Job description As the Head of Regulatory Reporting Transaction Testing, you will be responsible for building a new regional and/or global transaction testing function to help ensure the integrity of regulatory reporting data and processes. The new team will primarily test balances and transactions included in key regulatory reports and validate whether those transactions

Develop, lead, and execute the company's regulatory compliance strategy including Drugs and Medical devices. Ensure complete compliance with all FDA, QSR, cGMP, and other federal and state regulations, and with corresponding international regulations in all markets served. The scope of this position impacts all products in all phases of manufacturing and service. Job Duti

Confer with VP of Quality and Regulatory to establish and prepare appropriate worldwide regulatory strategies and filings for product approvals Oversee the development and implementation of global regulatory strategies including US, Europe, UK, Canada, Asia, Australia Review changes in international laws and regulations and assess their impact and make recommendations to

At Horizon Therapeutics, we define success by the number of lives touched, lives changed, and lives saved. Our global biotechnology company is made up of agile, out of the box thinkers with a focus on delivering breakthrough medicines to those living with rare, autoimmune, and severe inflammatory diseases. This is the heart of our global mission. Start a career that enable

Leads regulatory activities for medical device, over the counter, and prescription drug products. Essential Duties and Responsibilities Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Compiles and prepares regulatory documents (summary technical documents, essential requirements checklists, 510(k)'s, EU des

Develop and maintain procedures to ensure regulatory compliance with government regulations. Respond to requests from governmental bodies. Review notifications of activity when they occur. Receive copies of governmental reports from such activities and ensure facility retains appropriate documentation relative to the inspections, and timely completion of any corrective ac

The Regulatory Affairs Manager is responsible and accountable for Company Core Data Sheets (CCDS), Company Core Safety Information (CCSI) and Reference Safety Information (RSI for assigned products, including regulatory responsibilities in associated change control and labeling processes. This person is instrumental in the design, development, and maintenance of global re

Duties WHAT IS THE AP APPEALS DIVISION? A description of the business units can be found at Vacancies will be filled in the following specialty areas Office of Appeals Specialized Examination Programs and Referral Technical Guidance Conducts Appeals conferences for the settlement of the largest and most complex tax cases in which taxpayers have appealed determinations mad

JOB ANNOUNCEMENT PROJECT COORDINATOR Department of Administrative Hearings Number of Positions 1 Description Under the direction of the Deputy Director of Administrative Adjudication, serves as a direct liaison with Corporation Counsel's Office regarding filing deadlines in Administrative Review (Appeals) matters pending in the Circuit Court of Cook County. Coordinate wit

JOB ANNOUNCEMENT Supervisor of Personnel Administration, BX17 Chicago Department of Aviation Human Resources Division Number of Positions 1 Starting Salary $78, 276.00 ESSENTIAL DUTIES Oversee and management the CDA's annual Winter Snow Season PTMD hiring process . Supervises staff engaged in coordinating the interviewing and hiring of employees. Directs staff engaged in

JOB ANNOUNCEMENT PROJECT COORDINATOR (Affordable Requirements Ordinance) DEPARTMENT OF HOUSING Policy Division Number of Positions 1 Starting Salary $65,688.00 Under supervision of the Affordable Requirements Ordinance (ARO) Project Manager, position serves as the team lead for the ARO, which coordinates the production of affordable housing units and other contributions g

Manage Labeling and Ad/Promo reviews including communication and education of regulatory requirements for FDA, ISO, CMDR, IEC, and Prop 65. Conduct 510k decision checklists, LTF, and 510k submission reviews. Prepare, or direct consultants in preparation of, required regulatory filings, including 510k for FDA clearance. Work with Omron Healthcare Headquarters to ensure req

Manage Labeling and Ad/Promo reviews including communication and education of regulatory requirements for FDA, ISO, CMDR, IEC, and Prop 65. Conduct 510k decision checklists, LTF, and 510k submission reviews. Prepare, or direct consultants in preparation of, required regulatory filings, including 510k for FDA clearance. Work with Omron Healthcare Headquarters to ensure req

Duties WHAT IS THE APPEALS Division? A description of the business units can be found at Vacancies will be filled in the following specialty areas Office of Appeals Collection Appeals The following are the duties of this position at the full working level. If this vacancy includes more than one grade and you are selected at a lower grade level, you will have the opportuni

To follow the OCFO (Own Control Flight Operations) lead on offering prime service to those moving airfreight within the OCF Network. Maximum utilization of capacity suiting the service and cost requirements of the shipments tendered, by mixing and configuring cargo as instructed. We offer We offer you an exciting global career at the forefront of world trade. Working with