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Hackensack Meridian Health JFK University Medical Center Edison, New Jersey Hackensack Meridian Health (HMH) seeks a dynamic and experienced educational administrator to serve as the Assistant Chief Academic Officer (ACAO) at JFK University Medical Center. This is a premier opportunity to provi...

Job DescriptionSalary: Job Description: iCreditWorks, one of the fastest-growing FinTech platforms in the United States, offers innovative Point-of-Sale (POS) lending and digital payment technologies, including the first-in-market native mobile App that reinvents B2B/B2B2C lending. We seek a h...

Job Description Job Summary: The Director of Marketing will play a critical role in executing the commercial success of our allergy portfolio, including a potentially groundbreaking new treatment poised to reshape the standard of care for treatment of severe allergies/anaphylaxis. Reporting to t...

Job DescriptionThis is a remote position. This is a temporary x-month contracted 1099 position with no benefits.” We are seeking an experienced Quality Assurance (QA) Consultant to provide immediate support for the setup and quality oversight of a Post-Trial Access (PTA) or WTA (Without Treatmen...

Job Description Job Description Date 06/2025 Location 1300 Airport Road, North Brunswick NJ 08902 Title Associate, In-Process Quality Assurance MFG/PKG Department Quality Assurance Operation Support Reports to Quality Assurance Manager/ VP of QA FLSA (Exempt or Non-Exempt Non-Exempt ...

Job DescriptionJob Summary: The Intellectual Property (IP) will oversee all legal aspects related to patents, trademarks, copyrights, and trade secrets within the pharmaceutical sector. This role requires an individual with executive presence and strong patent & IP legal skills combined with a ha...

Job DescriptionAbout Vitalief Vitalief partners with Sites, Sponsors, and CROs to streamline research operations, reduce costs, and accelerate breakthroughs that improve patient care. We bring deep clinical research expertise together with practical, results-driven consulting to help organization...

Job Description Job Summary: We are seeking a highly experienced and strategic Director of Advertising, Promotional & Labeling to lead regulatory review of promotional and labeling materials for both prescription and over-the-counter (dietary supplement) products in our growing biotech portfolio...

Job DescriptionSalary: DOE - Provide desired salary QA Specialist Opening in Edison, NJ! We have an opening for a Quality Assurance Specialist in Edison, NJ; at a renowned skincare manufacturer.As a Quality Assurance Specialist, you will play a pivotal role in upholding superior quality and...

Job Description The Vice President, Sales will be a critical commercial leader, responsible for executing on the full commercial launch of Anaphylm® for patients with severe allergic reactions, including anaphylaxis. This role holds full accountability for sales’ execution—with direct impact on r...

Job DescriptionCompany Description LVMH’s Beauty activities benefit from exceptional dynamism that relies on both the longevity and development of key lines, and on the boldness of new creations. All are driven by the same values: a quest for excellence, creativity, innovation, and perfect mas...

Job Description Role Description: The QA Specialist is responsible for managing processes such as (Document Control and Corrective Action and Preventive Action) and conducting quality assurance auditsof the quality management system to ensure compliance with ISO 13485:2016 standard and applicabl...

Job Description Job Summary: We’re seeking a dynamic Brand Manager to support commercial strategy and execution for driving the commercial success of our allergy portfolio, including a potentially groundbreaking new treatment poised to reshape the standard of care for treatment of severe allergi...

The Regulatory Affairs Lead for the Tactical Implementation Team will lead the regulatory team responsible for the execution of regulatory activities across assigned programs and markets. In collaboration with regulatory strategists, act as regulatory point of contact for cross-functional teams t...

Europe, support of international product registrations and related regulatory affairs activities, including execution of procedures and systems designed to ensure that the product development process addresses all regulatory requirements as well. Responsibilities: This position is responsible for...

Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis; assessment for Annex 3 comparative table with reference EU Member States Manage execution / authoring and review of CMC documentation (Module 1, 2 and 3 / Part II) for life cycle management - post-approv...

Regulatory Operations/Affairs Manager.Onsite role New Brunswick, NJ Work Schedule: Mon - Fri, Business Hours The External Manufacturing Quality Organization is seeking to recruit a Manager, Regulatory Affairs who will report directly to the Associate Director, Regulatory Affairs and will be respo...

Responsible for understanding the regulatory landscape, assessing regulatory risk, and developing global filing strategies. Leadership Role For Global Regulatory Strategy. Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion diagnostic tests...

Responsibilities: The Sr GPRM works under limited supervision of the regulatory affairs (RA) program lead to develop and implement the global regulatory strategy for program(s) through development, registration and post approval in the assigned region(s).The Sr GPRM may act as subject matter expe...

Job Description Spectrum Vascular is a leading innovator in vascular access solutions, committed to delivering excellence and advancing patient care. As a key member of our team, the International Sales Support Associate will be responsible for supporting our International Direct and Distributer ...

Job Description Spectrum Vascular is a leading innovator in vascular access solutions, committed to delivering excellence and advancing patient care. As a key member of our team, the Global Customer Experience Analyst will be primarily responsible for monitoring the company's Electronic Data ...

Responsibilities: The Regulatory Affairs Associate, with minimal guidance prepares, reviews and submits high quality annual reports with FDA within Annual report timelines and in accordance with regulatory guidelines and applicable federal laws. With minimal guidance, ensure to compile and comple...

Regulatory Cmc Leadership And Strategy.This position is a key role that will provide regulatory CMC (RA CMC) leadership and strategy to achieve regulatory approvals in various countries.As a strategic function, RA CMC is required to collaborate closely with multiple functions within Insmed and wi...

The Director of Medical Affairs organizes and directs Medical Staff with the Hospital Administration, Chief Medical Officer, Joint Commission, and applicable Federal, State, Local regulatory agencies. Reports to the Vice President of Medical Affairs/Chief Medical Officer, for all work, and suppli...

Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases.Our most valuable resource is our employees, and everything we do is motivated by a patients-first mentality.We are dedicated to growing our team with talented indivi...

Adaptability, Business Systems, Change Management, Communication, Cross-Cultural Awareness, Data Management, Employee Training Programs, FDA Regulations, Management Process, Pharmacovigilance, Policy Implementation, Regulatory Affairs Compliance, Regulatory Compliance, Regulatory Labeling, Regula...

For the LVMH Beauty scope of brands, joining the Regulatory Affairs & External Relations team to lead the operational regulatory affairs team on cosmetics and OTC drugs. Identifying and actioning opportunities on operational regulatory affairs topics to drive our Beauty business on cosmetic and O...

Adaptability, Adaptability, Business Processes, Change Management, Communication, Cross-Cultural Awareness, Data Management, Drug Development, Employee Training Programs, FDA Regulations, Management Process, Pharmacovigilance, Policy Implementation, Process Improvements, Project Information Manag...