturing or engineering environment. Develop clear, concise, and accurate technical documentation, including user manuals, standard operating procedures (SOPs...
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...
Senior Project Manager with extensive experience in HVAC, pipefitting, and sheet metal installations. This role requires a combination of technical expertise, strategic project management, and leadership skills to oversee projects from planning through to successful execution and completion. Develop...