- City of New York (New York, NY)
- …Program Supervisor, the Customer Information Representative I will serve as Permit Specialist and will work within DEP's Access Permit Office (APO) to facilitate ... Training, advising and aiding staff in using information technology systems to obtain information to respond to issues, maintain...equivalent. To be eligible for assignment to Assignment Level II , candidates must have, in addition to meeting the… more
- Abbott (Pleasanton, CA)
- …**Preferred Qualifications** + Minimum of 5 years' experience working with Class II and/or Class III medical devices. Regulatory Affairs Certification (RAC) ... Opportunity** We are recruiting for a **Senior Regulatory Affairs Specialist ** to join our team on-site in Pleasanton, CA....are entered into the regulatory submission database and file systems . Ensures that details of any new or modified… more
- Abbott (Plymouth, MN)
- …from medical device, pharmaceutical, or healthcare industry + Advanced level degree + Class II or Class III medical device experience + Experience with PMA ... **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist ** to join our team on-site in Plymouth, MN. In this role,… more
- Guidehouse (Charleston, SC)
- …compliance with Authority to Operate (ATO) requirements or CSSP Accreditation. The specialist shall be capable of evaluating security solutions to ensure they meet ... + Penetration Test/Red Teaming. + Hold Information Assurance Technical (IAT) II certification. + Hold at least one of the following Certifications:… more
- Fluor (Aiken, SC)
- …provide proof of US citizenship * E/P/C experience: Engineering and/or Construction (Project Engineer II or III ) * Has had a broad exposure to Engineering, ... as 4 years * Has fulfilled role of CM specialist driving (the 5 key elements of) CM across...project execution success. * Good, solid knowledge of typical software/ systems tools used in our industry. * Known to… more
- Serco (Fort Bliss, TX)
- …configuration documentation, routing tables, and interconnect diagrams in support of Level I, II , and III Technical Data Package (TDP) deliveries. + Maintain the ... has a great opportunity for you! The Configuration Management Specialist will be part of a dynamic team at...and other Serco functional area teams to deliver quality systems and associated supporting documentation. The team has been… more
- Globus Medical, Inc. (Audubon, PA)
- …approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA ... lives as quickly as possible. **Position Summary:** The Regulatory Affairs Specialist assists with drafting, submitting and gaining clearance for 510(k) submissions,… more
- Queen's Health System (Honolulu, HI)
- …with special projects as assigned. * Performs duties of a Professional Billing Specialist as needed. II . TYPICAL PHYSICAL DEMANDS: * Essential: sitting, ... on denied claims in accordance with policies and procedures of The Queen's Health Systems (QHS) and The Queen's Medical Center (QMC) and in compliance with federal,… more
- Abbott (Alameda, CA)
- …Directive (98/79/EC). Preferred Qualifications . 5 years' experience working with Class II , Class III medical devices and/or biologics/drugs. Regulatory Affairs ... glucose levels with our new sensing technology. The Opportunity The Principal RA Specialist -Business Partnerships will work on-site out of our Alameda, CA location… more
- MUFG (Tempe, AZ)
- …and monitoring tools for tracking performance metrics and process efficiency. **TPRM Specialist ** + Ensures that all Third-Party Risk Management (TPRM) Policies & ... Responsible for quality of documentation in FLoD and TPRM systems . + Responsible for information sharing about the Third...laws (including (i) the San Francisco Fair Chance Ordinance, ( ii ) the City of Los Angeles' Fair Chance Initiative… more