Director, Safety, Regulatory and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device and cosmetic portfol...
The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives for labeling activities for drugs, devices and combination products in assigned therapeutic area(s). E...
The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives for labeling activities for drugs, devices and combination products in assigned therapeutic area(s). E...
Director, Safety, Regulatory and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device and cosmetic portfol...
Director, Safety, Regulatory and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device and cosmetic portfol...
The Director Regulatory Affairs Global Regulatory Lead, Global Regulatory Strategy, is responsible for developing and implementing global strategies to secure and maintain market approval for product(s) in the assigned therapeutic area. May lead the Labeling Regulatory Strategy Team (LRST), and serv...
The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives for labeling activities for drugs, devices and combination products in assigned therapeutic area(s). E...
As the Senior Director Regulatory Affairs, Advanced Surgery you will be responsible for global strategic direction and performance (strategy and execution) of the Regulatory Affairs (RA) function within the division including development, implementation and management of global regulatory strategies...
Director, Safety, Regulatory and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device and cosmetic portfol...
FinOps Program Manager Location: Riverwoods Illinois 60015 Setting: Hybrid W2 ContractDuration: 6 Months Pay rate: $60-$80In this role: • you will be responsible for assisting with the management of the FinOps practice across the entire organization. You will: • This role is critical in ensuring cus...
Responsible for a product(s) or products with multiple driver indications within a Therapeutic Area and supports the Manager (Global Regulatory Lead (GRL), Associate Director, or Director), in the development & execution of the regulatory strategy. Assures that regulatory strategies defined with...
Are you a compassionate leader eager to steer and elevate a crucial healthcare program? Join Encompass Health, the nation's largest inpatient rehabilitation company, as a Dialysis Program Manager. Dialysis Program Manager Career Opportunity. Recognized for your expertise as a Dialysis Program Ma...
Responsible for a product(s) or products with multiple driver indications within a Therapeutic Area and supports the Manager (Global Regulatory Lead (GRL), Associate Director, or Director), in the development & execution of the regulatory strategy. Assures that regulatory strategies defined with...
Support the development of the device regulatory strategy and provide device input into the preparation and maintenance of chemistry, manufacturing, and controls (CMC) device sections of regulatory submissions, responses to Agency questions for worldwide registration and lifecycle management for the...
The Executive Director reports to a Member Board of Directors (Village Managers, Mayors of the member communities) through a seven-member Executive Committee (Police Chief, Fire Chief, County Administrator, Mayors, Trustees, Village / City Managers of the member municipalities and agencies). Lake Co...
Executive Director is responsible for providing effective and inspiring leadership to the Health Department workforce,. Executive Director is an advocate for public health on a local level, as well as at the state and federal level. The Executive Director must be visible and accessible to the commun...
The American Society of Crime Laboratory Directors (ASCLD) is a nonprofit professional society of crime laboratory directors and forensic science managers dedicated to providing excellence in forensic science through leadership and innovation. The American Society of Crime Laboratory DirectorsJob Po...
The Principal Compliance Specialist Role will be responsible for compliance advisory activities specific to applicable regulatory requirements impacting the respective business line or corporate function. The Principal Compliance Advisory will facilitate compliance with established Compliance Manage...
Here’s how the job details align with your profile.Barrington Area Council on Aging Mission:.Are you the right candidate for this opportunity Make sure to read the full description below.Bacoa redefines aging by empowering older adults, their caregivers and families as they pursue vibrant, healthy l...
The Executive Director is responsible for providing effective and inspiring leadership to the Health Department workforce, while overseeing administrative, fiscal, information technology, behavioral health, medical, prevention and environmental health services, and all other human resource operation...
The International Regulatory Specialist is responsible for providing regulatory support to Rust-Oleum's international business. Be part of a regulatory team that supports a >. ...
Represents Global Regulatory Affairs at research and development meetings and presents agreed upon regulatory positions. Follows scientific arguments, identifies regulatory scientific data needs and regulatory issues with alignment of regulatory management. Provides regulatory support and guidance a...
Foster open, honest, transparent communications between senior leaders, mid-level managers and non-exempt team members in ways that enhance engagement and service to customers. You will report to the VP, Communications and Public Affairs and be expected to work in either Lake Forest or our Chicago, ...
As the Executive Director, Asset Protection Field Operations, you are an experienced proven leader with a deep operational knowledge of all retail store functions that could adversely impact profitability in our most complex and challenging markets. In addition to leading all aspects of Asset Protec...
Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements as well as staying awa...