Regulatory Affairs Jobs in USA

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionPosition requires extensive Oncology global full service clinical trial management experience. Preference given to candidates who also have Cell/Gene Therapy experience. Please demonstrate these in your application to be con...

Who we are:Cosmetic Solutions is a leader in the development and manufacturing of scientifically proven innovative personal care products. With a focusonface body hair OTC and professional use formulations we create some of the most cost effective high quality and powerful products on the market.Pro...

Job DescriptionAre You Ready to Make It Happen at Mondelēz InternationalJoin our Mission to Lead the Future of Snacking. Make It With Pride. Job Description:The Sanitation Manager develops implements and oversees all Sanitation and Pest Control strategies of the company. This position is responsible...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

DescriptionAt Cheniere we provide the world with safe reliable energy. But more than that we provide opportunities for our talented employees to impact their communities every day. Our diversity is key to our continued success and forges a path where our culture supports greater equity and inclusion...

Primary Function of PositionThis role will support our global Cardiac Surgery Program. This role is a Director-level Regulatory Affairs leader who will work with business unit leaders clinical teams reimbursement teams to define and execute global cardiac regulatory strategy leads a cross-functional...

1. End-to-End CMC Leadership & Cross-Functional IntegrationCreate and execute against integrated cross-functional project plans leading the integrated CMC strategy.Translate program strategy into cohesive development manufacturing and supply plans with clear milestones and deliverables.Drive cross-f...

THE POSITION: Medical Information is a critically important customer-facing function that supports the safe and effective use of pharmaceutical company products by providing timely scientifically balanced evidence based non-promotional information in response to unsolicited requests from healthcare...

Capital Forecasting & Analysis Director Location: McLean VA (Hybrid) Compensation: $225K$250K base bonus long-term incentives Company: Confidential Financial Services Leader (Fortune-Scale Impact) About the Opportunity: Northwest Talent Solutions (NWTS) is partnering with a highly respected missio...

This role is a Principal Engineer position in the Drug Delivery Systems and Packaging (DDSP) department within CSL this role you will be responsible for bringing new Drug Delivery Systems through the development process. You will have considerable cross-functional interactions that include Quality...

Job Description:Industry: Financial Services - MortgageJob Category: Finance / Accounting - Financial Analysis / Research/Reporting At our company our mission of Making Home Possible is what motivates us and it s at the core of everything we do. Since our charter in 1970 we have made home possible...

Job Summary We are seeking an experienced Senior Engineer - Medical Device Development with strong hands-on expertise across the endtoend medical device product development lifecycle including design documentation verification & validation (V&V) and regulatory compliance. The ideal candidate will ha...

Primary Function of PositionThis role will support our global Cardiac Surgery Program. This role is a Director-level Regulatory Affairs leader who will work with business unit leaders clinical teams reimbursement teams to define and execute global cardiac regulatory strategy leads a cross-functional...

PurposeThe Associate Director Regulatory Affairs Chemistry Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients. Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions...

The Reporting Specialist I is responsible for executing all of the reporting in partnership with internal and external stakeholders. The individual will also partner with internal teams such as pharmacovigilance local in-country teams and the device quality assurance team to ensure the appropriate a...

The Reporting Specialist II is responsible for executing all of the reporting in partnership with internal and external stakeholders. The individual will also partner with internal teams such as pharmacovigilance local in-country teams and the device quality assurance team to ensure the appropriate...

Clinical Supply Strategy & PlanningDevelop and execute global clinical supply strategies across Phase 1Phase 3 clinical development programs.Translate clinical protocols and enrollment assumptions into supply forecasts and operational supply plans.Design supply strategies for complex trials includin...

Responsible for quality of assigned products which may include small molecule pharmaceuticals and/or biologics products combination products and medical devices to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local divisional and corpora...

Talent will be hired at a level commensurate with experience.This geography covers the following states: OH KY IN IA NE SD ND MN WI MI ILThe Rheumatology Thought Leader Liaison (TLL) will act as the face of the AbbVie Marketing team with our External Experts developing implementing and maintaining i...

DEKA Research & Development has an immediate opening for a Regulatory Affairs Project Manager to contribute to a dynamic medical device research and development environment. The individual in this high visibility role will have a significant and direct impact on the success of th...