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Director, Regulatory Advertising
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Manager Global Regulatory Affairs
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Regulatory Affairs Associate
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Ramboll Princeton, United States Full timeJob Description · Job locations: Arlington, VA, Princeton, NJ, and Syracuse, NY are preferred locations; Richmond, VA; Bowie, MD; Hunt Valley, MD, USA are options as well. · Are you eager to develop your excellence in an inclusive, collaborative, and empowering community? Are yo ...
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Associate, Regulatory Affairs
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Regulatory Affairs Associate
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director regulatory affairs
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TechSpace Solutions Princeton, United StatesJob Title: Global Regulatory Lead, Oncology, Global Regulatory Strategy & Policy (Associate Director) · Location: Princeton Pike - 50% onsite · Duration:12+ Months · JD: · Develop global regulatory strategy for Oncology products in development and through life cycle management ...
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Associate, Regulatory Affairs
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Sun Pharmaceuticals, Inc Princeton, United StatesThe Associate, Regulatory Affairs - Labeling position is responsible for the preparation of various regulatory Labeling submissions. · **Area of Responsibility:** · 1. Review and timely completion of labeling for ANDA dossiers for submissions and prepare and review response to la ...
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Director Regulatory Affairs
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Lynkx Staffing LLC Princeton, United StatesJob Description · Job DescriptionOur Pharmaceutical client is seeking a Director Regulatory Affairs Chemistry Manufacturing & Controls (CMC) to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development pro ...
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Director, Regulatory Advertising
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Senior Regulatory Affairs
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Diverse Lynx Princeton, United StatesHi, · Welcome to Diverse Lynx We combine industry leading expertise and our personal dedication to help you find your next career opportunity. We are a Minority and Women Owned Business Enterprise (MWBE) certified by the State of New Jersey and Minority Business Enterprise (MBE) ...
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Bristol Myers Squibb Princeton, United States Full timeWorking with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production li ...
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Director Regulatory Affairs Strategy
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associate ii regulatory labeling
1 week ago
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USA - Regulatory Affairs Associate
1 week ago
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senior manager regulatory affairs
1 week ago
TK-CHAIN LLC Princeton, United StatesSUMMARY OF POSITION The Sr. Manager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Clients s drug development programs, policies and procedures; ensuring a co ...
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senior manager regulatory affairs
1 day ago
TK-CHAIN LLC Princeton, United StatesJob Description · Job DescriptionSUMMARY OF POSITION · The Sr. Manager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Clients s drug development programs, pol ...
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Senior Manager, Regulatory Affairs
4 days ago
Sun Pharma (Taro Pharma) Princeton, NJ, United StatesCOME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE · Hybrid work arrangement · Medical, Dental, Vision Benefits · Health Savings Account (HSA), Flexible Spending Account (FSA) · Prescription Drug Coverage · Telehealth and Behavior Health Services · Income Protectio ...
BA with Regulatory in Princeton, NJ - Zodiac Solutions
Description
Job Description
Job DescriptionHi
This is Nida Tahseen from Zodiac solutions Inc , I have got interesting Job opportunities across the USA .Below is the Job Description ,if you are looking a job change kindly share your resume .
Job Location/Client Location (with City & State) : Princeton, NJ (Hybrid Mode)
Job Title/Role BA with Regulatory experience
Mandatory Skills Business Analyst with Regulatory experience; GxP process experience required.
Client Interview Needed for Selection (Yes / No): Yes
Relocation : MUST in NJ
General Requirements:
7+ years of experience as BA
Working knowledge of Pharmaceutical R&D Life Sciences
Specific knowledge of Global Regulatory Affairs, submission content management and publishing, and Generis CARA product preferred
Knowledge of GxP processes is required for the role
Ability to work independently and with team
Detail oriented and strong communication skills
Ability to raise challenges/ concerns early and develop mitigation strategies to address
Comfortable working in a fast-paced, team-based environment
Nida Tahseen
Sales Account Manager
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Contact Details : |