regulatory Jobs in Chicago, IL

Refine Results
1 - 6 of 6 Jobs

IT Business Relationship Manager - Quality, Regulatory and R&D

Abbott Laboratories

Lake Forest, Illinois, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future

Regulatory Consultant

Randstad Digital

Remote or Portland, Maine, USA

Contract

job summary: SUMMARY OF DAY-TO-DAY RESPONSIBILITIES: Provide support and delivery of requirements and work packages on low complexity projects/initiatives in alignment with business strategies. May also support team with project/program delivery. Contributes and supports the Requirements Management / work packages for Tier 4-5 low risk and regulatory projects or initiatives Sound knowledge of business analysis, project delivery practices and standards across the project life-cycle Gain/acquire

Principal Regulatory Affairs Specialist (remote)

Medtronic

Remote or Los Angeles, California, USA

Full-time

Careers that Change Lives Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's w

Senior Regulatory Affairs Specialist (Medical Devices)

ApTask

Remote

Contract

Job Title: Senior Regulatory Affairs Specialist (Medical Devices) Location: Remote Duration: Long term contract Job Description: -Subject Matter Expert for Class II and Class 510(K) submission. -Hands on experience with 510(k) authoring, submissions, and communicating with the FDA. -Hands on experience with software as a Medical Device (SaMD) and validation requirements and applicable consensus standards. Key Responsibilities- -Authoring US FDA 510(k) submission using eSTAR submission tool.

Principal Regulatory Affairs Specialist (Remote)

Medtronic

Remote or Los Angeles, California, USA

Full-time

Careers that Change Lives Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's w

SAP PRA Consultant (Regulatory Reporting)

Activesoft, Inc.

Remote

Contract, Third Party

SAP PRA Consultant (Regulatory Reporting )Occasional Travel to Houston TXJob Description:1) Revenue Accounting and Disbursement 2) Production Accounting :Gas Booking and contracting, allocation, Well level accounting for production 3) Regulatory Reporting govt and federal agency including annual reporting.